NM_001291303.3(FAT4):c.7199+29T>G
|
rs7656135
|
0.99289
|
NM_001291303.3(FAT4):c.7707G>C (p.Val2569=)
|
rs988863
|
0.99289
|
NM_001291303.3(FAT4):c.7451-155C>T
|
rs4834041
|
0.99284
|
NM_001291303.3(FAT4):c.5921-61G>C
|
rs4605670
|
0.99275
|
NM_001291303.3(FAT4):c.11624G>A (p.Ser3875Asn)
|
rs12650153
|
0.99272
|
NM_001291303.3(FAT4):c.6843+29G>T
|
rs10010000
|
0.99271
|
NM_001291303.3(FAT4):c.6843+196T>C
|
rs11098811
|
0.99169
|
NM_001291303.3(FAT4):c.5569+157G>A
|
rs4508902
|
0.99033
|
NM_001291303.3(FAT4):c.5569+266T>C
|
rs6833240
|
0.99031
|
NM_001291303.3(FAT4):c.5760T>C (p.Asp1920=)
|
rs958415
|
0.99029
|
NM_001291303.3(FAT4):c.6844-48A>G
|
rs7675556
|
0.99028
|
NM_001291303.3(FAT4):c.7199+264T>A
|
rs7656590
|
0.98957
|
NM_001291303.3(FAT4):c.7199+155A>G
|
rs7678076
|
0.98936
|
NM_001291303.3(FAT4):c.5176-188G>A
|
rs1509295
|
0.98782
|
NM_001291303.3(FAT4):c.7450+288C>T
|
rs10084892
|
0.80450
|
NM_001291303.3(FAT4):c.12480-71G>T
|
rs1506361
|
0.75488
|
NM_001291303.3(FAT4):c.12213+128A>G
|
rs34321538
|
0.75382
|
NM_001291303.3(FAT4):c.2944T>C (p.Leu982=)
|
rs2940779
|
0.74871
|
NM_001291303.3(FAT4):c.14604A>G (p.Arg4868=)
|
rs1014866
|
0.74715
|
NM_001291303.3(FAT4):c.4305C>T (p.Ile1435=)
|
rs2710555
|
0.73896
|
NM_001291303.3(FAT4):c.12605-102C>T
|
rs10026056
|
0.56301
|
NM_001291303.3(FAT4):c.2420C>T (p.Ala807Val)
|
rs1039808
|
0.46652
|
NM_001291303.3(FAT4):c.11801-123C>T
|
rs4146009
|
0.41117
|
NM_001291303.3(FAT4):c.11905+83A>C
|
rs10010645
|
0.41034
|
NM_001291303.3(FAT4):c.12300-176G>A
|
rs10518467
|
0.38761
|
NM_001291303.3(FAT4):c.12604+306T>C
|
rs11737550
|
0.38701
|
NM_001291303.3(FAT4):c.12213+36A>G
|
rs35304021
|
0.38681
|
NM_001291303.3(FAT4):c.12213+48A>G
|
rs34927272
|
0.38662
|
NM_001291303.3(FAT4):c.12214-5C>T
|
rs17009761
|
0.38645
|
NM_001291303.3(FAT4):c.12214-270C>T
|
rs67399037
|
0.36725
|
NM_001291303.3(FAT4):c.13084+219A>T
|
rs1395237
|
0.36567
|
NM_001291303.3(FAT4):c.12213+207C>T
|
rs17009745
|
0.34179
|
NM_001291303.3(FAT4):c.12822+28T>G
|
rs11098815
|
0.34175
|
NM_001291303.3(FAT4):c.-13+109A>G
|
rs7677005
|
0.30700
|
NM_001291303.3(FAT4):c.12605-58C>T
|
rs10026069
|
0.23258
|
NM_001291303.3(FAT4):c.10577G>A (p.Gly3526Asp)
|
rs1567047
|
0.21721
|
NM_001291303.3(FAT4):c.13084+227G>C
|
rs1395236
|
0.21186
|
NM_001291303.3(FAT4):c.13623G>A (p.Glu4541=)
|
rs62312781
|
0.19007
|
NM_001291303.3(FAT4):c.405C>T (p.Phe135=)
|
rs72928772
|
0.17506
|
NM_001291303.3(FAT4):c.6585T>C (p.Asn2195=)
|
rs17009618
|
0.14565
|
NM_001291303.3(FAT4):c.5570-73C>G
|
rs10518464
|
0.13178
|
NM_001291303.3(FAT4):c.9649C>T (p.His3217Tyr)
|
rs73849225
|
0.12573
|
NM_001291303.3(FAT4):c.5176-167G>T
|
rs11736643
|
0.10585
|
NM_001291303.3(FAT4):c.3687G>C (p.Val1229=)
|
rs7657251
|
0.09845
|
NM_001291303.3(FAT4):c.12819G>A (p.Val4273=)
|
rs6824160
|
0.09773
|
NM_001291303.3(FAT4):c.12909C>T (p.Asp4303=)
|
rs17009825
|
0.08824
|
NM_001291303.3(FAT4):c.7451-62C>T
|
rs115240175
|
0.06887
|
NM_001291303.3(FAT4):c.7019-230T>G
|
rs17009654
|
0.06435
|
NM_001291303.3(FAT4):c.5176-82C>T
|
rs11946554
|
0.06217
|
NM_001291303.3(FAT4):c.3769C>G (p.Gln1257Glu)
|
rs36052762
|
0.05186
|
NM_001291303.3(FAT4):c.14920C>T (p.Pro4974Ser)
|
rs1014867
|
0.04974
|
NM_001291303.3(FAT4):c.12604+62C>T
|
rs17009769
|
0.04893
|
NM_001291303.3(FAT4):c.12480-300A>G
|
rs71585415
|
0.04890
|
NM_001291303.3(FAT4):c.12214-268C>T
|
rs75441829
|
0.04822
|
NM_001291303.3(FAT4):c.6844-276C>G
|
rs74829391
|
0.04515
|
NM_001291303.3(FAT4):c.12479+228_12479+231dup
|
rs78521593
|
0.04460
|
NM_001291303.3(FAT4):c.5176-276A>G
|
rs10009284
|
0.04154
|
NM_001291303.3(FAT4):c.11405C>T (p.Ser3802Phe)
|
rs75380987
|
0.03221
|
NM_001291303.3(FAT4):c.11905+228A>G
|
rs115142900
|
0.02719
|
NM_001291303.3(FAT4):c.11820A>G (p.Ser3940=)
|
rs17009721
|
0.02714
|
NM_001291303.3(FAT4):c.11800+290T>C
|
rs111403863
|
0.02708
|
NM_001291303.3(FAT4):c.12299+100G>A
|
rs17009763
|
0.02493
|
NM_001291303.3(FAT4):c.12605-231T>C
|
rs17009788
|
0.02490
|
NM_001291303.3(FAT4):c.12213+196A>G
|
rs17009741
|
0.02485
|
NM_001291303.3(FAT4):c.12852C>T (p.Ser4284=)
|
rs17009819
|
0.02466
|
NM_001291303.3(FAT4):c.12479+76G>T
|
rs75011900
|
0.02456
|
NM_001291303.3(FAT4):c.11488A>G (p.Lys3830Glu)
|
rs17009684
|
0.02342
|
NM_001291303.3(FAT4):c.7199+91C>T
|
rs80234380
|
0.02324
|
NM_001291303.3(FAT4):c.12214-72G>A
|
rs35472819
|
0.02315
|
NM_001291303.3(FAT4):c.5920+118A>C
|
rs12510547
|
0.02290
|
NM_001291303.3(FAT4):c.8482G>A (p.Asp2828Asn)
|
rs12508222
|
0.02049
|
NM_001291303.3(FAT4):c.14361C>T (p.Val4787=)
|
rs1014865
|
0.01862
|
NM_001291303.3(FAT4):c.14183G>A (p.Arg4728Lys)
|
rs72675395
|
0.01656
|
NM_001291303.3(FAT4):c.8592G>A (p.Val2864=)
|
rs111758803
|
0.01583
|
NM_001291303.3(FAT4):c.1101A>G (p.Val367=)
|
rs57692448
|
0.01498
|
NM_001291303.3(FAT4):c.14135C>G (p.Ser4712Cys)
|
rs147662558
|
0.01304
|
NM_001291303.3(FAT4):c.9876G>A (p.Gly3292=)
|
rs115219562
|
0.01168
|
NM_001291303.3(FAT4):c.8842A>G (p.Ile2948Val)
|
rs76048257
|
0.01112
|
NM_001291303.3(FAT4):c.13605G>A (p.Lys4535=)
|
rs75469760
|
0.01048
|
NM_001291303.3(FAT4):c.5921-122C>T
|
rs72914914
|
0.00999
|
NM_001291303.3(FAT4):c.10810A>C (p.Ile3604Leu)
|
rs76491994
|
0.00978
|
NM_001291303.3(FAT4):c.3096A>G (p.Ala1032=)
|
rs57537930
|
0.00811
|
NM_001291303.3(FAT4):c.8544C>T (p.Ser2848=)
|
rs139132509
|
0.00802
|
NM_001291303.3(FAT4):c.6844-291T>C
|
rs115421593
|
0.00797
|
NM_001291303.3(FAT4):c.12299+52T>C
|
rs115877455
|
0.00791
|
NM_001291303.3(FAT4):c.11801-332T>C
|
rs80253507
|
0.00760
|
NM_001291303.3(FAT4):c.11429A>G (p.His3810Arg)
|
rs114637892
|
0.00732
|
NM_001291303.3(FAT4):c.12071G>A (p.Arg4024Gln)
|
rs28515675
|
0.00726
|
NM_001291303.3(FAT4):c.12506C>T (p.Thr4169Ile)
|
rs115822434
|
0.00726
|
NM_001291303.3(FAT4):c.4154T>C (p.Leu1385Ser)
|
rs139883132
|
0.00597
|
NM_001291303.3(FAT4):c.14663C>G (p.Ala4888Gly)
|
rs35340865
|
0.00551
|
NM_001291303.3(FAT4):c.6219A>G (p.Gln2073=)
|
rs35355603
|
0.00545
|
NM_001291303.3(FAT4):c.6478A>G (p.Lys2160Glu)
|
rs75942329
|
0.00540
|
NM_001291303.3(FAT4):c.12986A>G (p.Asp4329Gly)
|
rs114234553
|
0.00519
|
NM_001291303.3(FAT4):c.10158A>G (p.Ala3386=)
|
rs144585931
|
0.00489
|
NM_001291303.3(FAT4):c.11801-128T>C
|
rs147095064
|
0.00487
|
NM_001291303.3(FAT4):c.11801-285T>C
|
rs192334885
|
0.00469
|
NM_001291303.3(FAT4):c.5921-23T>A
|
rs374890941
|
0.00466
|
NM_001291303.3(FAT4):c.14688C>T (p.His4896=)
|
rs35862879
|
0.00460
|
NM_001291303.3(FAT4):c.12213+130A>G
|
rs77364073
|
0.00432
|
NM_001291303.3(FAT4):c.12605-165A>G
|
rs140903503
|
0.00430
|
NM_001291303.3(FAT4):c.6733G>A (p.Val2245Ile)
|
rs112971995
|
0.00426
|
NM_001291303.3(FAT4):c.10853C>T (p.Thr3618Met)
|
rs111423173
|
0.00407
|
NM_001291303.3(FAT4):c.7200-312T>A
|
rs191546349
|
0.00397
|
NM_001291303.3(FAT4):c.5920+260G>A
|
rs116805434
|
0.00385
|
NM_001291303.3(FAT4):c.9891G>A (p.Val3297=)
|
rs139704889
|
0.00375
|
NM_001291303.3(FAT4):c.2811G>T (p.Lys937Asn)
|
rs112454576
|
0.00367
|
NM_001291303.3(FAT4):c.12855T>C (p.Asp4285=)
|
rs78040862
|
0.00365
|
NM_001291303.3(FAT4):c.3658T>A (p.Ser1220Thr)
|
rs181368820
|
0.00342
|
NM_001291303.3(FAT4):c.12070C>T (p.Arg4024Trp)
|
rs138019311
|
0.00333
|
NM_001291303.3(FAT4):c.7358G>T (p.Ser2453Ile)
|
rs72914988
|
0.00327
|
NM_001291303.3(FAT4):c.4303A>G (p.Ile1435Val)
|
rs142747281
|
0.00288
|
NM_001291303.3(FAT4):c.13554G>A (p.Leu4518=)
|
rs78235204
|
0.00277
|
NM_001291303.3(FAT4):c.14666G>A (p.Arg4889Lys)
|
rs35845544
|
0.00261
|
NM_001291303.3(FAT4):c.7935C>T (p.Asp2645=)
|
rs146157250
|
0.00244
|
NM_001291303.3(FAT4):c.5987A>G (p.Lys1996Arg)
|
rs140055438
|
0.00242
|
NM_001291303.3(FAT4):c.10390A>G (p.Ile3464Val)
|
rs147872710
|
0.00237
|
NM_001291303.3(FAT4):c.1128G>A (p.Val376=)
|
rs202216461
|
0.00236
|
NM_001291303.3(FAT4):c.14159C>G (p.Ala4720Gly)
|
rs76607227
|
0.00217
|
NM_001291303.3(FAT4):c.524G>T (p.Arg175Leu)
|
rs143534324
|
0.00217
|
NM_001291303.3(FAT4):c.7787T>C (p.Leu2596Ser)
|
rs111501860
|
0.00216
|
NM_001291303.3(FAT4):c.5176-31C>T
|
rs10033970
|
0.00199
|
NM_001291303.3(FAT4):c.13404G>A (p.Val4468=)
|
rs149993049
|
0.00181
|
NM_001291303.3(FAT4):c.831G>A (p.Ala277=)
|
rs142490028
|
0.00175
|
NM_001291303.3(FAT4):c.4839G>A (p.Ser1613=)
|
rs180866934
|
0.00164
|
NM_001291303.3(FAT4):c.5921-14C>T
|
rs190218898
|
0.00151
|
NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val)
|
rs145639192
|
0.00145
|
NM_001291303.3(FAT4):c.10107A>G (p.Glu3369=)
|
rs147646369
|
0.00140
|
NM_001291303.3(FAT4):c.3294T>A (p.Pro1098=)
|
rs200300207
|
0.00140
|
NM_001291303.3(FAT4):c.3424G>A (p.Val1142Met)
|
rs202188213
|
0.00140
|
NM_001291303.3(FAT4):c.4219G>A (p.Val1407Ile)
|
rs114227532
|
0.00133
|
NM_001291303.3(FAT4):c.3192C>T (p.Asp1064=)
|
rs140899478
|
0.00132
|
NM_001291303.3(FAT4):c.12479+8G>A
|
rs150505878
|
0.00121
|
NM_001291303.3(FAT4):c.1855C>T (p.Arg619Cys)
|
rs202125547
|
0.00121
|
NM_001291303.3(FAT4):c.8021A>T (p.Asp2674Val)
|
rs138655269
|
0.00121
|
NM_001291303.3(FAT4):c.3402A>T (p.Glu1134Asp)
|
rs144768563
|
0.00113
|
NM_001291303.3(FAT4):c.9828C>T (p.Pro3276=)
|
rs73849226
|
0.00106
|
NM_001291303.3(FAT4):c.7052A>G (p.Asn2351Ser)
|
rs145105421
|
0.00096
|
NM_001291303.3(FAT4):c.11619C>T (p.Cys3873=)
|
rs141328606
|
0.00092
|
NM_001291303.3(FAT4):c.7231A>T (p.Thr2411Ser)
|
rs147297895
|
0.00091
|
NM_001291303.3(FAT4):c.14940A>G (p.Glu4980=)
|
rs149073729
|
0.00088
|
NM_001291303.3(FAT4):c.10635C>G (p.Pro3545=)
|
rs181032092
|
0.00087
|
NM_001291303.3(FAT4):c.12713C>T (p.Ala4238Val)
|
rs183396105
|
0.00087
|
NM_001291303.3(FAT4):c.3682C>G (p.Gln1228Glu)
|
rs200227715
|
0.00087
|
NM_001291303.3(FAT4):c.11670C>T (p.Cys3890=)
|
rs150894545
|
0.00086
|
NM_001291303.3(FAT4):c.2919C>T (p.Val973=)
|
rs144356360
|
0.00083
|
NM_001291303.3(FAT4):c.3962T>C (p.Phe1321Ser)
|
rs147900577
|
0.00070
|
NM_001291303.3(FAT4):c.11693C>T (p.Ala3898Val)
|
rs138275098
|
0.00069
|
NM_001291303.3(FAT4):c.7103C>A (p.Ala2368Glu)
|
rs116568645
|
0.00066
|
NM_001291303.3(FAT4):c.9810G>A (p.Val3270=)
|
rs139518045
|
0.00062
|
NM_001291303.3(FAT4):c.11260A>G (p.Ser3754Gly)
|
rs79909102
|
0.00061
|
NM_001291303.3(FAT4):c.2475C>T (p.Asn825=)
|
rs764273048
|
0.00061
|
NM_001291303.3(FAT4):c.5792A>G (p.Tyr1931Cys)
|
rs139716832
|
0.00061
|
NM_001291303.3(FAT4):c.12769G>A (p.Glu4257Lys)
|
rs143513466
|
0.00056
|
NM_001291303.3(FAT4):c.13111A>G (p.Met4371Val)
|
rs139260545
|
0.00056
|
NM_001291303.3(FAT4):c.13555G>A (p.Ala4519Thr)
|
rs202148971
|
0.00055
|
NM_001291303.3(FAT4):c.8290A>C (p.Asn2764His)
|
rs147281598
|
0.00051
|
NM_001291303.3(FAT4):c.131A>C (p.Glu44Ala)
|
rs200221425
|
0.00049
|
NM_001291303.3(FAT4):c.12342C>G (p.Ile4114Met)
|
rs150804471
|
0.00048
|
NM_001291303.3(FAT4):c.13417G>A (p.Val4473Ile)
|
rs145835705
|
0.00048
|
NM_001291303.3(FAT4):c.10560G>A (p.Met3520Ile)
|
rs144506470
|
0.00047
|
NM_001291303.3(FAT4):c.4199G>A (p.Arg1400His)
|
rs376791829
|
0.00047
|
NM_001291303.3(FAT4):c.185G>C (p.Gly62Ala)
|
rs201009019
|
0.00045
|
NM_001291303.3(FAT4):c.2917G>A (p.Val973Ile)
|
rs199497561
|
0.00044
|
NM_001291303.3(FAT4):c.9602A>G (p.Tyr3201Cys)
|
rs115895451
|
0.00044
|
NM_001291303.3(FAT4):c.3768A>G (p.Arg1256=)
|
rs114652326
|
0.00042
|
NM_001291303.3(FAT4):c.12647G>A (p.Arg4216His)
|
rs148170326
|
0.00041
|
NM_001291303.3(FAT4):c.13460C>T (p.Ala4487Val)
|
rs141234678
|
0.00040
|
NM_001291303.3(FAT4):c.12066C>T (p.Gly4022=)
|
rs144476127
|
0.00036
|
NM_001291303.3(FAT4):c.7053C>T (p.Asn2351=)
|
rs199682494
|
0.00036
|
NM_001291303.3(FAT4):c.5367C>T (p.Ile1789=)
|
rs144922340
|
0.00035
|
NM_001291303.3(FAT4):c.5552C>T (p.Pro1851Leu)
|
rs138655912
|
0.00035
|
NM_001291303.3(FAT4):c.10570C>T (p.Arg3524Trp)
|
rs145569482
|
0.00034
|
NM_001291303.3(FAT4):c.1419T>C (p.Pro473=)
|
rs199637020
|
0.00034
|
NM_001291303.3(FAT4):c.5054G>A (p.Arg1685Gln)
|
rs376422522
|
0.00034
|
NM_001291303.3(FAT4):c.1698C>T (p.Ala566=)
|
rs370653820
|
0.00033
|
NM_001291303.3(FAT4):c.3642T>G (p.Phe1214Leu)
|
rs201264765
|
0.00033
|
NM_001291303.3(FAT4):c.4432A>C (p.Ile1478Leu)
|
rs200565115
|
0.00033
|
NM_001291303.3(FAT4):c.5597C>T (p.Thr1866Met)
|
rs141773516
|
0.00033
|
NM_001291303.3(FAT4):c.10392C>A (p.Ile3464=)
|
rs140494092
|
0.00032
|
NM_001291303.3(FAT4):c.13206C>A (p.Gly4402=)
|
rs200101519
|
0.00032
|
NM_001291303.3(FAT4):c.8055C>T (p.Ser2685=)
|
rs139033158
|
0.00032
|
NM_001291303.3(FAT4):c.14718C>T (p.Gly4906=)
|
rs147617723
|
0.00030
|
NM_001291303.3(FAT4):c.6731C>T (p.Thr2244Met)
|
rs145342353
|
0.00030
|
NM_001291303.3(FAT4):c.3049A>G (p.Lys1017Glu)
|
rs200995117
|
0.00029
|
NM_001291303.3(FAT4):c.8854A>C (p.Ser2952Arg)
|
rs538489921
|
0.00029
|
NM_001291303.3(FAT4):c.10461A>T (p.Ser3487=)
|
rs79482316
|
0.00028
|
NM_001291303.3(FAT4):c.3120A>G (p.Thr1040=)
|
rs202128638
|
0.00028
|
NM_001291303.3(FAT4):c.3417T>C (p.Phe1139=)
|
rs367935912
|
0.00027
|
NM_001291303.3(FAT4):c.11040G>A (p.Thr3680=)
|
rs147998041
|
0.00026
|
NM_001291303.3(FAT4):c.8580C>T (p.Val2860=)
|
rs144031841
|
0.00026
|
NM_001291303.3(FAT4):c.13029T>C (p.Leu4343=)
|
rs146822665
|
0.00025
|
NM_001291303.3(FAT4):c.5883T>C (p.Ser1961=)
|
rs117016099
|
0.00025
|
NM_001291303.3(FAT4):c.8078C>T (p.Ser2693Leu)
|
rs148918820
|
0.00025
|
NM_001291303.3(FAT4):c.12321T>C (p.Asn4107=)
|
rs200344963
|
0.00024
|
NM_001291303.3(FAT4):c.9141C>T (p.Ser3047=)
|
rs146492311
|
0.00024
|
NM_001291303.3(FAT4):c.11378T>C (p.Leu3793Pro)
|
rs149757393
|
0.00023
|
NM_001291303.3(FAT4):c.14388G>A (p.Arg4796=)
|
rs149584153
|
0.00023
|
NM_001291303.3(FAT4):c.7196T>C (p.Ile2399Thr)
|
rs140285782
|
0.00023
|
NM_001291303.3(FAT4):c.1296T>C (p.Pro432=)
|
rs372007282
|
0.00022
|
NM_001291303.3(FAT4):c.12108A>G (p.Arg4036=)
|
rs199730809
|
0.00021
|
NM_001291303.3(FAT4):c.14875G>A (p.Ala4959Thr)
|
rs553653311
|
0.00021
|
NM_001291303.3(FAT4):c.14877A>G (p.Ala4959=)
|
rs376402724
|
0.00021
|
NM_001291303.3(FAT4):c.1959C>T (p.Ala653=)
|
rs191491571
|
0.00021
|
NM_001291303.3(FAT4):c.4941C>T (p.Asn1647=)
|
rs184884584
|
0.00021
|
NM_001291303.3(FAT4):c.6640G>A (p.Ala2214Thr)
|
rs149686118
|
0.00021
|
NM_001291303.3(FAT4):c.829G>A (p.Ala277Thr)
|
rs183191959
|
0.00021
|
NM_001291303.3(FAT4):c.11380C>T (p.Arg3794Trp)
|
rs201859188
|
0.00020
|
NM_001291303.3(FAT4):c.10035G>T (p.Lys3345Asn)
|
rs200721145
|
0.00019
|
NM_001291303.3(FAT4):c.12032C>T (p.Ala4011Val)
|
rs149250709
|
0.00019
|
NM_001291303.3(FAT4):c.12777C>T (p.Gly4259=)
|
rs558612271
|
0.00019
|
NM_001291303.3(FAT4):c.1432C>G (p.Gln478Glu)
|
rs201892240
|
0.00019
|
NM_001291303.3(FAT4):c.7452T>C (p.Gly2484=)
|
rs200513521
|
0.00019
|
NM_001291303.3(FAT4):c.761A>T (p.His254Leu)
|
rs201036193
|
0.00019
|
NM_001291303.3(FAT4):c.7798C>T (p.Pro2600Ser)
|
rs146482628
|
0.00019
|
NM_001291303.3(FAT4):c.8812C>A (p.Gln2938Lys)
|
rs370499753
|
0.00019
|
NM_001291303.3(FAT4):c.8821A>G (p.Thr2941Ala)
|
rs151209952
|
0.00019
|
NM_001291303.3(FAT4):c.8343C>A (p.Ala2781=)
|
rs141532188
|
0.00018
|
NM_001291303.3(FAT4):c.3212T>C (p.Val1071Ala)
|
rs200138872
|
0.00017
|
NM_001291303.3(FAT4):c.6977C>T (p.Thr2326Ile)
|
rs200344386
|
0.00017
|
NM_001291303.3(FAT4):c.7079A>G (p.Asn2360Ser)
|
rs534302520
|
0.00017
|
NM_001291303.3(FAT4):c.8731T>C (p.Tyr2911His)
|
rs148655455
|
0.00017
|
NM_001291303.3(FAT4):c.9627C>T (p.Ala3209=)
|
rs148558216
|
0.00017
|
NM_001291303.3(FAT4):c.2322C>T (p.Pro774=)
|
rs200593370
|
0.00016
|
NM_001291303.3(FAT4):c.4169T>C (p.Ile1390Thr)
|
rs201934636
|
0.00016
|
NM_001291303.3(FAT4):c.10643A>G (p.Tyr3548Cys)
|
rs79726583
|
0.00015
|
NM_001291303.3(FAT4):c.10839T>C (p.Pro3613=)
|
rs143871901
|
0.00015
|
NM_001291303.3(FAT4):c.11906-10C>T
|
rs370757220
|
0.00015
|
NM_001291303.3(FAT4):c.3958C>A (p.Leu1320Ile)
|
rs551446826
|
0.00015
|
NM_001291303.3(FAT4):c.5311G>A (p.Ala1771Thr)
|
rs147751409
|
0.00015
|
NM_001291303.3(FAT4):c.6094A>G (p.Thr2032Ala)
|
rs147314754
|
0.00015
|
NM_001291303.3(FAT4):c.11153G>A (p.Arg3718His)
|
rs139635339
|
0.00014
|
NM_001291303.3(FAT4):c.11822T>C (p.Val3941Ala)
|
rs578140620
|
0.00014
|
NM_001291303.3(FAT4):c.13802C>T (p.Pro4601Leu)
|
rs200851934
|
0.00014
|
NM_001291303.3(FAT4):c.4000G>A (p.Val1334Met)
|
rs368607709
|
0.00014
|
NM_001291303.3(FAT4):c.4953A>G (p.Ile1651Met)
|
rs201688197
|
0.00014
|
NM_001291303.3(FAT4):c.6970C>T (p.Arg2324Trp)
|
rs559079176
|
0.00014
|
NM_001291303.3(FAT4):c.7131A>G (p.Ala2377=)
|
rs138403046
|
0.00014
|
NM_001291303.3(FAT4):c.9083A>G (p.Asp3028Gly)
|
rs765151671
|
0.00014
|
NM_001291303.3(FAT4):c.9975C>T (p.Ser3325=)
|
rs374971295
|
0.00014
|
NM_001291303.3(FAT4):c.1099G>A (p.Val367Ile)
|
rs747531733
|
0.00013
|
NM_001291303.3(FAT4):c.12851C>T (p.Ser4284Phe)
|
rs199682210
|
0.00013
|
NM_001291303.3(FAT4):c.13878C>T (p.Asn4626=)
|
rs369989432
|
0.00013
|
NM_001291303.3(FAT4):c.14325G>A (p.Pro4775=)
|
rs758537642
|
0.00013
|
NM_001291303.3(FAT4):c.188C>T (p.Thr63Ile)
|
rs754711855
|
0.00013
|
NM_001291303.3(FAT4):c.2897T>C (p.Ile966Thr)
|
rs200952904
|
0.00013
|
NM_001291303.3(FAT4):c.390C>T (p.Asp130=)
|
rs373639016
|
0.00013
|
NM_001291303.3(FAT4):c.4549A>C (p.Ile1517Leu)
|
rs374899663
|
0.00013
|
NM_001291303.3(FAT4):c.5401C>T (p.Arg1801Trp)
|
rs201887525
|
0.00013
|
NM_001291303.3(FAT4):c.6732G>A (p.Thr2244=)
|
rs138078089
|
0.00013
|
NM_001291303.3(FAT4):c.12822+17T>C
|
rs1219112389
|
0.00012
|
NM_001291303.3(FAT4):c.13193T>C (p.Ile4398Thr)
|
rs200729108
|
0.00012
|
NM_001291303.3(FAT4):c.2985G>A (p.Val995=)
|
rs201226727
|
0.00012
|
NM_001291303.3(FAT4):c.7326G>A (p.Ala2442=)
|
rs201829586
|
0.00012
|
NM_001291303.3(FAT4):c.8313T>C (p.Asn2771=)
|
rs148344513
|
0.00012
|
NM_001291303.3(FAT4):c.12498C>T (p.Gly4166=)
|
rs190749052
|
0.00011
|
NM_001291303.3(FAT4):c.12716T>C (p.Met4239Thr)
|
rs137954725
|
0.00011
|
NM_001291303.3(FAT4):c.13388C>T (p.Thr4463Ile)
|
rs199971037
|
0.00011
|
NM_001291303.3(FAT4):c.14700C>T (p.Ala4900=)
|
rs149897030
|
0.00011
|
NM_001291303.3(FAT4):c.1470G>A (p.Pro490=)
|
rs377282354
|
0.00011
|
NM_001291303.3(FAT4):c.14935G>A (p.Ala4979Thr)
|
rs17009858
|
0.00011
|
NM_001291303.3(FAT4):c.4080C>T (p.His1360=)
|
rs371821589
|
0.00011
|
NM_001291303.3(FAT4):c.6050T>C (p.Val2017Ala)
|
rs188126059
|
0.00011
|
NM_001291303.3(FAT4):c.6435T>C (p.Leu2145=)
|
rs764905177
|
0.00011
|
NM_001291303.3(FAT4):c.7264A>T (p.Ser2422Cys)
|
rs139924242
|
0.00011
|
NM_001291303.3(FAT4):c.779C>T (p.Pro260Leu)
|
rs749582331
|
0.00011
|
NM_001291303.3(FAT4):c.7947T>G (p.Pro2649=)
|
rs375259992
|
0.00011
|
NM_001291303.3(FAT4):c.9451G>A (p.Ala3151Thr)
|
rs200702071
|
0.00011
|
NM_001291303.3(FAT4):c.11198T>C (p.Leu3733Pro)
|
rs145248395
|
0.00010
|
NM_001291303.3(FAT4):c.12778G>A (p.Val4260Ile)
|
rs369024765
|
0.00010
|
NM_001291303.3(FAT4):c.12853G>A (p.Asp4285Asn)
|
rs149301924
|
0.00010
|
NM_001291303.3(FAT4):c.13088G>T (p.Gly4363Val)
|
rs199797338
|
0.00010
|
NM_001291303.3(FAT4):c.3505C>T (p.Arg1169Trp)
|
rs190175933
|
0.00010
|
NM_001291303.3(FAT4):c.7266C>T (p.Ser2422=)
|
rs147010455
|
0.00010
|
NM_001291303.3(FAT4):c.9597T>A (p.Asp3199Glu)
|
rs568003396
|
0.00010
|
NM_001291303.3(FAT4):c.1098G>A (p.Ser366=)
|
rs374401618
|
0.00009
|
NM_001291303.3(FAT4):c.11905+18G>C
|
rs576051605
|
0.00009
|
NM_001291303.3(FAT4):c.12085G>A (p.Ala4029Thr)
|
rs140544054
|
0.00009
|
NM_001291303.3(FAT4):c.13179T>C (p.Asp4393=)
|
rs376657630
|
0.00009
|
NM_001291303.3(FAT4):c.13634C>T (p.Pro4545Leu)
|
rs200092854
|
0.00009
|
NM_001291303.3(FAT4):c.14362G>A (p.Gly4788Arg)
|
rs138173652
|
0.00009
|
NM_001291303.3(FAT4):c.14577G>A (p.Arg4859=)
|
rs144832106
|
0.00009
|
NM_001291303.3(FAT4):c.4998T>C (p.Tyr1666=)
|
rs754645745
|
0.00009
|
NM_001291303.3(FAT4):c.5415A>G (p.Glu1805=)
|
rs551837507
|
0.00009
|
NM_001291303.3(FAT4):c.5429A>T (p.Tyr1810Phe)
|
rs201947859
|
0.00009
|
NM_001291303.3(FAT4):c.6729C>T (p.Ser2243=)
|
rs368872163
|
0.00009
|
NM_001291303.3(FAT4):c.6976A>G (p.Thr2326Ala)
|
rs757774648
|
0.00009
|
NM_001291303.3(FAT4):c.6985C>T (p.Arg2329Cys)
|
rs148293496
|
0.00009
|
NM_001291303.3(FAT4):c.7312G>T (p.Val2438Phe)
|
rs376545643
|
0.00009
|
NM_001291303.3(FAT4):c.7813A>G (p.Ile2605Val)
|
rs745697037
|
0.00009
|
NM_001291303.3(FAT4):c.821C>T (p.Ala274Val)
|
rs199605036
|
0.00009
|
NM_001291303.3(FAT4):c.8537G>A (p.Arg2846Gln)
|
rs373393333
|
0.00009
|
NM_001291303.3(FAT4):c.9282C>T (p.Ser3094=)
|
rs773285768
|
0.00009
|
NM_001291303.3(FAT4):c.10994G>C (p.Gly3665Ala)
|
rs777960103
|
0.00008
|
NM_001291303.3(FAT4):c.13143C>T (p.Ser4381=)
|
rs755894084
|
0.00008
|
NM_001291303.3(FAT4):c.3675T>A (p.Asn1225Lys)
|
rs202235021
|
0.00008
|
NM_001291303.3(FAT4):c.6607C>T (p.Arg2203Trp)
|
rs374328795
|
0.00008
|
NM_001291303.3(FAT4):c.7147G>A (p.Val2383Ile)
|
rs143943210
|
0.00008
|
NM_001291303.3(FAT4):c.11358A>G (p.Glu3786=)
|
rs369625076
|
0.00007
|
NM_001291303.3(FAT4):c.11462G>A (p.Arg3821Gln)
|
rs142857910
|
0.00007
|
NM_001291303.3(FAT4):c.12358A>G (p.Ile4120Val)
|
rs372543077
|
0.00007
|
NM_001291303.3(FAT4):c.12381G>A (p.Val4127=)
|
rs377051363
|
0.00007
|
NM_001291303.3(FAT4):c.132G>A (p.Glu44=)
|
rs763601689
|
0.00007
|
NM_001291303.3(FAT4):c.1802A>G (p.Glu601Gly)
|
rs377156485
|
0.00007
|
NM_001291303.3(FAT4):c.3622C>T (p.Pro1208Ser)
|
rs761868141
|
0.00007
|
NM_001291303.3(FAT4):c.4797C>A (p.Leu1599=)
|
rs746466001
|
0.00007
|
NM_001291303.3(FAT4):c.6957A>G (p.Thr2319=)
|
rs201407156
|
0.00007
|
NM_001291303.3(FAT4):c.8636A>G (p.Tyr2879Cys)
|
rs781160819
|
0.00007
|
NM_001291303.3(FAT4):c.929C>A (p.Pro310His)
|
rs371090730
|
0.00007
|
NM_001291303.3(FAT4):c.9549C>T (p.Thr3183=)
|
rs775219647
|
0.00007
|
NM_001291303.3(FAT4):c.10336A>G (p.Ile3446Val)
|
rs756625118
|
0.00006
|
NM_001291303.3(FAT4):c.10571G>A (p.Arg3524Gln)
|
rs200082059
|
0.00006
|
NM_001291303.3(FAT4):c.10750C>G (p.Leu3584Val)
|
rs751277769
|
0.00006
|
NM_001291303.3(FAT4):c.10780C>T (p.Pro3594Ser)
|
rs374073545
|
0.00006
|
NM_001291303.3(FAT4):c.11906-17A>C
|
rs748245015
|
0.00006
|
NM_001291303.3(FAT4):c.12166G>T (p.Val4056Leu)
|
rs753998777
|
0.00006
|
NM_001291303.3(FAT4):c.1222G>A (p.Glu408Lys)
|
rs574924064
|
0.00006
|
NM_001291303.3(FAT4):c.12299+9T>C
|
rs552147348
|
0.00006
|
NM_001291303.3(FAT4):c.12499G>A (p.Ala4167Thr)
|
rs369432764
|
0.00006
|
NM_001291303.3(FAT4):c.1289G>A (p.Arg430His)
|
rs774644392
|
0.00006
|
NM_001291303.3(FAT4):c.13347C>T (p.Ser4449=)
|
rs758589643
|
0.00006
|
NM_001291303.3(FAT4):c.13635G>A (p.Pro4545=)
|
rs757657669
|
0.00006
|
NM_001291303.3(FAT4):c.13666G>A (p.Val4556Ile)
|
rs755666152
|
0.00006
|
NM_001291303.3(FAT4):c.14587A>G (p.Met4863Val)
|
rs200302369
|
0.00006
|
NM_001291303.3(FAT4):c.14678G>A (p.Arg4893Gln)
|
rs151139631
|
0.00006
|
NM_001291303.3(FAT4):c.2273C>T (p.Ala758Val)
|
rs570502199
|
0.00006
|
NM_001291303.3(FAT4):c.3067A>G (p.Lys1023Glu)
|
rs758101910
|
0.00006
|
NM_001291303.3(FAT4):c.3937C>T (p.Pro1313Ser)
|
rs748743944
|
0.00006
|
NM_001291303.3(FAT4):c.3939T>G (p.Pro1313=)
|
rs1045111379
|
0.00006
|
NM_001291303.3(FAT4):c.4069A>T (p.Thr1357Ser)
|
rs375109338
|
0.00006
|
NM_001291303.3(FAT4):c.4543G>A (p.Val1515Met)
|
rs773912269
|
0.00006
|
NM_001291303.3(FAT4):c.4706A>G (p.Asn1569Ser)
|
rs768412027
|
0.00006
|
NM_001291303.3(FAT4):c.5308-5T>C
|
rs373654898
|
0.00006
|
NM_001291303.3(FAT4):c.5530C>T (p.Pro1844Ser)
|
rs76963800
|
0.00006
|
NM_001291303.3(FAT4):c.6597T>C (p.Asn2199=)
|
rs377502295
|
0.00006
|
NM_001291303.3(FAT4):c.6639C>T (p.Val2213=)
|
rs759154801
|
0.00006
|
NM_001291303.3(FAT4):c.6917A>G (p.Asn2306Ser)
|
rs369144497
|
0.00006
|
NM_001291303.3(FAT4):c.7582G>A (p.Gly2528Arg)
|
rs199986451
|
0.00006
|
NM_001291303.3(FAT4):c.7963G>A (p.Glu2655Lys)
|
rs556536853
|
0.00006
|
NM_001291303.3(FAT4):c.8408T>C (p.Ile2803Thr)
|
rs745425307
|
0.00006
|
NM_001291303.3(FAT4):c.9981T>C (p.Arg3327=)
|
rs752677813
|
0.00006
|
NM_001291303.3(FAT4):c.10224A>G (p.Leu3408=)
|
rs761771089
|
0.00005
|
NM_001291303.3(FAT4):c.11309G>A (p.Arg3770Gln)
|
rs540725305
|
0.00005
|
NM_001291303.3(FAT4):c.1198G>T (p.Gly400Trp)
|
rs760281262
|
0.00005
|
NM_001291303.3(FAT4):c.12099C>T (p.Ala4033=)
|
rs774481338
|
0.00005
|
NM_001291303.3(FAT4):c.12910G>A (p.Gly4304Ser)
|
rs746761404
|
0.00005
|
NM_001291303.3(FAT4):c.13828G>A (p.Ala4610Thr)
|
rs142894845
|
0.00005
|
NM_001291303.3(FAT4):c.13893C>T (p.Ala4631=)
|
rs144900187
|
0.00005
|
NM_001291303.3(FAT4):c.14689G>A (p.Gly4897Ser)
|
rs370075940
|
0.00005
|
NM_001291303.3(FAT4):c.14693G>A (p.Arg4898His)
|
rs531333503
|
0.00005
|
NM_001291303.3(FAT4):c.1811T>G (p.Met604Arg)
|
rs376751408
|
0.00005
|
NM_001291303.3(FAT4):c.4250C>A (p.Pro1417His)
|
rs201515596
|
0.00005
|
NM_001291303.3(FAT4):c.4599C>T (p.Asn1533=)
|
rs371858685
|
0.00005
|
NM_001291303.3(FAT4):c.5307+40T>C
|
rs569179408
|
0.00005
|
NM_001291303.3(FAT4):c.5404T>C (p.Leu1802=)
|
rs191940938
|
0.00005
|
NM_001291303.3(FAT4):c.5806G>A (p.Asp1936Asn)
|
rs1235801879
|
0.00005
|
NM_001291303.3(FAT4):c.6324C>G (p.Leu2108=)
|
rs140302868
|
0.00005
|
NM_001291303.3(FAT4):c.6822A>T (p.Thr2274=)
|
rs192467233
|
0.00005
|
NM_001291303.3(FAT4):c.7240C>A (p.Pro2414Thr)
|
rs369092138
|
0.00005
|
NM_001291303.3(FAT4):c.7579G>A (p.Ala2527Thr)
|
rs201007539
|
0.00005
|
NM_001291303.3(FAT4):c.8525G>A (p.Arg2842His)
|
rs146180798
|
0.00005
|
NM_001291303.3(FAT4):c.8967A>G (p.Lys2989=)
|
rs374645878
|
0.00005
|
NM_001291303.3(FAT4):c.9163C>A (p.Gln3055Lys)
|
rs199778782
|
0.00005
|
NM_001291303.3(FAT4):c.9550G>A (p.Val3184Ile)
|
rs760921459
|
0.00005
|
NM_001291303.3(FAT4):c.10061C>A (p.Thr3354Asn)
|
rs145285004
|
0.00004
|
NM_001291303.3(FAT4):c.11725A>G (p.Ser3909Gly)
|
rs531337325
|
0.00004
|
NM_001291303.3(FAT4):c.11943A>T (p.Gly3981=)
|
rs754755525
|
0.00004
|
NM_001291303.3(FAT4):c.12214-4G>A
|
rs751996990
|
0.00004
|
NM_001291303.3(FAT4):c.1244C>G (p.Pro415Arg)
|
rs746792200
|
0.00004
|
NM_001291303.3(FAT4):c.12604+17G>A
|
rs563419094
|
0.00004
|
NM_001291303.3(FAT4):c.12768C>T (p.Ser4256=)
|
rs1006074076
|
0.00004
|
NM_001291303.3(FAT4):c.1299C>G (p.Ser433=)
|
rs764678411
|
0.00004
|
NM_001291303.3(FAT4):c.13202G>A (p.Arg4401His)
|
rs778549155
|
0.00004
|
NM_001291303.3(FAT4):c.13308G>A (p.Pro4436=)
|
rs763876721
|
0.00004
|
NM_001291303.3(FAT4):c.13374G>A (p.Ser4458=)
|
rs961260881
|
0.00004
|
NM_001291303.3(FAT4):c.13543G>A (p.Ala4515Thr)
|
rs369929089
|
0.00004
|
NM_001291303.3(FAT4):c.13837G>A (p.Ala4613Thr)
|
rs151087097
|
0.00004
|
NM_001291303.3(FAT4):c.13927C>G (p.Gln4643Glu)
|
rs370704263
|
0.00004
|
NM_001291303.3(FAT4):c.14138C>T (p.Thr4713Met)
|
rs770459923
|
0.00004
|
NM_001291303.3(FAT4):c.1420G>A (p.Val474Ile)
|
rs753978592
|
0.00004
|
NM_001291303.3(FAT4):c.14311C>T (p.Arg4771Cys)
|
rs144845192
|
0.00004
|
NM_001291303.3(FAT4):c.14530A>T (p.Ser4844Cys)
|
rs780522985
|
0.00004
|
NM_001291303.3(FAT4):c.1587C>T (p.Ser529=)
|
rs770456067
|
0.00004
|
NM_001291303.3(FAT4):c.1830G>A (p.Gly610=)
|
rs774467641
|
0.00004
|
NM_001291303.3(FAT4):c.2021G>A (p.Arg674His)
|
rs759309740
|
0.00004
|
NM_001291303.3(FAT4):c.2265A>C (p.Glu755Asp)
|
rs377230037
|
0.00004
|
NM_001291303.3(FAT4):c.2343C>T (p.Ile781=)
|
rs373586010
|
0.00004
|
NM_001291303.3(FAT4):c.2620A>G (p.Thr874Ala)
|
rs200064090
|
0.00004
|
NM_001291303.3(FAT4):c.2689A>G (p.Ile897Val)
|
rs112101185
|
0.00004
|
NM_001291303.3(FAT4):c.283A>T (p.Thr95Ser)
|
rs202107203
|
0.00004
|
NM_001291303.3(FAT4):c.3041G>A (p.Arg1014Gln)
|
rs377288957
|
0.00004
|
NM_001291303.3(FAT4):c.3095C>T (p.Ala1032Val)
|
rs754931963
|
0.00004
|
NM_001291303.3(FAT4):c.3351G>A (p.Ser1117=)
|
rs769768427
|
0.00004
|
NM_001291303.3(FAT4):c.3466A>G (p.Thr1156Ala)
|
rs372642535
|
0.00004
|
NM_001291303.3(FAT4):c.4081G>A (p.Gly1361Arg)
|
rs200361960
|
0.00004
|
NM_001291303.3(FAT4):c.4228G>A (p.Val1410Met)
|
rs781736766
|
0.00004
|
NM_001291303.3(FAT4):c.446G>A (p.Ser149Asn)
|
rs1003177796
|
0.00004
|
NM_001291303.3(FAT4):c.4525C>T (p.Arg1509Trp)
|
rs200214434
|
0.00004
|
NM_001291303.3(FAT4):c.4773G>A (p.Val1591=)
|
rs779545626
|
0.00004
|
NM_001291303.3(FAT4):c.4854C>T (p.Thr1618=)
|
rs764436973
|
0.00004
|
NM_001291303.3(FAT4):c.5011C>T (p.Arg1671Cys)
|
rs373116363
|
0.00004
|
NM_001291303.3(FAT4):c.5012G>A (p.Arg1671His)
|
rs375605783
|
0.00004
|
NM_001291303.3(FAT4):c.5034A>G (p.Gly1678=)
|
rs557542395
|
0.00004
|
NM_001291303.3(FAT4):c.548G>A (p.Gly183Glu)
|
rs771566742
|
0.00004
|
NM_001291303.3(FAT4):c.5532C>T (p.Pro1844=)
|
rs374897074
|
0.00004
|
NM_001291303.3(FAT4):c.5598G>A (p.Thr1866=)
|
rs370130221
|
0.00004
|
NM_001291303.3(FAT4):c.5943T>C (p.Tyr1981=)
|
rs149373164
|
0.00004
|
NM_001291303.3(FAT4):c.5991T>G (p.Asn1997Lys)
|
rs578105928
|
0.00004
|
NM_001291303.3(FAT4):c.5993G>A (p.Gly1998Asp)
|
rs753912480
|
0.00004
|
NM_001291303.3(FAT4):c.6086C>T (p.Ser2029Phe)
|
rs145573597
|
0.00004
|
NM_001291303.3(FAT4):c.6160C>G (p.Pro2054Ala)
|
rs892209188
|
0.00004
|
NM_001291303.3(FAT4):c.6532G>A (p.Ala2178Thr)
|
rs373678302
|
0.00004
|
NM_001291303.3(FAT4):c.6575G>A (p.Gly2192Asp)
|
rs752648220
|
0.00004
|
NM_001291303.3(FAT4):c.6672C>G (p.Thr2224=)
|
rs756001382
|
0.00004
|
NM_001291303.3(FAT4):c.7962C>T (p.Tyr2654=)
|
rs546465658
|
0.00004
|
NM_001291303.3(FAT4):c.9006G>A (p.Thr3002=)
|
rs142357260
|
0.00004
|
NM_001291303.3(FAT4):c.9119C>T (p.Thr3040Met)
|
rs778223332
|
0.00004
|
NM_001291303.3(FAT4):c.91C>T (p.Leu31=)
|
rs756659900
|
0.00004
|
NM_001291303.3(FAT4):c.9235A>G (p.Ile3079Val)
|
rs138817920
|
0.00004
|
NM_001291303.3(FAT4):c.9273C>A (p.Phe3091Leu)
|
rs748266278
|
0.00004
|
NM_001291303.3(FAT4):c.9290G>A (p.Ser3097Asn)
|
rs766108453
|
0.00004
|
NM_001291303.3(FAT4):c.9695C>T (p.Ala3232Val)
|
rs373873722
|
0.00004
|
NM_001291303.3(FAT4):c.9896G>A (p.Arg3299His)
|
rs370611770
|
0.00004
|
NM_001291303.3(FAT4):c.9946G>T (p.Gly3316Cys)
|
rs776046433
|
0.00004
|
NM_001291303.3(FAT4):c.1017G>T (p.Ala339=)
|
rs370554535
|
0.00003
|
NM_001291303.3(FAT4):c.10218T>C (p.Phe3406=)
|
rs986973949
|
0.00003
|
NM_001291303.3(FAT4):c.10689C>T (p.Ser3563=)
|
rs200550116
|
0.00003
|
NM_001291303.3(FAT4):c.10940A>G (p.Asp3647Gly)
|
rs780015426
|
0.00003
|
NM_001291303.3(FAT4):c.11039C>T (p.Thr3680Met)
|
rs367877267
|
0.00003
|
NM_001291303.3(FAT4):c.12406A>G (p.Ile4136Val)
|
rs149985937
|
0.00003
|
NM_001291303.3(FAT4):c.12604+16C>T
|
rs544354334
|
0.00003
|
NM_001291303.3(FAT4):c.14139G>A (p.Thr4713=)
|
rs1336245600
|
0.00003
|
NM_001291303.3(FAT4):c.14430A>G (p.Ala4810=)
|
rs144297905
|
0.00003
|
NM_001291303.3(FAT4):c.14476T>C (p.Ser4826Pro)
|
rs374891029
|
0.00003
|
NM_001291303.3(FAT4):c.14486G>C (p.Arg4829Thr)
|
rs368984725
|
0.00003
|
NM_001291303.3(FAT4):c.1663C>T (p.Arg555Trp)
|
rs756991867
|
0.00003
|
NM_001291303.3(FAT4):c.1846G>A (p.Gly616Arg)
|
rs775818322
|
0.00003
|
NM_001291303.3(FAT4):c.2014A>G (p.Met672Val)
|
rs772308456
|
0.00003
|
NM_001291303.3(FAT4):c.2225G>A (p.Ser742Asn)
|
rs201172737
|
0.00003
|
NM_001291303.3(FAT4):c.247A>G (p.Ile83Val)
|
rs375241448
|
0.00003
|
NM_001291303.3(FAT4):c.3059C>T (p.Ala1020Val)
|
rs967633574
|
0.00003
|
NM_001291303.3(FAT4):c.3328G>A (p.Glu1110Lys)
|
rs377275274
|
0.00003
|
NM_001291303.3(FAT4):c.3488G>A (p.Arg1163Lys)
|
rs375552506
|
0.00003
|
NM_001291303.3(FAT4):c.3978A>G (p.Glu1326=)
|
rs201916729
|
0.00003
|
NM_001291303.3(FAT4):c.4198C>T (p.Arg1400Cys)
|
rs764898249
|
0.00003
|
NM_001291303.3(FAT4):c.4542C>T (p.Asn1514=)
|
rs199793434
|
0.00003
|
NM_001291303.3(FAT4):c.458A>G (p.Gln153Arg)
|
rs745934649
|
0.00003
|
NM_001291303.3(FAT4):c.4736G>A (p.Arg1579His)
|
rs753125479
|
0.00003
|
NM_001291303.3(FAT4):c.5229C>T (p.Asp1743=)
|
rs777915862
|
0.00003
|
NM_001291303.3(FAT4):c.5468C>T (p.Ser1823Leu)
|
rs758045956
|
0.00003
|
NM_001291303.3(FAT4):c.5808T>C (p.Asp1936=)
|
rs770131334
|
0.00003
|
NM_001291303.3(FAT4):c.5939C>T (p.Thr1980Ile)
|
rs1458249935
|
0.00003
|
NM_001291303.3(FAT4):c.6210C>T (p.Phe2070=)
|
rs771989829
|
0.00003
|
NM_001291303.3(FAT4):c.6583A>G (p.Asn2195Asp)
|
rs1345737224
|
0.00003
|
NM_001291303.3(FAT4):c.733G>A (p.Asp245Asn)
|
rs563002306
|
0.00003
|
NM_001291303.3(FAT4):c.9486C>T (p.His3162=)
|
rs752419214
|
0.00003
|
NM_001291303.3(FAT4):c.9494C>T (p.Thr3165Met)
|
rs770333760
|
0.00003
|
NM_001291303.3(FAT4):c.10031G>A (p.Arg3344Gln)
|
rs769028469
|
0.00002
|
NM_001291303.3(FAT4):c.10227C>T (p.Asn3409=)
|
rs368992969
|
0.00002
|
NM_001291303.3(FAT4):c.10311C>T (p.Pro3437=)
|
rs762632698
|
0.00002
|
NM_001291303.3(FAT4):c.10339G>A (p.Gly3447Arg)
|
rs751776479
|
0.00002
|
NM_001291303.3(FAT4):c.10357G>A (p.Gly3453Ser)
|
rs369887674
|
0.00002
|
NM_001291303.3(FAT4):c.10748A>C (p.Tyr3583Ser)
|
rs761927639
|
0.00002
|
NM_001291303.3(FAT4):c.11053G>A (p.Val3685Ile)
|
rs761409589
|
0.00002
|
NM_001291303.3(FAT4):c.11152C>T (p.Arg3718Cys)
|
rs774217003
|
0.00002
|
NM_001291303.3(FAT4):c.11191C>G (p.His3731Asp)
|
rs1389488510
|
0.00002
|
NM_001291303.3(FAT4):c.11286G>A (p.Thr3762=)
|
rs1304302008
|
0.00002
|
NM_001291303.3(FAT4):c.1163C>T (p.Pro388Leu)
|
rs991371776
|
0.00002
|
NM_001291303.3(FAT4):c.11814A>C (p.Glu3938Asp)
|
rs763572933
|
0.00002
|
NM_001291303.3(FAT4):c.11920C>T (p.His3974Tyr)
|
rs776196417
|
0.00002
|
NM_001291303.3(FAT4):c.12023A>T (p.Lys4008Ile)
|
rs138368884
|
0.00002
|
NM_001291303.3(FAT4):c.12115T>G (p.Phe4039Val)
|
rs775446398
|
0.00002
|
NM_001291303.3(FAT4):c.12823-12T>C
|
rs370388016
|
0.00002
|
NM_001291303.3(FAT4):c.13144G>A (p.Gly4382Arg)
|
rs368409720
|
0.00002
|
NM_001291303.3(FAT4):c.13180C>T (p.Pro4394Ser)
|
rs772779154
|
0.00002
|
NM_001291303.3(FAT4):c.13209G>A (p.Pro4403=)
|
rs763983959
|
0.00002
|
NM_001291303.3(FAT4):c.13478T>C (p.Leu4493Pro)
|
rs773146282
|
0.00002
|
NM_001291303.3(FAT4):c.13549G>T (p.Val4517Phe)
|
rs142649500
|
0.00002
|
NM_001291303.3(FAT4):c.13594A>G (p.Arg4532Gly)
|
rs373502916
|
0.00002
|
NM_001291303.3(FAT4):c.13601A>G (p.Lys4534Arg)
|
rs749145679
|
0.00002
|
NM_001291303.3(FAT4):c.13851G>A (p.Gln4617=)
|
rs753469438
|
0.00002
|
NM_001291303.3(FAT4):c.13965G>A (p.Arg4655=)
|
rs756243213
|
0.00002
|
NM_001291303.3(FAT4):c.14169G>T (p.Leu4723Phe)
|
rs760377475
|
0.00002
|
NM_001291303.3(FAT4):c.14179A>G (p.Ile4727Val)
|
rs764430401
|
0.00002
|
NM_001291303.3(FAT4):c.14495C>T (p.Ala4832Val)
|
rs759650967
|
0.00002
|
NM_001291303.3(FAT4):c.14680A>G (p.Arg4894Gly)
|
rs780871857
|
0.00002
|
NM_001291303.3(FAT4):c.14738G>A (p.Gly4913Asp)
|
rs765666547
|
0.00002
|
NM_001291303.3(FAT4):c.1608C>T (p.Ser536=)
|
rs375970737
|
0.00002
|
NM_001291303.3(FAT4):c.1845C>T (p.Asn615=)
|
rs548524386
|
0.00002
|
NM_001291303.3(FAT4):c.2158A>G (p.Thr720Ala)
|
rs367762836
|
0.00002
|
NM_001291303.3(FAT4):c.2287A>G (p.Ile763Val)
|
rs774554680
|
0.00002
|
NM_001291303.3(FAT4):c.2376A>G (p.Val792=)
|
rs779400775
|
0.00002
|
NM_001291303.3(FAT4):c.2382T>G (p.Ser794Arg)
|
rs746206634
|
0.00002
|
NM_001291303.3(FAT4):c.2412G>A (p.Glu804=)
|
rs776202236
|
0.00002
|
NM_001291303.3(FAT4):c.2646A>T (p.Thr882=)
|
rs187912140
|
0.00002
|
NM_001291303.3(FAT4):c.3153A>G (p.Gln1051=)
|
rs372689449
|
0.00002
|
NM_001291303.3(FAT4):c.3350C>T (p.Ser1117Leu)
|
rs1228464959
|
0.00002
|
NM_001291303.3(FAT4):c.3736C>T (p.His1246Tyr)
|
rs770886307
|
0.00002
|
NM_001291303.3(FAT4):c.3836C>T (p.Pro1279Leu)
|
rs1299025550
|
0.00002
|
NM_001291303.3(FAT4):c.3960C>T (p.Leu1320=)
|
rs745691036
|
0.00002
|
NM_001291303.3(FAT4):c.4032A>G (p.Ser1344=)
|
rs201020367
|
0.00002
|
NM_001291303.3(FAT4):c.4060A>G (p.Ile1354Val)
|
rs200273982
|
0.00002
|
NM_001291303.3(FAT4):c.4274T>G (p.Ile1425Ser)
|
rs759931847
|
0.00002
|
NM_001291303.3(FAT4):c.4394G>A (p.Arg1465Lys)
|
rs776002583
|
0.00002
|
NM_001291303.3(FAT4):c.4417G>A (p.Glu1473Lys)
|
rs377534767
|
0.00002
|
NM_001291303.3(FAT4):c.4471C>T (p.Leu1491Phe)
|
rs374317713
|
0.00002
|
NM_001291303.3(FAT4):c.4636G>A (p.Val1546Ile)
|
rs755526114
|
0.00002
|
NM_001291303.3(FAT4):c.469G>T (p.Asp157Tyr)
|
rs759072210
|
0.00002
|
NM_001291303.3(FAT4):c.4964G>A (p.Ser1655Asn)
|
rs572010193
|
0.00002
|
NM_001291303.3(FAT4):c.4992G>A (p.Glu1664=)
|
rs751217207
|
0.00002
|
NM_001291303.3(FAT4):c.5035C>T (p.Arg1679Cys)
|
rs569440986
|
0.00002
|
NM_001291303.3(FAT4):c.5057A>G (p.His1686Arg)
|
rs555458566
|
0.00002
|
NM_001291303.3(FAT4):c.5191C>G (p.Gln1731Glu)
|
rs367948625
|
0.00002
|
NM_001291303.3(FAT4):c.5284C>G (p.Leu1762Val)
|
rs372610330
|
0.00002
|
NM_001291303.3(FAT4):c.5308-10C>T
|
rs543998358
|
0.00002
|
NM_001291303.3(FAT4):c.5379C>T (p.Ser1793=)
|
rs202160050
|
0.00002
|
NM_001291303.3(FAT4):c.5380G>A (p.Gly1794Arg)
|
rs200789529
|
0.00002
|
NM_001291303.3(FAT4):c.5444G>A (p.Arg1815His)
|
rs774484692
|
0.00002
|
NM_001291303.3(FAT4):c.5490T>G (p.Thr1830=)
|
rs1262944393
|
0.00002
|
NM_001291303.3(FAT4):c.5645A>G (p.Glu1882Gly)
|
rs757125413
|
0.00002
|
NM_001291303.3(FAT4):c.60A>G (p.Ser20=)
|
rs369059252
|
0.00002
|
NM_001291303.3(FAT4):c.6444T>C (p.Asn2148=)
|
rs779420772
|
0.00002
|
NM_001291303.3(FAT4):c.6531C>T (p.Phe2177=)
|
rs775866114
|
0.00002
|
NM_001291303.3(FAT4):c.6577A>C (p.Ile2193Leu)
|
rs755984729
|
0.00002
|
NM_001291303.3(FAT4):c.7024C>T (p.Pro2342Ser)
|
rs769744109
|
0.00002
|
NM_001291303.3(FAT4):c.7743C>T (p.Asn2581=)
|
rs747133003
|
0.00002
|
NM_001291303.3(FAT4):c.7966A>C (p.Lys2656Gln)
|
rs760398912
|
0.00002
|
NM_001291303.3(FAT4):c.8205G>A (p.Arg2735=)
|
rs769526903
|
0.00002
|
NM_001291303.3(FAT4):c.8214A>G (p.Val2738=)
|
rs772966185
|
0.00002
|
NM_001291303.3(FAT4):c.8818G>A (p.Val2940Ile)
|
rs746085629
|
0.00002
|
NM_001291303.3(FAT4):c.8861T>G (p.Ile2954Arg)
|
rs762222146
|
0.00002
|
NM_001291303.3(FAT4):c.8879G>A (p.Arg2960Gln)
|
rs961185884
|
0.00002
|
NM_001291303.3(FAT4):c.9087C>T (p.Asn3029=)
|
rs201663831
|
0.00002
|
NM_001291303.3(FAT4):c.9095G>C (p.Gly3032Ala)
|
rs758240945
|
0.00002
|
NM_001291303.3(FAT4):c.9113A>G (p.Asn3038Ser)
|
rs748679291
|
0.00002
|
NM_001291303.3(FAT4):c.9156C>A (p.Asp3052Glu)
|
rs761372826
|
0.00002
|
NM_001291303.3(FAT4):c.9208C>T (p.Pro3070Ser)
|
rs998399883
|
0.00002
|
NM_001291303.3(FAT4):c.9441A>G (p.Ile3147Met)
|
rs375872898
|
0.00002
|
NM_001291303.3(FAT4):c.9696G>A (p.Ala3232=)
|
rs142877205
|
0.00002
|
NM_001291303.3(FAT4):c.9800A>G (p.His3267Arg)
|
rs773545119
|
0.00002
|
NM_001291303.3(FAT4):c.10024A>C (p.Asn3342His)
|
rs772182074
|
0.00001
|
NM_001291303.3(FAT4):c.10060A>G (p.Thr3354Ala)
|
rs759036002
|
0.00001
|
NM_001291303.3(FAT4):c.10095A>G (p.Arg3365=)
|
rs1240262001
|
0.00001
|
NM_001291303.3(FAT4):c.1012G>A (p.Glu338Lys)
|
rs1452017220
|
0.00001
|
NM_001291303.3(FAT4):c.10155T>C (p.Gly3385=)
|
rs780130895
|
0.00001
|
NM_001291303.3(FAT4):c.10189G>A (p.Val3397Met)
|
rs531437241
|
0.00001
|
NM_001291303.3(FAT4):c.10262T>C (p.Ile3421Thr)
|
rs1726059124
|
0.00001
|
NM_001291303.3(FAT4):c.10290C>T (p.Ala3430=)
|
rs746579341
|
0.00001
|
NM_001291303.3(FAT4):c.10395C>T (p.Thr3465=)
|
rs768300702
|
0.00001
|
NM_001291303.3(FAT4):c.10527G>A (p.Gly3509=)
|
rs757649049
|
0.00001
|
NM_001291303.3(FAT4):c.10644T>C (p.Tyr3548=)
|
rs750863500
|
0.00001
|
NM_001291303.3(FAT4):c.10690A>G (p.Thr3564Ala)
|
rs778801952
|
0.00001
|
NM_001291303.3(FAT4):c.10756G>T (p.Val3586Leu)
|
rs1726084759
|
0.00001
|
NM_001291303.3(FAT4):c.10793C>G (p.Ser3598Cys)
|
rs558897707
|
0.00001
|
NM_001291303.3(FAT4):c.10868T>C (p.Val3623Ala)
|
rs530781443
|
0.00001
|
NM_001291303.3(FAT4):c.10882A>C (p.Asn3628His)
|
rs374041907
|
0.00001
|
NM_001291303.3(FAT4):c.10G>A (p.Ala4Thr)
|
rs942468629
|
0.00001
|
NM_001291303.3(FAT4):c.11034T>C (p.Asp3678=)
|
rs553335263
|
0.00001
|
NM_001291303.3(FAT4):c.11080A>G (p.Thr3694Ala)
|
rs150752497
|
0.00001
|
NM_001291303.3(FAT4):c.11121C>T (p.Ser3707=)
|
rs747348231
|
0.00001
|
NM_001291303.3(FAT4):c.11134G>T (p.Asp3712Tyr)
|
rs769490380
|
0.00001
|
NM_001291303.3(FAT4):c.11205T>G (p.Phe3735Leu)
|
rs1319618330
|
0.00001
|
NM_001291303.3(FAT4):c.11256G>A (p.Leu3752=)
|
rs372230232
|
0.00001
|
NM_001291303.3(FAT4):c.11277C>A (p.Asn3759Lys)
|
rs1726115578
|
0.00001
|
NM_001291303.3(FAT4):c.11321A>G (p.Gln3774Arg)
|
rs1387872729
|
0.00001
|
NM_001291303.3(FAT4):c.11341G>A (p.Val3781Ile)
|
rs764537596
|
0.00001
|
NM_001291303.3(FAT4):c.11373C>A (p.Ile3791=)
|
rs1017830368
|
0.00001
|
NM_001291303.3(FAT4):c.1137G>A (p.Leu379=)
|
rs763558049
|
0.00001
|
NM_001291303.3(FAT4):c.11482G>A (p.Val3828Ile)
|
rs773534151
|
0.00001
|
NM_001291303.3(FAT4):c.11556T>C (p.Cys3852=)
|
rs772913685
|
0.00001
|
NM_001291303.3(FAT4):c.11560C>G (p.Pro3854Ala)
|
rs1165023117
|
0.00001
|
NM_001291303.3(FAT4):c.11570C>T (p.Ala3857Val)
|
rs536513777
|
0.00001
|
NM_001291303.3(FAT4):c.11694G>A (p.Ala3898=)
|
rs189735159
|
0.00001
|
NM_001291303.3(FAT4):c.11706T>A (p.Asp3902Glu)
|
rs774612831
|
0.00001
|
NM_001291303.3(FAT4):c.11841C>A (p.Asn3947Lys)
|
rs758141491
|
0.00001
|
NM_001291303.3(FAT4):c.11872G>A (p.Gly3958Ser)
|
rs557600491
|
0.00001
|
NM_001291303.3(FAT4):c.11905+10A>T
|
rs748192134
|
0.00001
|
NM_001291303.3(FAT4):c.11912T>G (p.Phe3971Cys)
|
rs746181472
|
0.00001
|
NM_001291303.3(FAT4):c.11928G>A (p.Glu3976=)
|
rs773066963
|
0.00001
|
NM_001291303.3(FAT4):c.12100G>A (p.Glu4034Lys)
|
rs1277850395
|
0.00001
|
NM_001291303.3(FAT4):c.12107G>C (p.Arg4036Thr)
|
rs897405265
|
0.00001
|
NM_001291303.3(FAT4):c.12144T>C (p.Tyr4048=)
|
rs1475901716
|
0.00001
|
NM_001291303.3(FAT4):c.12147G>A (p.Lys4049=)
|
rs1199506652
|
0.00001
|
NM_001291303.3(FAT4):c.12150C>T (p.Leu4050=)
|
rs1434766338
|
0.00001
|
NM_001291303.3(FAT4):c.12213+13A>G
|
rs1239636831
|
0.00001
|
NM_001291303.3(FAT4):c.12274A>G (p.Ser4092Gly)
|
rs1326543871
|
0.00001
|
NM_001291303.3(FAT4):c.12286G>A (p.Val4096Ile)
|
rs768534192
|
0.00001
|
NM_001291303.3(FAT4):c.12300-10A>G
|
rs779397693
|
0.00001
|
NM_001291303.3(FAT4):c.12340A>G (p.Ile4114Val)
|
rs948622582
|
0.00001
|
NM_001291303.3(FAT4):c.12356C>G (p.Pro4119Arg)
|
rs1403495139
|
0.00001
|
NM_001291303.3(FAT4):c.1237A>G (p.Lys413Glu)
|
rs1471306819
|
0.00001
|
NM_001291303.3(FAT4):c.12414G>T (p.Glu4138Asp)
|
rs754509390
|
0.00001
|
NM_001291303.3(FAT4):c.12465A>G (p.Gln4155=)
|
rs1727063661
|
0.00001
|
NM_001291303.3(FAT4):c.12479+7C>T
|
rs769242691
|
0.00001
|
NM_001291303.3(FAT4):c.12480-18C>T
|
rs774996883
|
0.00001
|
NM_001291303.3(FAT4):c.12546C>T (p.Tyr4182=)
|
rs781777881
|
0.00001
|
NM_001291303.3(FAT4):c.12604+15C>A
|
rs1472760762
|
0.00001
|
NM_001291303.3(FAT4):c.12611C>T (p.Thr4204Ile)
|
rs1173461199
|
0.00001
|
NM_001291303.3(FAT4):c.12680G>A (p.Arg4227Gln)
|
rs759859751
|
0.00001
|
NM_001291303.3(FAT4):c.1273G>C (p.Ala425Pro)
|
rs138548779
|
0.00001
|
NM_001291303.3(FAT4):c.12745G>A (p.Glu4249Lys)
|
rs779280729
|
0.00001
|
NM_001291303.3(FAT4):c.1276T>A (p.Leu426Met)
|
rs1235926992
|
0.00001
|
NM_001291303.3(FAT4):c.12792C>T (p.Ile4264=)
|
rs1030247873
|
0.00001
|
NM_001291303.3(FAT4):c.12822+7T>C
|
rs372948727
|
0.00001
|
NM_001291303.3(FAT4):c.12842A>C (p.Tyr4281Ser)
|
rs758804032
|
0.00001
|
NM_001291303.3(FAT4):c.12861A>C (p.Gly4287=)
|
rs756816700
|
0.00001
|
NM_001291303.3(FAT4):c.129C>G (p.Ala43=)
|
rs769721255
|
0.00001
|
NM_001291303.3(FAT4):c.13011C>T (p.Phe4337=)
|
rs778396214
|
0.00001
|
NM_001291303.3(FAT4):c.13194T>C (p.Ile4398=)
|
rs1727557813
|
0.00001
|
NM_001291303.3(FAT4):c.13260G>A (p.Gln4420=)
|
rs770683738
|
0.00001
|
NM_001291303.3(FAT4):c.13275G>A (p.Arg4425=)
|
rs759100088
|
0.00001
|
NM_001291303.3(FAT4):c.132G>C (p.Glu44Asp)
|
rs763601689
|
0.00001
|
NM_001291303.3(FAT4):c.13305C>A (p.His4435Gln)
|
rs1357034003
|
0.00001
|
NM_001291303.3(FAT4):c.13367C>T (p.Pro4456Leu)
|
rs770036596
|
0.00001
|
NM_001291303.3(FAT4):c.13416C>T (p.Gly4472=)
|
rs141983394
|
0.00001
|
NM_001291303.3(FAT4):c.13461G>C (p.Ala4487=)
|
rs776669972
|
0.00001
|
NM_001291303.3(FAT4):c.13530C>T (p.Ile4510=)
|
rs774693839
|
0.00001
|
NM_001291303.3(FAT4):c.13564G>C (p.Val4522Leu)
|
rs200205392
|
0.00001
|
NM_001291303.3(FAT4):c.13621G>A (p.Glu4541Lys)
|
rs775440091
|
0.00001
|
NM_001291303.3(FAT4):c.13700A>G (p.Tyr4567Cys)
|
rs772246636
|
0.00001
|
NM_001291303.3(FAT4):c.13807A>G (p.Asn4603Asp)
|
rs780176625
|
0.00001
|
NM_001291303.3(FAT4):c.13941C>T (p.His4647=)
|
rs1195396838
|
0.00001
|
NM_001291303.3(FAT4):c.14105G>A (p.Arg4702Gln)
|
rs765222973
|
0.00001
|
NM_001291303.3(FAT4):c.14186A>T (p.Asp4729Val)
|
rs372142864
|
0.00001
|
NM_001291303.3(FAT4):c.141G>A (p.Gln47=)
|
rs1456423170
|
0.00001
|
NM_001291303.3(FAT4):c.14205G>A (p.Met4735Ile)
|
rs566319855
|
0.00001
|
NM_001291303.3(FAT4):c.14273C>T (p.Pro4758Leu)
|
rs1405492776
|
0.00001
|
NM_001291303.3(FAT4):c.14304A>G (p.Pro4768=)
|
rs1217156870
|
0.00001
|
NM_001291303.3(FAT4):c.14376A>C (p.Glu4792Asp)
|
rs200724983
|
0.00001
|
NM_001291303.3(FAT4):c.14401C>T (p.Arg4801Cys)
|
rs199895179
|
0.00001
|
NM_001291303.3(FAT4):c.14402G>A (p.Arg4801His)
|
rs766392638
|
0.00001
|
NM_001291303.3(FAT4):c.14433C>G (p.Asp4811Glu)
|
rs368166167
|
0.00001
|
NM_001291303.3(FAT4):c.14441G>A (p.Arg4814Lys)
|
rs756452113
|
0.00001
|
NM_001291303.3(FAT4):c.14471C>T (p.Pro4824Leu)
|
rs781260706
|
0.00001
|
NM_001291303.3(FAT4):c.144G>A (p.Val48=)
|
rs1396893351
|
0.00001
|
NM_001291303.3(FAT4):c.14670G>A (p.Leu4890=)
|
rs1393875507
|
0.00001
|
NM_001291303.3(FAT4):c.14701G>A (p.Glu4901Lys)
|
rs746119916
|
0.00001
|
NM_001291303.3(FAT4):c.14818C>T (p.Pro4940Ser)
|
rs1727651107
|
0.00001
|
NM_001291303.3(FAT4):c.14836G>T (p.Val4946Leu)
|
rs1025769012
|
0.00001
|
NM_001291303.3(FAT4):c.1485T>C (p.Ser495=)
|
rs370574664
|
0.00001
|
NM_001291303.3(FAT4):c.1537A>G (p.Ser513Gly)
|
rs750439197
|
0.00001
|
NM_001291303.3(FAT4):c.1613G>A (p.Gly538Glu)
|
rs1193758539
|
0.00001
|
NM_001291303.3(FAT4):c.1642A>G (p.Ile548Val)
|
rs1373319772
|
0.00001
|
NM_001291303.3(FAT4):c.173G>T (p.Gly58Val)
|
rs749929736
|
0.00001
|
NM_001291303.3(FAT4):c.176C>T (p.Thr59Ile)
|
rs757284999
|
0.00001
|
NM_001291303.3(FAT4):c.1824T>C (p.Thr608=)
|
rs1261675128
|
0.00001
|
NM_001291303.3(FAT4):c.1882G>A (p.Asp628Asn)
|
rs1730736994
|
0.00001
|
NM_001291303.3(FAT4):c.1956A>G (p.Gln652=)
|
rs761128725
|
0.00001
|
NM_001291303.3(FAT4):c.1980G>A (p.Leu660=)
|
rs1355988118
|
0.00001
|
NM_001291303.3(FAT4):c.2004C>A (p.Pro668=)
|
rs757005620
|
0.00001
|
NM_001291303.3(FAT4):c.2057G>A (p.Ser686Asn)
|
rs374104309
|
0.00001
|
NM_001291303.3(FAT4):c.2085T>C (p.Phe695=)
|
rs778718253
|
0.00001
|
NM_001291303.3(FAT4):c.2145C>T (p.Asp715=)
|
rs748717152
|
0.00001
|
NM_001291303.3(FAT4):c.217A>G (p.Arg73Gly)
|
rs771620229
|
0.00001
|
NM_001291303.3(FAT4):c.2204G>A (p.Arg735Gln)
|
rs376468352
|
0.00001
|
NM_001291303.3(FAT4):c.2324A>G (p.Asn775Ser)
|
rs762681862
|
0.00001
|
NM_001291303.3(FAT4):c.2450C>T (p.Ala817Val)
|
rs539442232
|
0.00001
|
NM_001291303.3(FAT4):c.2505G>A (p.Gln835=)
|
rs1007046760
|
0.00001
|
NM_001291303.3(FAT4):c.2641A>G (p.Ile881Val)
|
rs183643556
|
0.00001
|
NM_001291303.3(FAT4):c.2815C>T (p.Leu939=)
|
rs1479723271
|
0.00001
|
NM_001291303.3(FAT4):c.2824A>G (p.Ile942Val)
|
rs368138514
|
0.00001
|
NM_001291303.3(FAT4):c.2834A>G (p.Lys945Arg)
|
rs1376872414
|
0.00001
|
NM_001291303.3(FAT4):c.2858G>T (p.Gly953Val)
|
rs371993123
|
0.00001
|
NM_001291303.3(FAT4):c.286A>G (p.Ile96Val)
|
rs778038668
|
0.00001
|
NM_001291303.3(FAT4):c.2886C>T (p.Tyr962=)
|
rs1302137252
|
0.00001
|
NM_001291303.3(FAT4):c.2896A>G (p.Ile966Val)
|
rs778631726
|
0.00001
|
NM_001291303.3(FAT4):c.3003T>C (p.Tyr1001=)
|
rs1295148063
|
0.00001
|
NM_001291303.3(FAT4):c.321C>A (p.Asn107Lys)
|
rs772612640
|
0.00001
|
NM_001291303.3(FAT4):c.3236C>T (p.Pro1079Leu)
|
rs185325824
|
0.00001
|
NM_001291303.3(FAT4):c.327G>A (p.Val109=)
|
rs1248289171
|
0.00001
|
NM_001291303.3(FAT4):c.3315C>T (p.Tyr1105=)
|
rs374329069
|
0.00001
|
NM_001291303.3(FAT4):c.3470A>C (p.Asn1157Thr)
|
rs764042588
|
0.00001
|
NM_001291303.3(FAT4):c.3479A>G (p.Gln1160Arg)
|
rs776512346
|
0.00001
|
NM_001291303.3(FAT4):c.3532A>G (p.Thr1178Ala)
|
rs1043570092
|
0.00001
|
NM_001291303.3(FAT4):c.3637G>T (p.Asp1213Tyr)
|
rs762595829
|
0.00001
|
NM_001291303.3(FAT4):c.3722A>G (p.Asn1241Ser)
|
rs200169047
|
0.00001
|
NM_001291303.3(FAT4):c.3879C>T (p.Ile1293=)
|
rs559084790
|
0.00001
|
NM_001291303.3(FAT4):c.3896G>A (p.Cys1299Tyr)
|
rs374884564
|
0.00001
|
NM_001291303.3(FAT4):c.4257C>G (p.Ser1419Arg)
|
rs377613970
|
0.00001
|
NM_001291303.3(FAT4):c.4273A>G (p.Ile1425Val)
|
rs774883256
|
0.00001
|
NM_001291303.3(FAT4):c.4318A>G (p.Ile1440Val)
|
rs376480835
|
0.00001
|
NM_001291303.3(FAT4):c.4365A>G (p.Leu1455=)
|
rs757401187
|
0.00001
|
NM_001291303.3(FAT4):c.4368C>A (p.Ser1456=)
|
rs997026775
|
0.00001
|
NM_001291303.3(FAT4):c.4382A>G (p.Gln1461Arg)
|
rs1468654357
|
0.00001
|
NM_001291303.3(FAT4):c.44C>G (p.Pro15Arg)
|
rs375956663
|
0.00001
|
NM_001291303.3(FAT4):c.4502A>C (p.Gln1501Pro)
|
rs1730912386
|
0.00001
|
NM_001291303.3(FAT4):c.4526G>A (p.Arg1509Gln)
|
rs776836295
|
0.00001
|
NM_001291303.3(FAT4):c.4563C>T (p.Asp1521=)
|
rs201637012
|
0.00001
|
NM_001291303.3(FAT4):c.4584G>A (p.Met1528Ile)
|
rs1417100834
|
0.00001
|
NM_001291303.3(FAT4):c.4701C>T (p.Ile1567=)
|
rs898704198
|
0.00001
|
NM_001291303.3(FAT4):c.473C>G (p.Thr158Ser)
|
rs767365327
|
0.00001
|
NM_001291303.3(FAT4):c.4815C>T (p.Asp1605=)
|
rs763330003
|
0.00001
|
NM_001291303.3(FAT4):c.4821G>T (p.Gly1607=)
|
rs759482090
|
0.00001
|
NM_001291303.3(FAT4):c.4903A>G (p.Ile1635Val)
|
rs754135078
|
0.00001
|
NM_001291303.3(FAT4):c.4962T>C (p.Ala1654=)
|
rs547299465
|
0.00001
|
NM_001291303.3(FAT4):c.5030T>C (p.Val1677Ala)
|
rs371042493
|
0.00001
|
NM_001291303.3(FAT4):c.5093G>A (p.Arg1698Gln)
|
rs777384285
|
0.00001
|
NM_001291303.3(FAT4):c.5122G>T (p.Asp1708Tyr)
|
rs778860447
|
0.00001
|
NM_001291303.3(FAT4):c.5268C>T (p.Gly1756=)
|
rs747899632
|
0.00001
|
NM_001291303.3(FAT4):c.5308-19G>A
|
rs1369164587
|
0.00001
|
NM_001291303.3(FAT4):c.5308-8T>A
|
rs1734632611
|
0.00001
|
NM_001291303.3(FAT4):c.5308-9T>C
|
rs199866344
|
0.00001
|
NM_001291303.3(FAT4):c.5345G>A (p.Gly1782Glu)
|
rs1734635696
|
0.00001
|
NM_001291303.3(FAT4):c.5354A>G (p.Asp1785Gly)
|
rs150299411
|
0.00001
|
NM_001291303.3(FAT4):c.535G>A (p.Gly179Ser)
|
rs748505773
|
0.00001
|
NM_001291303.3(FAT4):c.5362C>T (p.Arg1788Cys)
|
rs768397789
|
0.00001
|
NM_001291303.3(FAT4):c.5392G>A (p.Ala1798Thr)
|
rs1465250521
|
0.00001
|
NM_001291303.3(FAT4):c.5423C>G (p.Ser1808Cys)
|
rs570452440
|
0.00001
|
NM_001291303.3(FAT4):c.5424C>G (p.Ser1808=)
|
rs200354953
|
0.00001
|
NM_001291303.3(FAT4):c.5441T>C (p.Val1814Ala)
|
rs370491665
|
0.00001
|
NM_001291303.3(FAT4):c.5501T>G (p.Val1834Gly)
|
rs748063320
|
0.00001
|
NM_001291303.3(FAT4):c.550C>G (p.Arg184Gly)
|
rs775309368
|
0.00001
|
NM_001291303.3(FAT4):c.5584G>A (p.Ala1862Thr)
|
rs777004693
|
0.00001
|
NM_001291303.3(FAT4):c.5623G>C (p.Glu1875Gln)
|
rs1189699181
|
0.00001
|
NM_001291303.3(FAT4):c.5692T>C (p.Phe1898Leu)
|
rs374142929
|
0.00001
|
NM_001291303.3(FAT4):c.5705G>A (p.Arg1902Gln)
|
rs367572465
|
0.00001
|
NM_001291303.3(FAT4):c.5751A>C (p.Arg1917=)
|
rs763677301
|
0.00001
|
NM_001291303.3(FAT4):c.5765G>A (p.Gly1922Glu)
|
rs1471557300
|
0.00001
|
NM_001291303.3(FAT4):c.578C>T (p.Pro193Leu)
|
rs1352317490
|
0.00001
|
NM_001291303.3(FAT4):c.5846A>G (p.Tyr1949Cys)
|
rs760392965
|
0.00001
|
NM_001291303.3(FAT4):c.5860A>G (p.Met1954Val)
|
rs758232234
|
0.00001
|
NM_001291303.3(FAT4):c.5900A>G (p.Asn1967Ser)
|
rs186847381
|
0.00001
|
NM_001291303.3(FAT4):c.5924T>C (p.Ile1975Thr)
|
rs200276252
|
0.00001
|
NM_001291303.3(FAT4):c.6109G>A (p.Val2037Ile)
|
rs1192093557
|
0.00001
|
NM_001291303.3(FAT4):c.6408A>G (p.Ser2136=)
|
rs760022203
|
0.00001
|
NM_001291303.3(FAT4):c.6466C>A (p.Gln2156Lys)
|
rs911179212
|
0.00001
|
NM_001291303.3(FAT4):c.6484G>A (p.Glu2162Lys)
|
rs771100438
|
0.00001
|
NM_001291303.3(FAT4):c.651G>C (p.Gln217His)
|
rs751560462
|
0.00001
|
NM_001291303.3(FAT4):c.6584A>G (p.Asn2195Ser)
|
rs200234420
|
0.00001
|
NM_001291303.3(FAT4):c.6630C>G (p.Ala2210=)
|
rs1049419796
|
0.00001
|
NM_001291303.3(FAT4):c.6688C>A (p.Gln2230Lys)
|
rs758534993
|
0.00001
|
NM_001291303.3(FAT4):c.6701G>A (p.Arg2234Gln)
|
rs1271830683
|
0.00001
|
NM_001291303.3(FAT4):c.6796G>C (p.Val2266Leu)
|
rs1055990626
|
0.00001
|
NM_001291303.3(FAT4):c.681G>T (p.Glu227Asp)
|
rs989816448
|
0.00001
|
NM_001291303.3(FAT4):c.7018+9A>G
|
rs778593984
|
0.00001
|
NM_001291303.3(FAT4):c.7080T>C (p.Asn2360=)
|
rs552658366
|
0.00001
|
NM_001291303.3(FAT4):c.7088C>T (p.Thr2363Ile)
|
rs780014957
|
0.00001
|
NM_001291303.3(FAT4):c.7106A>G (p.Tyr2369Cys)
|
rs538280790
|
0.00001
|
NM_001291303.3(FAT4):c.7120C>T (p.Pro2374Ser)
|
rs749817883
|
0.00001
|
NM_001291303.3(FAT4):c.7200-3T>C
|
rs1178252329
|
0.00001
|
NM_001291303.3(FAT4):c.7260C>T (p.Ile2420=)
|
rs754063392
|
0.00001
|
NM_001291303.3(FAT4):c.7335A>C (p.Pro2445=)
|
rs1475387576
|
0.00001
|
NM_001291303.3(FAT4):c.7416A>T (p.Pro2472=)
|
rs1354476033
|
0.00001
|
NM_001291303.3(FAT4):c.7516T>G (p.Ser2506Ala)
|
rs148603730
|
0.00001
|
NM_001291303.3(FAT4):c.755G>A (p.Ser252Asn)
|
rs371889798
|
0.00001
|
NM_001291303.3(FAT4):c.7578C>T (p.Ala2526=)
|
rs748125780
|
0.00001
|
NM_001291303.3(FAT4):c.7584A>C (p.Gly2528=)
|
rs777464644
|
0.00001
|
NM_001291303.3(FAT4):c.7692C>G (p.Ala2564=)
|
rs780699634
|
0.00001
|
NM_001291303.3(FAT4):c.7801A>G (p.Met2601Val)
|
rs1578655249
|
0.00001
|
NM_001291303.3(FAT4):c.780T>C (p.Pro260=)
|
rs756940330
|
0.00001
|
NM_001291303.3(FAT4):c.7876A>C (p.Ser2626Arg)
|
rs191460472
|
0.00001
|
NM_001291303.3(FAT4):c.7899G>T (p.Lys2633Asn)
|
rs763676237
|
0.00001
|
NM_001291303.3(FAT4):c.791T>A (p.Val264Asp)
|
rs746534343
|
0.00001
|
NM_001291303.3(FAT4):c.8162A>G (p.Asn2721Ser)
|
rs1452280145
|
0.00001
|
NM_001291303.3(FAT4):c.8164C>T (p.His2722Tyr)
|
rs779344742
|
0.00001
|
NM_001291303.3(FAT4):c.81G>A (p.Val27=)
|
rs560877653
|
0.00001
|
NM_001291303.3(FAT4):c.8216C>A (p.Ser2739Tyr)
|
rs748854090
|
0.00001
|
NM_001291303.3(FAT4):c.8227C>T (p.Leu2743=)
|
rs770555304
|
0.00001
|
NM_001291303.3(FAT4):c.8230A>G (p.Thr2744Ala)
|
rs774223392
|
0.00001
|
NM_001291303.3(FAT4):c.8231C>T (p.Thr2744Ile)
|
rs759455125
|
0.00001
|
NM_001291303.3(FAT4):c.8252G>T (p.Gly2751Val)
|
rs767230275
|
0.00001
|
NM_001291303.3(FAT4):c.8258C>T (p.Pro2753Leu)
|
rs1389714376
|
0.00001
|
NM_001291303.3(FAT4):c.8280A>C (p.Lys2760Asn)
|
rs750907829
|
0.00001
|
NM_001291303.3(FAT4):c.835G>A (p.Glu279Lys)
|
rs373298045
|
0.00001
|
NM_001291303.3(FAT4):c.8384G>A (p.Arg2795His)
|
rs150894990
|
0.00001
|
NM_001291303.3(FAT4):c.842C>T (p.Thr281Ile)
|
rs564305264
|
0.00001
|
NM_001291303.3(FAT4):c.8461A>G (p.Thr2821Ala)
|
rs768020749
|
0.00001
|
NM_001291303.3(FAT4):c.8520A>G (p.Thr2840=)
|
rs1201928763
|
0.00001
|
NM_001291303.3(FAT4):c.8627G>C (p.Arg2876Thr)
|
rs751105645
|
0.00001
|
NM_001291303.3(FAT4):c.8693C>T (p.Ala2898Val)
|
rs369712573
|
0.00001
|
NM_001291303.3(FAT4):c.8793T>C (p.Asn2931=)
|
rs777659155
|
0.00001
|
NM_001291303.3(FAT4):c.8849G>C (p.Arg2950Thr)
|
rs924710061
|
0.00001
|
NM_001291303.3(FAT4):c.8916C>T (p.Thr2972=)
|
rs147020561
|
0.00001
|
NM_001291303.3(FAT4):c.902A>C (p.Glu301Ala)
|
rs896894192
|
0.00001
|
NM_001291303.3(FAT4):c.9046G>A (p.Gly3016Arg)
|
rs377586866
|
0.00001
|
NM_001291303.3(FAT4):c.90A>G (p.Leu30=)
|
rs753444272
|
0.00001
|
NM_001291303.3(FAT4):c.9152C>A (p.Ser3051Tyr)
|
rs866162018
|
0.00001
|
NM_001291303.3(FAT4):c.9255C>T (p.Asn3085=)
|
rs1003467964
|
0.00001
|
NM_001291303.3(FAT4):c.9279A>C (p.Gln3093His)
|
rs769424345
|
0.00001
|
NM_001291303.3(FAT4):c.9313A>G (p.Ser3105Gly)
|
rs764097811
|
0.00001
|
NM_001291303.3(FAT4):c.9315C>G (p.Ser3105Arg)
|
rs1419658326
|
0.00001
|
NM_001291303.3(FAT4):c.9360A>G (p.Ala3120=)
|
rs957324299
|
0.00001
|
NM_001291303.3(FAT4):c.9365T>C (p.Met3122Thr)
|
rs371686578
|
0.00001
|
NM_001291303.3(FAT4):c.9410G>A (p.Gly3137Asp)
|
rs771849892
|
0.00001
|
NM_001291303.3(FAT4):c.949C>T (p.Arg317Cys)
|
rs775610806
|
0.00001
|
NM_001291303.3(FAT4):c.9511G>A (p.Gly3171Arg)
|
rs746759926
|
0.00001
|
NM_001291303.3(FAT4):c.9548C>T (p.Thr3183Ile)
|
rs571235536
|
0.00001
|
NM_001291303.3(FAT4):c.975G>A (p.Ala325=)
|
rs1300312600
|
0.00001
|
NM_001291303.3(FAT4):c.9824T>G (p.Val3275Gly)
|
rs1003091170
|
0.00001
|
GRCh37/hg19 4q28.1(chr4:126249455-126308835)x3
|
|
|
GRCh37/hg19 4q28.1(chr4:126249455-126333397)x3
|
|
|
NC_000004.11:g.(?_126237567)_(126337797_?)dup
|
|
|
NC_000004.11:g.(?_126237567)_(126412923_?)dup
|
|
|
NM_001291303.3(FAT4):c.10002G>A (p.Glu3334=)
|
rs1726044184
|
|
NM_001291303.3(FAT4):c.10003G>A (p.Val3335Ile)
|
|
|
NM_001291303.3(FAT4):c.10006C>T (p.His3336Tyr)
|
|
|
NM_001291303.3(FAT4):c.10010A>G (p.Tyr3337Cys)
|
|
|
NM_001291303.3(FAT4):c.10011T>G (p.Tyr3337Ter)
|
|
|
NM_001291303.3(FAT4):c.10022G>A (p.Gly3341Asp)
|
|
|
NM_001291303.3(FAT4):c.10025A>G (p.Asn3342Ser)
|
|
|
NM_001291303.3(FAT4):c.10030C>T (p.Arg3344Ter)
|
|
|
NM_001291303.3(FAT4):c.10053T>C (p.Asn3351=)
|
rs554495862
|
|
NM_001291303.3(FAT4):c.10056G>A (p.Lys3352=)
|
|
|
NM_001291303.3(FAT4):c.10070T>C (p.Ile3357Thr)
|
|
|
NM_001291303.3(FAT4):c.10086T>C (p.Ile3362=)
|
rs2126060364
|
|
NM_001291303.3(FAT4):c.10092T>C (p.Asp3364=)
|
|
|
NM_001291303.3(FAT4):c.10093C>A (p.Arg3365=)
|
rs2126060372
|
|
NM_001291303.3(FAT4):c.10098A>G (p.Glu3366=)
|
|
|
NM_001291303.3(FAT4):c.10113G>A (p.Val3371=)
|
|
|
NM_001291303.3(FAT4):c.10125A>G (p.Val3375=)
|
|
|
NM_001291303.3(FAT4):c.10128G>A (p.Leu3376=)
|
|
|
NM_001291303.3(FAT4):c.10145G>A (p.Ser3382Asn)
|
rs759749398
|
|
NM_001291303.3(FAT4):c.10148_10149delinsCA (p.Ile3383Thr)
|
rs2126060437
|
|
NM_001291303.3(FAT4):c.10149T>C (p.Ile3383=)
|
|
|
NM_001291303.3(FAT4):c.1014G>A (p.Glu338=)
|
|
|
NM_001291303.3(FAT4):c.1014G>T (p.Glu338Asp)
|
|
|
NM_001291303.3(FAT4):c.10155T>A (p.Gly3385=)
|
rs780130895
|
|
NM_001291303.3(FAT4):c.10157C>A (p.Ala3386Glu)
|
|
|
NM_001291303.3(FAT4):c.10186A>T (p.Thr3396Ser)
|
|
|
NM_001291303.3(FAT4):c.10199C>T (p.Ala3400Val)
|
rs1553927211
|
|
NM_001291303.3(FAT4):c.10206C>T (p.Asp3402=)
|
rs2126060513
|
|
NM_001291303.3(FAT4):c.10239G>A (p.Val3413=)
|
|
|
NM_001291303.3(FAT4):c.10247G>C (p.Ser3416Thr)
|
|
|
NM_001291303.3(FAT4):c.10261A>G (p.Ile3421Val)
|
|
|
NM_001291303.3(FAT4):c.10261A>T (p.Ile3421Leu)
|
|
|
NM_001291303.3(FAT4):c.10271A>G (p.His3424Arg)
|
rs561616799
|
|
NM_001291303.3(FAT4):c.10276A>G (p.Thr3426Ala)
|
rs2126060621
|
|
NM_001291303.3(FAT4):c.10284C>T (p.Val3428=)
|
|
|
NM_001291303.3(FAT4):c.10308C>T (p.Ile3436=)
|
|
|
NM_001291303.3(FAT4):c.10310C>G (p.Pro3437Arg)
|
|
|
NM_001291303.3(FAT4):c.1032G>A (p.Leu344=)
|
|
|
NM_001291303.3(FAT4):c.10336A>T (p.Ile3446Phe)
|
|
|
NM_001291303.3(FAT4):c.10338C>G (p.Ile3446Met)
|
|
|
NM_001291303.3(FAT4):c.10339G>T (p.Gly3447Ter)
|
|
|
NM_001291303.3(FAT4):c.10350T>C (p.Asn3450=)
|
|
|
NM_001291303.3(FAT4):c.10359T>G (p.Gly3453=)
|
|
|
NM_001291303.3(FAT4):c.10362C>A (p.Ala3454=)
|
|
|
NM_001291303.3(FAT4):c.10376C>T (p.Pro3459Leu)
|
|
|
NM_001291303.3(FAT4):c.10398T>C (p.Val3466=)
|
|
|
NM_001291303.3(FAT4):c.10399A>T (p.Thr3467Ser)
|
|
|
NM_001291303.3(FAT4):c.10407A>G (p.Glu3469=)
|
|
|
NM_001291303.3(FAT4):c.10414C>A (p.Arg3472=)
|
rs1403984745
|
|
NM_001291303.3(FAT4):c.10419A>G (p.Glu3473=)
|
rs1274720931
|
|
NM_001291303.3(FAT4):c.10443A>C (p.Ser3481=)
|
|
|
NM_001291303.3(FAT4):c.10443A>G (p.Ser3481=)
|
|
|
NM_001291303.3(FAT4):c.10446T>G (p.Val3482=)
|
|
|
NM_001291303.3(FAT4):c.10451C>G (p.Ala3484Gly)
|
rs2126060831
|
|
NM_001291303.3(FAT4):c.10455T>A (p.Val3485=)
|
|
|
NM_001291303.3(FAT4):c.10468C>A (p.Pro3490Thr)
|
rs1227571012
|
|
NM_001291303.3(FAT4):c.10483A>G (p.Ser3495Gly)
|
|
|
NM_001291303.3(FAT4):c.10484G>T (p.Ser3495Ile)
|
|
|
NM_001291303.3(FAT4):c.104C>T (p.Pro35Leu)
|
|
|
NM_001291303.3(FAT4):c.10503C>A (p.Thr3501=)
|
|
|
NM_001291303.3(FAT4):c.10512T>C (p.Asp3504=)
|
rs2126060911
|
|
NM_001291303.3(FAT4):c.10524C>T (p.Asn3508=)
|
|
|
NM_001291303.3(FAT4):c.10541T>A (p.Val3514Asp)
|
|
|
NM_001291303.3(FAT4):c.10550_10552del (p.Gly3517del)
|
|
|
NM_001291303.3(FAT4):c.10558A>C (p.Met3520Leu)
|
|
|
NM_001291303.3(FAT4):c.10578C>A (p.Gly3526=)
|
|
|
NM_001291303.3(FAT4):c.10592C>A (p.Thr3531Asn)
|
rs1726076353
|
|
NM_001291303.3(FAT4):c.10593C>G (p.Thr3531=)
|
|
|
NM_001291303.3(FAT4):c.10594C>T (p.Leu3532Phe)
|
|
|
NM_001291303.3(FAT4):c.10598A>T (p.Gln3533Leu)
|
|
|
NM_001291303.3(FAT4):c.1059G>A (p.Val353=)
|
|
|
NM_001291303.3(FAT4):c.105G>C (p.Pro35=)
|
rs1730597475
|
|
NM_001291303.3(FAT4):c.10615C>A (p.Leu3539Ile)
|
|
|
NM_001291303.3(FAT4):c.10615C>T (p.Leu3539Phe)
|
|
|
NM_001291303.3(FAT4):c.10620T>A (p.Pro3540=)
|
|
|
NM_001291303.3(FAT4):c.10626T>C (p.Asn3542=)
|
|
|
NM_001291303.3(FAT4):c.10634C>T (p.Pro3545Leu)
|
|
|
NM_001291303.3(FAT4):c.1063T>A (p.Phe355Ile)
|
rs1471671726
|
|
NM_001291303.3(FAT4):c.10641T>A (p.Thr3547=)
|
rs1422968373
|
|
NM_001291303.3(FAT4):c.10653G>A (p.Leu3551=)
|
|
|
NM_001291303.3(FAT4):c.10664C>T (p.Pro3555Leu)
|
|
|
NM_001291303.3(FAT4):c.10676A>G (p.Tyr3559Cys)
|
|
|
NM_001291303.3(FAT4):c.10679T>G (p.Phe3560Cys)
|
rs2126061121
|
|
NM_001291303.3(FAT4):c.10707C>A (p.Ser3569Arg)
|
|
|
NM_001291303.3(FAT4):c.10713C>A (p.Thr3571=)
|
|
|
NM_001291303.3(FAT4):c.10717G>C (p.Glu3573Gln)
|
|
|
NM_001291303.3(FAT4):c.10720A>G (p.Ile3574Val)
|
|
|
NM_001291303.3(FAT4):c.10743C>A (p.Asp3581Glu)
|
|
|
NM_001291303.3(FAT4):c.10746C>T (p.Phe3582=)
|
|
|
NM_001291303.3(FAT4):c.10752G>A (p.Leu3584=)
|
|
|
NM_001291303.3(FAT4):c.10759G>A (p.Val3587Ile)
|
|
|
NM_001291303.3(FAT4):c.10762A>G (p.Thr3588Ala)
|
rs1187751054
|
|
NM_001291303.3(FAT4):c.10767G>A (p.Lys3589=)
|
rs139021655
|
|
NM_001291303.3(FAT4):c.10769A>T (p.Asp3590Val)
|
|
|
NM_001291303.3(FAT4):c.1076C>T (p.Pro359Leu)
|
|
|
NM_001291303.3(FAT4):c.1077G>A (p.Pro359=)
|
|
|
NM_001291303.3(FAT4):c.10788G>A (p.Met3596Ile)
|
rs1447514638
|
|
NM_001291303.3(FAT4):c.10801A>G (p.Thr3601Ala)
|
|
|
NM_001291303.3(FAT4):c.10806G>A (p.Val3602=)
|
|
|
NM_001291303.3(FAT4):c.10819A>G (p.Ile3607Val)
|
rs945820499
|
|
NM_001291303.3(FAT4):c.10834A>C (p.Asn3612His)
|
|
|
NM_001291303.3(FAT4):c.10842A>G (p.Ser3614=)
|
|
|
NM_001291303.3(FAT4):c.10850G>A (p.Arg3617Gln)
|
|
|
NM_001291303.3(FAT4):c.10852A>G (p.Thr3618Ala)
|
rs1726090881
|
|
NM_001291303.3(FAT4):c.10854G>A (p.Thr3618=)
|
|
|
NM_001291303.3(FAT4):c.1085C>G (p.Ser362Trp)
|
|
|
NM_001291303.3(FAT4):c.10860G>A (p.Glu3620=)
|
|
|
NM_001291303.3(FAT4):c.10861A>C (p.Ile3621Leu)
|
rs769926658
|
|
NM_001291303.3(FAT4):c.10869T>A (p.Val3623=)
|
rs2126061368
|
|
NM_001291303.3(FAT4):c.1086G>T (p.Ser362=)
|
|
|
NM_001291303.3(FAT4):c.10871A>G (p.Asn3624Ser)
|
|
|
NM_001291303.3(FAT4):c.10872T>C (p.Asn3624=)
|
rs1726092616
|
|
NM_001291303.3(FAT4):c.10881T>A (p.Gly3627=)
|
|
|
NM_001291303.3(FAT4):c.10881T>G (p.Gly3627=)
|
|
|
NM_001291303.3(FAT4):c.10893C>G (p.Pro3631=)
|
|
|
NM_001291303.3(FAT4):c.10893C>T (p.Pro3631=)
|
|
|
NM_001291303.3(FAT4):c.10894G>A (p.Gly3632Ser)
|
|
|
NM_001291303.3(FAT4):c.10899G>T (p.Gly3633=)
|
|
|
NM_001291303.3(FAT4):c.1089C>G (p.Arg363=)
|
rs566345927
|
|
NM_001291303.3(FAT4):c.10908C>T (p.Gly3636=)
|
|
|
NM_001291303.3(FAT4):c.10910C>T (p.Ser3637Phe)
|
rs1332535204
|
|
NM_001291303.3(FAT4):c.1092C>T (p.Tyr364=)
|
rs1730667393
|
|
NM_001291303.3(FAT4):c.10935G>A (p.Val3645=)
|
rs758367201
|
|
NM_001291303.3(FAT4):c.10935G>T (p.Val3645=)
|
rs758367201
|
|
NM_001291303.3(FAT4):c.10936T>G (p.Leu3646Val)
|
|
|
NM_001291303.3(FAT4):c.10957C>T (p.Leu3653Phe)
|
|
|
NM_001291303.3(FAT4):c.1095C>A (p.Ala365=)
|
rs2125939679
|
|
NM_001291303.3(FAT4):c.10965A>G (p.Ser3655=)
|
|
|
NM_001291303.3(FAT4):c.10974C>G (p.Thr3658=)
|
rs567783118
|
|
NM_001291303.3(FAT4):c.10974C>T (p.Thr3658=)
|
|
|
NM_001291303.3(FAT4):c.10992A>C (p.Pro3664=)
|
|
|
NM_001291303.3(FAT4):c.10992A>G (p.Pro3664=)
|
|
|
NM_001291303.3(FAT4):c.11005G>C (p.Asp3669His)
|
rs2126061545
|
|
NM_001291303.3(FAT4):c.1104T>C (p.Asp368=)
|
|
|
NM_001291303.3(FAT4):c.11055C>T (p.Val3685=)
|
|
|
NM_001291303.3(FAT4):c.11074C>T (p.His3692Tyr)
|
|
|
NM_001291303.3(FAT4):c.1107G>A (p.Glu369=)
|
rs1578512638
|
|
NM_001291303.3(FAT4):c.11081C>T (p.Thr3694Ile)
|
|
|
NM_001291303.3(FAT4):c.11088G>A (p.Thr3696=)
|
rs368928868
|
|
NM_001291303.3(FAT4):c.11096T>C (p.Ile3699Thr)
|
|
|
NM_001291303.3(FAT4):c.11097C>A (p.Ile3699=)
|
|
|
NM_001291303.3(FAT4):c.11097C>T (p.Ile3699=)
|
|
|
NM_001291303.3(FAT4):c.11100A>G (p.Arg3700=)
|
|
|
NM_001291303.3(FAT4):c.11123A>G (p.Asn3708Ser)
|
|
|
NM_001291303.3(FAT4):c.11139C>T (p.Asn3713=)
|
|
|
NM_001291303.3(FAT4):c.11160C>A (p.Gly3720=)
|
|
|
NM_001291303.3(FAT4):c.11160C>T (p.Gly3720=)
|
|
|
NM_001291303.3(FAT4):c.11161G>A (p.Val3721Ile)
|
rs557732280
|
|
NM_001291303.3(FAT4):c.11163A>G (p.Val3721=)
|
rs2126061767
|
|
NM_001291303.3(FAT4):c.11165C>G (p.Pro3722Arg)
|
rs2126061781
|
|
NM_001291303.3(FAT4):c.1116A>G (p.Gln372=)
|
|
|
NM_001291303.3(FAT4):c.11182T>C (p.Leu3728=)
|
|
|
NM_001291303.3(FAT4):c.11190C>T (p.Asn3730=)
|
|
|
NM_001291303.3(FAT4):c.11208A>G (p.Leu3736=)
|
|
|
NM_001291303.3(FAT4):c.11210G>A (p.Arg3737His)
|
|
|
NM_001291303.3(FAT4):c.11246C>T (p.Ala3749Val)
|
rs1056083552
|
|
NM_001291303.3(FAT4):c.11290C>A (p.Leu3764Ile)
|
|
|
NM_001291303.3(FAT4):c.11307G>A (p.Lys3769=)
|
|
|
NM_001291303.3(FAT4):c.11324A>G (p.Tyr3775Cys)
|
rs1341896601
|
|
NM_001291303.3(FAT4):c.11340C>T (p.Gly3780=)
|
|
|
NM_001291303.3(FAT4):c.11347A>G (p.Thr3783Ala)
|
|
|
NM_001291303.3(FAT4):c.11352C>T (p.Phe3784=)
|
|
|
NM_001291303.3(FAT4):c.11360G>A (p.Ser3787Asn)
|
|
|
NM_001291303.3(FAT4):c.11368G>A (p.Glu3790Lys)
|
|
|
NM_001291303.3(FAT4):c.11384A>G (p.Gln3795Arg)
|
|
|
NM_001291303.3(FAT4):c.11411A>G (p.Asp3804Gly)
|
rs2126062121
|
|
NM_001291303.3(FAT4):c.11433C>T (p.Gly3811=)
|
|
|
NM_001291303.3(FAT4):c.1143C>T (p.Thr381=)
|
|
|
NM_001291303.3(FAT4):c.11461C>T (p.Arg3821Ter)
|
rs398122957
|
|
NM_001291303.3(FAT4):c.11481C>T (p.Ser3827=)
|
|
|
NM_001291303.3(FAT4):c.1148C>A (p.Thr383Lys)
|
|
|
NM_001291303.3(FAT4):c.1148C>T (p.Thr383Met)
|
|
|
NM_001291303.3(FAT4):c.11492G>C (p.Ser3831Thr)
|
|
|
NM_001291303.3(FAT4):c.11495G>A (p.Arg3832His)
|
|
|
NM_001291303.3(FAT4):c.11498A>G (p.Glu3833Gly)
|
|
|
NM_001291303.3(FAT4):c.11514C>T (p.Ile3838=)
|
|
|
NM_001291303.3(FAT4):c.11517C>G (p.Ile3839Met)
|
|
|
NM_001291303.3(FAT4):c.11517C>T (p.Ile3839=)
|
|
|
NM_001291303.3(FAT4):c.11531C>T (p.Pro3844Leu)
|
rs142291617
|
|
NM_001291303.3(FAT4):c.11535G>A (p.Leu3845=)
|
rs2126062311
|
|
NM_001291303.3(FAT4):c.11562A>G (p.Pro3854=)
|
|
|
NM_001291303.3(FAT4):c.11565A>T (p.Gly3855=)
|
|
|
NM_001291303.3(FAT4):c.11569G>A (p.Ala3857Thr)
|
|
|
NM_001291303.3(FAT4):c.11587A>G (p.Ile3863Val)
|
rs2126062361
|
|
NM_001291303.3(FAT4):c.11592T>C (p.Asp3864=)
|
|
|
NM_001291303.3(FAT4):c.115T>C (p.Trp39Arg)
|
rs2125938253
|
|
NM_001291303.3(FAT4):c.11639A>G (p.His3880Arg)
|
|
|
NM_001291303.3(FAT4):c.1164C>T (p.Pro388=)
|
|
|
NM_001291303.3(FAT4):c.1167G>A (p.Ala389=)
|
|
|
NM_001291303.3(FAT4):c.11687G>A (p.Gly3896Asp)
|
|
|
NM_001291303.3(FAT4):c.11724G>A (p.Gln3908=)
|
|
|
NM_001291303.3(FAT4):c.11745C>T (p.Ala3915=)
|
|
|
NM_001291303.3(FAT4):c.11748C>T (p.Ile3916=)
|
|
|
NM_001291303.3(FAT4):c.1174G>A (p.Gly392Arg)
|
|
|
NM_001291303.3(FAT4):c.11755A>G (p.Asn3919Asp)
|
rs762329383
|
|
NM_001291303.3(FAT4):c.11768G>C (p.Ser3923Thr)
|
|
|
NM_001291303.3(FAT4):c.11769C>T (p.Ser3923=)
|
|
|
NM_001291303.3(FAT4):c.1176G>C (p.Gly392=)
|
|
|
NM_001291303.3(FAT4):c.11778T>C (p.Cys3926=)
|
|
|
NM_001291303.3(FAT4):c.11784C>T (p.Cys3928=)
|
|
|
NM_001291303.3(FAT4):c.11792G>T (p.Gly3931Val)
|
rs777754541
|
|
NM_001291303.3(FAT4):c.11797A>G (p.Thr3933Ala)
|
|
|
NM_001291303.3(FAT4):c.11800+16T>A
|
rs1301881204
|
|
NM_001291303.3(FAT4):c.11801-7A>G
|
|
|
NM_001291303.3(FAT4):c.11801-8T>C
|
|
|
NM_001291303.3(FAT4):c.11808G>T (p.Met3936Ile)
|
|
|
NM_001291303.3(FAT4):c.11815T>C (p.Ser3939Pro)
|
|
|
NM_001291303.3(FAT4):c.11820A>T (p.Ser3940=)
|
|
|
NM_001291303.3(FAT4):c.11825A>G (p.Asn3942Ser)
|
|
|
NM_001291303.3(FAT4):c.11826_11828dup (p.Tyr3943_Cys3944insTyr)
|
|
|
NM_001291303.3(FAT4):c.11831G>A (p.Cys3944Tyr)
|
|
|
NM_001291303.3(FAT4):c.11843C>T (p.Pro3948Leu)
|
rs1165953776
|
|
NM_001291303.3(FAT4):c.11859T>G (p.Gly3953=)
|
|
|
NM_001291303.3(FAT4):c.1186G>A (p.Val396Met)
|
|
|
NM_001291303.3(FAT4):c.11870G>A (p.Ser3957Asn)
|
|
|
NM_001291303.3(FAT4):c.11885ATT[1] (p.Tyr3963del)
|
rs766475561
|
|
NM_001291303.3(FAT4):c.11886T>C (p.Tyr3962=)
|
rs2126071598
|
|
NM_001291303.3(FAT4):c.11900C>A (p.Pro3967Gln)
|
|
|
NM_001291303.3(FAT4):c.11901A>G (p.Pro3967=)
|
rs564401312
|
|
NM_001291303.3(FAT4):c.11905+12T>C
|
|
|
NM_001291303.3(FAT4):c.11905+12T>G
|
|
|
NM_001291303.3(FAT4):c.11905+17T>G
|
|
|
NM_001291303.3(FAT4):c.11906-282C>T
|
rs115018218
|
|
NM_001291303.3(FAT4):c.11906-40A>G
|
rs6814158
|
|
NM_001291303.3(FAT4):c.11906-4del
|
|
|
NM_001291303.3(FAT4):c.11906-5A>G
|
|
|
NM_001291303.3(FAT4):c.11906-7C>T
|
|
|
NM_001291303.3(FAT4):c.11907T>A (p.Gly3969=)
|
|
|
NM_001291303.3(FAT4):c.11916A>G (p.Gly3972=)
|
|
|
NM_001291303.3(FAT4):c.11925C>T (p.Cys3975=)
|
|
|
NM_001291303.3(FAT4):c.11927A>G (p.Glu3976Gly)
|
|
|
NM_001291303.3(FAT4):c.11931G>C (p.Leu3977Phe)
|
|
|
NM_001291303.3(FAT4):c.11943A>C (p.Gly3981=)
|
rs754755525
|
|
NM_001291303.3(FAT4):c.11945T>G (p.Phe3982Cys)
|
|
|
NM_001291303.3(FAT4):c.11959T>C (p.Tyr3987His)
|
rs2126076080
|
|
NM_001291303.3(FAT4):c.1195C>A (p.Leu399Ile)
|
|
|
NM_001291303.3(FAT4):c.11966A>C (p.Glu3989Ala)
|
rs2126076090
|
|
NM_001291303.3(FAT4):c.11967A>G (p.Glu3989=)
|
rs2126076092
|
|
NM_001291303.3(FAT4):c.11969T>C (p.Phe3990Ser)
|
|
|
NM_001291303.3(FAT4):c.12002A>C (p.Tyr4001Ser)
|
|
|
NM_001291303.3(FAT4):c.12006C>T (p.Val4002=)
|
|
|
NM_001291303.3(FAT4):c.12018G>A (p.Thr4006=)
|
|
|
NM_001291303.3(FAT4):c.12019A>G (p.Ile4007Val)
|
rs913813636
|
|
NM_001291303.3(FAT4):c.12029A>G (p.His4010Arg)
|
|
|
NM_001291303.3(FAT4):c.12037T>C (p.Leu4013=)
|
|
|
NM_001291303.3(FAT4):c.12045C>T (p.Tyr4015=)
|
|
|
NM_001291303.3(FAT4):c.12051T>C (p.Tyr4017=)
|
|
|
NM_001291303.3(FAT4):c.12067G>A (p.Asp4023Asn)
|
rs372001379
|
|
NM_001291303.3(FAT4):c.12069C>T (p.Asp4023=)
|
|
|
NM_001291303.3(FAT4):c.1206T>C (p.Asn402=)
|
|
|
NM_001291303.3(FAT4):c.12078G>A (p.Glu4026=)
|
rs2126076258
|
|
NM_001291303.3(FAT4):c.12082T>C (p.Leu4028=)
|
|
|
NM_001291303.3(FAT4):c.12091G>A (p.Glu4031Lys)
|
rs1085307886
|
|
NM_001291303.3(FAT4):c.12093A>T (p.Glu4031Asp)
|
rs2126076276
|
|
NM_001291303.3(FAT4):c.12097G>A (p.Ala4033Thr)
|
rs1328584807
|
|
NM_001291303.3(FAT4):c.12099C>A (p.Ala4033=)
|
|
|
NM_001291303.3(FAT4):c.120C>T (p.Val40=)
|
|
|
NM_001291303.3(FAT4):c.12117C>T (p.Phe4039=)
|
|
|
NM_001291303.3(FAT4):c.1212G>T (p.Gln404His)
|
|
|
NM_001291303.3(FAT4):c.12131G>A (p.Gly4044Asp)
|
rs760328375
|
|
NM_001291303.3(FAT4):c.12142T>A (p.Tyr4048Asn)
|
|
|
NM_001291303.3(FAT4):c.12157A>G (p.Met4053Val)
|
|
|
NM_001291303.3(FAT4):c.12168G>T (p.Val4056=)
|
|
|
NM_001291303.3(FAT4):c.12180T>C (p.His4060=)
|
|
|
NM_001291303.3(FAT4):c.1218C>T (p.His406=)
|
|
|
NM_001291303.3(FAT4):c.12213+18A>T
|
|
|
NM_001291303.3(FAT4):c.12213+19TTG[2]
|
|
|
NM_001291303.3(FAT4):c.12213+8A>G
|
|
|
NM_001291303.3(FAT4):c.12214-11T>C
|
|
|
NM_001291303.3(FAT4):c.12214-20T>G
|
|
|
NM_001291303.3(FAT4):c.12214-3T>C
|
|
|
NM_001291303.3(FAT4):c.12214-42G>C
|
rs180692127
|
|
NM_001291303.3(FAT4):c.12214-9G>T
|
|
|
NM_001291303.3(FAT4):c.12234C>T (p.Asp4078=)
|
|
|
NM_001291303.3(FAT4):c.12240T>C (p.Cys4080=)
|
|
|
NM_001291303.3(FAT4):c.12240_12244del (p.Cys4080_Glu4082delinsTer)
|
|
|
NM_001291303.3(FAT4):c.12243T>C (p.Ser4081=)
|
|
|
NM_001291303.3(FAT4):c.12262T>C (p.Tyr4088His)
|
|
|
NM_001291303.3(FAT4):c.12271G>C (p.Val4091Leu)
|
rs2126082991
|
|
NM_001291303.3(FAT4):c.12276T>C (p.Ser4092=)
|
|
|
NM_001291303.3(FAT4):c.1227G>T (p.Val409=)
|
|
|
NM_001291303.3(FAT4):c.12299+17G>A
|
|
|
NM_001291303.3(FAT4):c.12300-14C>T
|
rs2126083657
|
|
NM_001291303.3(FAT4):c.12300-18C>A
|
|
|
NM_001291303.3(FAT4):c.12300-6A>C
|
rs2126083663
|
|
NM_001291303.3(FAT4):c.12301A>T (p.Thr4101Ser)
|
|
|
NM_001291303.3(FAT4):c.12310G>A (p.Val4104Ile)
|
rs2126083675
|
|
NM_001291303.3(FAT4):c.12318A>C (p.Pro4106=)
|
|
|
NM_001291303.3(FAT4):c.12323G>A (p.Arg4108Lys)
|
|
|
NM_001291303.3(FAT4):c.12327T>A (p.Val4109=)
|
|
|
NM_001291303.3(FAT4):c.12347C>T (p.Ser4116Phe)
|
rs1560631602
|
|
NM_001291303.3(FAT4):c.12361C>T (p.Leu4121Phe)
|
|
|
NM_001291303.3(FAT4):c.12366G>A (p.Gln4122=)
|
|
|
NM_001291303.3(FAT4):c.12378C>T (p.His4126=)
|
|
|
NM_001291303.3(FAT4):c.12381G>T (p.Val4127=)
|
|
|
NM_001291303.3(FAT4):c.12385A>G (p.Ser4129Gly)
|
|
|
NM_001291303.3(FAT4):c.12386G>A (p.Ser4129Asn)
|
|
|
NM_001291303.3(FAT4):c.12389A>C (p.His4130Pro)
|
|
|
NM_001291303.3(FAT4):c.12390T>A (p.His4130Gln)
|
|
|
NM_001291303.3(FAT4):c.12400G>A (p.Gly4134Arg)
|
rs766004499
|
|
NM_001291303.3(FAT4):c.12402G>A (p.Gly4134=)
|
rs2126083803
|
|
NM_001291303.3(FAT4):c.12416T>C (p.Phe4139Ser)
|
|
|
NM_001291303.3(FAT4):c.12419C>T (p.Ala4140Val)
|
|
|
NM_001291303.3(FAT4):c.12426T>C (p.Asn4142=)
|
|
|
NM_001291303.3(FAT4):c.12431G>A (p.Arg4144Lys)
|
|
|
NM_001291303.3(FAT4):c.12435T>C (p.Pro4145=)
|
|
|
NM_001291303.3(FAT4):c.12436C>T (p.Leu4146=)
|
|
|
NM_001291303.3(FAT4):c.1245G>T (p.Pro415=)
|
rs1578512903
|
|
NM_001291303.3(FAT4):c.12464A>C (p.Gln4155Pro)
|
|
|
NM_001291303.3(FAT4):c.12475G>T (p.Asp4159Tyr)
|
rs141297199
|
|
NM_001291303.3(FAT4):c.12479+20T>C
|
|
|
NM_001291303.3(FAT4):c.12479+211AT[8]
|
rs34261234
|
|
NM_001291303.3(FAT4):c.12479+211AT[9]
|
rs34261234
|
|
NM_001291303.3(FAT4):c.12479+228_12479+229insGT
|
rs35665579
|
|
NM_001291303.3(FAT4):c.12479+4T>C
|
rs775906121
|
|
NM_001291303.3(FAT4):c.12480-119del
|
rs139775489
|
|
NM_001291303.3(FAT4):c.12480-4T>C
|
|
|
NM_001291303.3(FAT4):c.12486T>C (p.Pro4162=)
|
|
|
NM_001291303.3(FAT4):c.124G>C (p.Gly42Arg)
|
|
|
NM_001291303.3(FAT4):c.12501T>C (p.Ala4167=)
|
rs2126085872
|
|
NM_001291303.3(FAT4):c.12509G>A (p.Arg4170His)
|
|
|
NM_001291303.3(FAT4):c.12509G>C (p.Arg4170Pro)
|
rs758666028
|
|
NM_001291303.3(FAT4):c.12510C>T (p.Arg4170=)
|
|
|
NM_001291303.3(FAT4):c.12513C>T (p.Ser4171=)
|
|
|
NM_001291303.3(FAT4):c.12524A>G (p.His4175Arg)
|
|
|
NM_001291303.3(FAT4):c.12525T>C (p.His4175=)
|
|
|
NM_001291303.3(FAT4):c.12532A>T (p.Thr4178Ser)
|
|
|
NM_001291303.3(FAT4):c.12537T>C (p.Cys4179=)
|
|
|
NM_001291303.3(FAT4):c.12547T>C (p.Trp4183Arg)
|
|
|
NM_001291303.3(FAT4):c.1254C>T (p.Ser418=)
|
rs781465335
|
|
NM_001291303.3(FAT4):c.12559C>G (p.Gln4187Glu)
|
|
|
NM_001291303.3(FAT4):c.12567T>C (p.His4189=)
|
|
|
NM_001291303.3(FAT4):c.12589A>G (p.Lys4197Glu)
|
|
|
NM_001291303.3(FAT4):c.1258A>G (p.Ile420Val)
|
rs2125939948
|
|
NM_001291303.3(FAT4):c.12604+10G>T
|
|
|
NM_001291303.3(FAT4):c.12604+20T>C
|
|
|
NM_001291303.3(FAT4):c.12604+9G>A
|
rs1190206749
|
|
NM_001291303.3(FAT4):c.12620C>G (p.Thr4207Ser)
|
|
|
NM_001291303.3(FAT4):c.12622G>T (p.Ala4208Ser)
|
|
|
NM_001291303.3(FAT4):c.12644G>C (p.Gly4215Ala)
|
rs2126087162
|
|
NM_001291303.3(FAT4):c.12646C>T (p.Arg4216Cys)
|
|
|
NM_001291303.3(FAT4):c.12676A>C (p.Lys4226Gln)
|
|
|
NM_001291303.3(FAT4):c.12678G>A (p.Lys4226=)
|
rs2126087199
|
|
NM_001291303.3(FAT4):c.12679C>T (p.Arg4227Trp)
|
|
|
NM_001291303.3(FAT4):c.12686_12687dup (p.Leu4230fs)
|
|
|
NM_001291303.3(FAT4):c.12687T>C (p.Tyr4229=)
|
|
|
NM_001291303.3(FAT4):c.12702C>T (p.Ser4234=)
|
|
|
NM_001291303.3(FAT4):c.12705A>G (p.Leu4235=)
|
|
|
NM_001291303.3(FAT4):c.12726T>C (p.Pro4242=)
|
|
|
NM_001291303.3(FAT4):c.1273G>T (p.Ala425Ser)
|
rs138548779
|
|
NM_001291303.3(FAT4):c.12742C>A (p.Leu4248Met)
|
|
|
NM_001291303.3(FAT4):c.1275C>T (p.Ala425=)
|
|
|
NM_001291303.3(FAT4):c.12776G>A (p.Gly4259Asp)
|
|
|
NM_001291303.3(FAT4):c.12781T>G (p.Leu4261Val)
|
|
|
NM_001291303.3(FAT4):c.12795A>G (p.Gln4265=)
|
|
|
NM_001291303.3(FAT4):c.12806A>G (p.Asn4269Ser)
|
|
|
NM_001291303.3(FAT4):c.12822+12G>A
|
|
|
NM_001291303.3(FAT4):c.12823-10T>C
|
|
|
NM_001291303.3(FAT4):c.12823-15T>A
|
|
|
NM_001291303.3(FAT4):c.12823-4A>G
|
|
|
NM_001291303.3(FAT4):c.12840A>G (p.Val4280=)
|
|
|
NM_001291303.3(FAT4):c.12849A>G (p.Thr4283=)
|
|
|
NM_001291303.3(FAT4):c.12886A>G (p.Ile4296Val)
|
|
|
NM_001291303.3(FAT4):c.12898T>C (p.Tyr4300His)
|
|
|
NM_001291303.3(FAT4):c.12908A>T (p.Asp4303Val)
|
rs2126092920
|
|
NM_001291303.3(FAT4):c.1291A>C (p.Ile431Leu)
|
rs2125940000
|
|
NM_001291303.3(FAT4):c.12932T>C (p.Ile4311Thr)
|
|
|
NM_001291303.3(FAT4):c.12934G>T (p.Gly4312Trp)
|
|
|
NM_001291303.3(FAT4):c.12958T>C (p.Leu4320=)
|
|
|
NM_001291303.3(FAT4):c.12963T>C (p.Ser4321=)
|
|
|
NM_001291303.3(FAT4):c.12982A>G (p.Arg4328Gly)
|
|
|
NM_001291303.3(FAT4):c.12983G>A (p.Arg4328Lys)
|
|
|
NM_001291303.3(FAT4):c.12992T>C (p.Ile4331Thr)
|
|
|
NM_001291303.3(FAT4):c.12994C>T (p.His4332Tyr)
|
|
|
NM_001291303.3(FAT4):c.13012G>A (p.Gly4338Ser)
|
|
|
NM_001291303.3(FAT4):c.13017C>T (p.Gly4339=)
|
|
|
NM_001291303.3(FAT4):c.13033A>G (p.Ile4345Val)
|
|
|
NM_001291303.3(FAT4):c.13044A>T (p.Gly4348=)
|
|
|
NM_001291303.3(FAT4):c.13058A>G (p.Asn4353Ser)
|
rs2126093199
|
|
NM_001291303.3(FAT4):c.13065A>G (p.Ala4355=)
|
|
|
NM_001291303.3(FAT4):c.13075_13076delinsAT (p.Ala4359Ile)
|
|
|
NM_001291303.3(FAT4):c.13077C>A (p.Ala4359=)
|
|
|
NM_001291303.3(FAT4):c.13080A>G (p.Gln4360=)
|
|
|
NM_001291303.3(FAT4):c.13084+13A>G
|
rs984882284
|
|
NM_001291303.3(FAT4):c.13084+14_13084+20del
|
|
|
NM_001291303.3(FAT4):c.13084+18G>A
|
|
|
NM_001291303.3(FAT4):c.13084+19T>G
|
|
|
NM_001291303.3(FAT4):c.13084+7G>A
|
|
|
NM_001291303.3(FAT4):c.13084+9C>T
|
|
|
NM_001291303.3(FAT4):c.13085-16CTT[2]
|
|
|
NM_001291303.3(FAT4):c.13085-9T>C
|
|
|
NM_001291303.3(FAT4):c.13097G>T (p.Gly4366Val)
|
|
|
NM_001291303.3(FAT4):c.13113G>T (p.Met4371Ile)
|
|
|
NM_001291303.3(FAT4):c.13155C>T (p.Ser4385=)
|
|
|
NM_001291303.3(FAT4):c.13161C>T (p.Ala4387=)
|
|
|
NM_001291303.3(FAT4):c.13169C>T (p.Ser4390Leu)
|
|
|
NM_001291303.3(FAT4):c.13176A>T (p.Thr4392=)
|
|
|
NM_001291303.3(FAT4):c.13179T>A (p.Asp4393Glu)
|
|
|
NM_001291303.3(FAT4):c.1317C>T (p.Ser439=)
|
|
|
NM_001291303.3(FAT4):c.13197C>G (p.Gly4399=)
|
rs2126096129
|
|
NM_001291303.3(FAT4):c.13221C>T (p.Ala4407=)
|
|
|
NM_001291303.3(FAT4):c.13223G>A (p.Ser4408Asn)
|
rs2126096178
|
|
NM_001291303.3(FAT4):c.13227C>T (p.Asn4409=)
|
rs550455897
|
|
NM_001291303.3(FAT4):c.13228C>A (p.Pro4410Thr)
|
|
|
NM_001291303.3(FAT4):c.13242T>C (p.Asp4414=)
|
|
|
NM_001291303.3(FAT4):c.13248G>A (p.Leu4416=)
|
|
|
NM_001291303.3(FAT4):c.13254T>C (p.Ile4418=)
|
rs1727561886
|
|
NM_001291303.3(FAT4):c.13254T>G (p.Ile4418Met)
|
rs1727561886
|
|
NM_001291303.3(FAT4):c.13274G>A (p.Arg4425Lys)
|
|
|
NM_001291303.3(FAT4):c.1328A>G (p.Asn443Ser)
|
rs1013842967
|
|
NM_001291303.3(FAT4):c.13292A>T (p.Asp4431Val)
|
rs774943740
|
|
NM_001291303.3(FAT4):c.13305C>T (p.His4435=)
|
rs1357034003
|
|
NM_001291303.3(FAT4):c.13310G>A (p.Cys4437Tyr)
|
rs2126096288
|
|
NM_001291303.3(FAT4):c.1332C>T (p.Tyr444=)
|
rs1730689505
|
|
NM_001291303.3(FAT4):c.13350C>T (p.Gly4450=)
|
|
|
NM_001291303.3(FAT4):c.13365C>T (p.Cys4455=)
|
rs1727567219
|
|
NM_001291303.3(FAT4):c.13371C>T (p.Asp4457=)
|
|
|
NM_001291303.3(FAT4):c.13372T>C (p.Ser4458Pro)
|
|
|
NM_001291303.3(FAT4):c.1337C>T (p.Ala446Val)
|
|
|
NM_001291303.3(FAT4):c.13380G>A (p.Thr4460=)
|
|
|
NM_001291303.3(FAT4):c.13401G>A (p.Val4467=)
|
rs1257989050
|
|
NM_001291303.3(FAT4):c.13416C>G (p.Gly4472=)
|
|
|
NM_001291303.3(FAT4):c.13431G>A (p.Gln4477=)
|
|
|
NM_001291303.3(FAT4):c.13444A>C (p.Lys4482Gln)
|
|
|
NM_001291303.3(FAT4):c.13454G>A (p.Ser4485Asn)
|
|
|
NM_001291303.3(FAT4):c.1345G>C (p.Gly449Arg)
|
|
|
NM_001291303.3(FAT4):c.13460C>A (p.Ala4487Glu)
|
|
|
NM_001291303.3(FAT4):c.13461G>A (p.Ala4487=)
|
rs776669972
|
|
NM_001291303.3(FAT4):c.13462G>A (p.Gly4488Arg)
|
|
|
NM_001291303.3(FAT4):c.13463G>T (p.Gly4488Val)
|
|
|
NM_001291303.3(FAT4):c.13467T>C (p.His4489=)
|
|
|
NM_001291303.3(FAT4):c.13468G>A (p.Val4490Ile)
|
|
|
NM_001291303.3(FAT4):c.13481G>C (p.Ser4494Thr)
|
|
|
NM_001291303.3(FAT4):c.13498A>T (p.Ile4500Phe)
|
rs2126096628
|
|
NM_001291303.3(FAT4):c.134C>A (p.Pro45Gln)
|
|
|
NM_001291303.3(FAT4):c.13504C>A (p.Leu4502Met)
|
|
|
NM_001291303.3(FAT4):c.13538G>C (p.Ser4513Thr)
|
|
|
NM_001291303.3(FAT4):c.13542C>T (p.Cys4514=)
|
|
|
NM_001291303.3(FAT4):c.13544C>A (p.Ala4515Glu)
|
|
|
NM_001291303.3(FAT4):c.13548C>A (p.Thr4516=)
|
rs138057366
|
|
NM_001291303.3(FAT4):c.13548C>T (p.Thr4516=)
|
rs138057366
|
|
NM_001291303.3(FAT4):c.13549G>A (p.Val4517Ile)
|
rs142649500
|
|
NM_001291303.3(FAT4):c.13565T>A (p.Val4522Asp)
|
|
|
NM_001291303.3(FAT4):c.13581G>A (p.Leu4527=)
|
rs1245303360
|
|
NM_001291303.3(FAT4):c.13583G>A (p.Cys4528Tyr)
|
rs1560639518
|
|
NM_001291303.3(FAT4):c.1358A>T (p.Gln453Leu)
|
rs6847454
|
|
NM_001291303.3(FAT4):c.13590G>A (p.Gln4530=)
|
rs747634638
|
|
NM_001291303.3(FAT4):c.13591T>C (p.Cys4531Arg)
|
|
|
NM_001291303.3(FAT4):c.13602G>A (p.Lys4534=)
|
|
|
NM_001291303.3(FAT4):c.13606G>A (p.Ala4536Thr)
|
rs1212647138
|
|
NM_001291303.3(FAT4):c.13618A>G (p.Lys4540Glu)
|
|
|
NM_001291303.3(FAT4):c.1361C>A (p.Ala454Glu)
|
rs1374779549
|
|
NM_001291303.3(FAT4):c.13625_13626insAAA (p.Lys4544dup)
|
rs759879911
|
|
NM_001291303.3(FAT4):c.13627A>T (p.Lys4543Ter)
|
rs1553931042
|
|
NM_001291303.3(FAT4):c.13629G>A (p.Lys4543=)
|
|
|
NM_001291303.3(FAT4):c.1362G>T (p.Ala454=)
|
|
|
NM_001291303.3(FAT4):c.13634C>A (p.Pro4545Gln)
|
|
|
NM_001291303.3(FAT4):c.13641G>T (p.Glu4547Asp)
|
|
|
NM_001291303.3(FAT4):c.13641GAA[2] (p.Lys4551del)
|
rs1560639673
|
|
NM_001291303.3(FAT4):c.13652A>G (p.Lys4551Arg)
|
|
|
NM_001291303.3(FAT4):c.13662G>T (p.Glu4554Asp)
|
|
|
NM_001291303.3(FAT4):c.13665C>A (p.Asn4555Lys)
|
|
|
NM_001291303.3(FAT4):c.13668T>C (p.Val4556=)
|
|
|
NM_001291303.3(FAT4):c.13671T>C (p.Ala4557=)
|
|
|
NM_001291303.3(FAT4):c.13678G>A (p.Asp4560Asn)
|
rs770945735
|
|
NM_001291303.3(FAT4):c.13683T>C (p.Pro4561=)
|
rs1255106254
|
|
NM_001291303.3(FAT4):c.13699T>C (p.Tyr4567His)
|
|
|
NM_001291303.3(FAT4):c.13705G>A (p.Asp4569Asn)
|
|
|
NM_001291303.3(FAT4):c.13715C>A (p.Thr4572Asn)
|
|
|
NM_001291303.3(FAT4):c.13716T>C (p.Thr4572=)
|
|
|
NM_001291303.3(FAT4):c.13722G>A (p.Arg4574=)
|
|
|
NM_001291303.3(FAT4):c.13731T>C (p.Pro4577=)
|
|
|
NM_001291303.3(FAT4):c.13755C>A (p.Ile4585=)
|
|
|
NM_001291303.3(FAT4):c.13762A>G (p.Arg4588Gly)
|
|
|
NM_001291303.3(FAT4):c.13773C>T (p.Pro4591=)
|
|
|
NM_001291303.3(FAT4):c.1378A>G (p.Ser460Gly)
|
|
|
NM_001291303.3(FAT4):c.13805A>G (p.His4602Arg)
|
|
|
NM_001291303.3(FAT4):c.1380C>T (p.Ser460=)
|
|
|
NM_001291303.3(FAT4):c.1381C>G (p.Leu461Val)
|
|
|
NM_001291303.3(FAT4):c.13827C>G (p.Ser4609Arg)
|
rs767553555
|
|
NM_001291303.3(FAT4):c.13827C>T (p.Ser4609=)
|
rs767553555
|
|
NM_001291303.3(FAT4):c.13830C>T (p.Ala4610=)
|
|
|
NM_001291303.3(FAT4):c.13854G>C (p.Glu4618Asp)
|
|
|
NM_001291303.3(FAT4):c.13886G>A (p.Ser4629Asn)
|
|
|
NM_001291303.3(FAT4):c.13899G>A (p.Ser4633=)
|
rs267600017
|
|
NM_001291303.3(FAT4):c.1389T>A (p.Ile463=)
|
|
|
NM_001291303.3(FAT4):c.13905A>G (p.Ala4635=)
|
|
|
NM_001291303.3(FAT4):c.13917A>G (p.Gln4639=)
|
|
|
NM_001291303.3(FAT4):c.13925A>G (p.Lys4642Arg)
|
rs2126097301
|
|
NM_001291303.3(FAT4):c.1392T>A (p.Phe464Leu)
|
|
|
NM_001291303.3(FAT4):c.13933C>T (p.Arg4645Cys)
|
|
|
NM_001291303.3(FAT4):c.1396A>G (p.Asn466Asp)
|
|
|
NM_001291303.3(FAT4):c.13978G>A (p.Gly4660Ser)
|
rs746280613
|
|
NM_001291303.3(FAT4):c.13999A>G (p.Met4667Val)
|
|
|
NM_001291303.3(FAT4):c.14000T>C (p.Met4667Thr)
|
|
|
NM_001291303.3(FAT4):c.14004C>G (p.Pro4668=)
|
rs769270880
|
|
NM_001291303.3(FAT4):c.14004C>T (p.Pro4668=)
|
|
|
NM_001291303.3(FAT4):c.14032C>T (p.Pro4678Ser)
|
|
|
NM_001291303.3(FAT4):c.14037A>G (p.Ser4679=)
|
rs2126097466
|
|
NM_001291303.3(FAT4):c.14041G>C (p.Gly4681Arg)
|
|
|
NM_001291303.3(FAT4):c.14042G>A (p.Gly4681Asp)
|
|
|
NM_001291303.3(FAT4):c.14057C>T (p.Thr4686Ile)
|
|
|
NM_001291303.3(FAT4):c.14069G>A (p.Ser4690Asn)
|
|
|
NM_001291303.3(FAT4):c.14073C>T (p.His4691=)
|
|
|
NM_001291303.3(FAT4):c.14086A>G (p.Thr4696Ala)
|
|
|
NM_001291303.3(FAT4):c.14088T>C (p.Thr4696=)
|
rs2126097563
|
|
NM_001291303.3(FAT4):c.14093A>G (p.Asn4698Ser)
|
rs1314487913
|
|
NM_001291303.3(FAT4):c.140A>G (p.Gln47Arg)
|
|
|
NM_001291303.3(FAT4):c.14109C>G (p.His4703Gln)
|
rs1409640096
|
|
NM_001291303.3(FAT4):c.14109C>T (p.His4703=)
|
rs1409640096
|
|
NM_001291303.3(FAT4):c.1412A>G (p.His471Arg)
|
|
|
NM_001291303.3(FAT4):c.14133T>C (p.Ser4711=)
|
|
|
NM_001291303.3(FAT4):c.14144A>G (p.Tyr4715Cys)
|
|
|
NM_001291303.3(FAT4):c.14145T>C (p.Tyr4715=)
|
|
|
NM_001291303.3(FAT4):c.14157A>G (p.Pro4719=)
|
|
|
NM_001291303.3(FAT4):c.14162G>A (p.Arg4721Lys)
|
|
|
NM_001291303.3(FAT4):c.14166A>G (p.Glu4722=)
|
|
|
NM_001291303.3(FAT4):c.14167T>A (p.Leu4723Met)
|
rs951647883
|
|
NM_001291303.3(FAT4):c.14175T>A (p.Leu4725=)
|
rs2126097738
|
|
NM_001291303.3(FAT4):c.14181A>T (p.Ile4727=)
|
|
|
NM_001291303.3(FAT4):c.14185G>A (p.Asp4729Asn)
|
|
|
NM_001291303.3(FAT4):c.14202A>G (p.Glu4734=)
|
rs1177710781
|
|
NM_001291303.3(FAT4):c.1421T>G (p.Val474Gly)
|
|
|
NM_001291303.3(FAT4):c.14241T>C (p.Tyr4747=)
|
|
|
NM_001291303.3(FAT4):c.14245A>G (p.Thr4749Ala)
|
|
|
NM_001291303.3(FAT4):c.14281A>G (p.Met4761Val)
|
|
|
NM_001291303.3(FAT4):c.14282T>C (p.Met4761Thr)
|
|
|
NM_001291303.3(FAT4):c.14291A>G (p.His4764Arg)
|
|
|
NM_001291303.3(FAT4):c.14307G>A (p.Gly4769=)
|
|
|
NM_001291303.3(FAT4):c.14312G>A (p.Arg4771His)
|
|
|
NM_001291303.3(FAT4):c.14324C>T (p.Pro4775Leu)
|
|
|
NM_001291303.3(FAT4):c.14325G>T (p.Pro4775=)
|
|
|
NM_001291303.3(FAT4):c.14328T>C (p.Ile4776=)
|
|
|
NM_001291303.3(FAT4):c.14328T>G (p.Ile4776Met)
|
|
|
NM_001291303.3(FAT4):c.1435G>A (p.Val479Met)
|
|
|
NM_001291303.3(FAT4):c.14368T>C (p.Ser4790Pro)
|
rs1490011143
|
|
NM_001291303.3(FAT4):c.14371A>G (p.Ile4791Val)
|
|
|
NM_001291303.3(FAT4):c.14371A>T (p.Ile4791Phe)
|
rs751534442
|
|
NM_001291303.3(FAT4):c.14383G>A (p.Glu4795Lys)
|
|
|
NM_001291303.3(FAT4):c.14386_14387del (p.Arg4796fs)
|
rs2126098060
|
|
NM_001291303.3(FAT4):c.14389C>T (p.Leu4797Phe)
|
rs267600018
|
|
NM_001291303.3(FAT4):c.14394C>T (p.Asn4798=)
|
|
|
NM_001291303.3(FAT4):c.14406T>C (p.Pro4802=)
|
rs2126098109
|
|
NM_001291303.3(FAT4):c.14410A>G (p.Asn4804Asp)
|
|
|
NM_001291303.3(FAT4):c.1443A>G (p.Arg481=)
|
|
|
NM_001291303.3(FAT4):c.14462G>A (p.Cys4821Tyr)
|
|
|
NM_001291303.3(FAT4):c.14462G>T (p.Cys4821Phe)
|
rs889999062
|
|
NM_001291303.3(FAT4):c.14463C>T (p.Cys4821=)
|
rs2126098198
|
|
NM_001291303.3(FAT4):c.14465G>T (p.Arg4822Ile)
|
|
|
NM_001291303.3(FAT4):c.14466A>T (p.Arg4822Ser)
|
|
|
NM_001291303.3(FAT4):c.14472A>G (p.Pro4824=)
|
|
|
NM_001291303.3(FAT4):c.14478T>C (p.Ser4826=)
|
|
|
NM_001291303.3(FAT4):c.14485A>G (p.Arg4829Gly)
|
|
|
NM_001291303.3(FAT4):c.14488A>G (p.Asn4830Asp)
|
|
|
NM_001291303.3(FAT4):c.1448A>G (p.Asn483Ser)
|
rs2125940248
|
|
NM_001291303.3(FAT4):c.14493A>G (p.Pro4831=)
|
|
|
NM_001291303.3(FAT4):c.14496G>A (p.Ala4832=)
|
|
|
NM_001291303.3(FAT4):c.14496G>T (p.Ala4832=)
|
|
|
NM_001291303.3(FAT4):c.1449C>T (p.Asn483=)
|
|
|
NM_001291303.3(FAT4):c.14516A>T (p.Glu4839Val)
|
|
|
NM_001291303.3(FAT4):c.1451T>A (p.Leu484Gln)
|
|
|
NM_001291303.3(FAT4):c.1452G>A (p.Leu484=)
|
|
|
NM_001291303.3(FAT4):c.14541T>C (p.His4847=)
|
|
|
NM_001291303.3(FAT4):c.14547_14550del (p.Phe4850fs)
|
|
|
NM_001291303.3(FAT4):c.14563A>G (p.Met4855Val)
|
rs1560640910
|
|
NM_001291303.3(FAT4):c.14583G>A (p.Lys4861=)
|
|
|
NM_001291303.3(FAT4):c.14590G>A (p.Val4864Ile)
|
|
|
NM_001291303.3(FAT4):c.14592A>G (p.Val4864=)
|
|
|
NM_001291303.3(FAT4):c.14592A>T (p.Val4864=)
|
|
|
NM_001291303.3(FAT4):c.14597C>T (p.Thr4866Ile)
|
|
|
NM_001291303.3(FAT4):c.1459G>A (p.Glu487Lys)
|
|
|
NM_001291303.3(FAT4):c.14604_14605delinsGC (p.Met4869Leu)
|
rs2126098406
|
|
NM_001291303.3(FAT4):c.14616A>G (p.Leu4872=)
|
|
|
NM_001291303.3(FAT4):c.1462G>A (p.Ala488Thr)
|
|
|
NM_001291303.3(FAT4):c.14634T>C (p.Ser4878=)
|
|
|
NM_001291303.3(FAT4):c.14644G>A (p.Asp4882Asn)
|
|
|
NM_001291303.3(FAT4):c.1464G>A (p.Ala488=)
|
|
|
NM_001291303.3(FAT4):c.14652T>C (p.Asp4884=)
|
|
|
NM_001291303.3(FAT4):c.14667A>G (p.Arg4889=)
|
|
|
NM_001291303.3(FAT4):c.14667A>T (p.Arg4889Ser)
|
|
|
NM_001291303.3(FAT4):c.14677C>G (p.Arg4893Gly)
|
rs765997899
|
|
NM_001291303.3(FAT4):c.1467T>A (p.Pro489=)
|
|
|
NM_001291303.3(FAT4):c.14684A>G (p.Tyr4895Cys)
|
rs1727640929
|
|
NM_001291303.3(FAT4):c.14692C>T (p.Arg4898Cys)
|
|
|
NM_001291303.3(FAT4):c.14704G>A (p.Gly4902Arg)
|
rs2126098617
|
|
NM_001291303.3(FAT4):c.14708G>C (p.Gly4903Ala)
|
|
|
NM_001291303.3(FAT4):c.14708_14710delinsCAGCACCCAGG (p.Gly4903fs)
|
|
|
NM_001291303.3(FAT4):c.14719A>G (p.Thr4907Ala)
|
rs769212397
|
|
NM_001291303.3(FAT4):c.14725G>A (p.Ala4909Thr)
|
|
|
NM_001291303.3(FAT4):c.14743G>A (p.Ala4915Thr)
|
rs1363330131
|
|
NM_001291303.3(FAT4):c.14756T>C (p.Leu4919Pro)
|
|
|
NM_001291303.3(FAT4):c.14762T>G (p.Met4921Arg)
|
|
|
NM_001291303.3(FAT4):c.14766G>T (p.Lys4922Asn)
|
|
|
NM_001291303.3(FAT4):c.14786C>T (p.Thr4929Ile)
|
|
|
NM_001291303.3(FAT4):c.14794T>G (p.Trp4932Gly)
|
|
|
NM_001291303.3(FAT4):c.1479T>C (p.Tyr493=)
|
|
|
NM_001291303.3(FAT4):c.147C>T (p.Phe49=)
|
|
|
NM_001291303.3(FAT4):c.14802C>A (p.Asn4934Lys)
|
|
|
NM_001291303.3(FAT4):c.14803C>A (p.Leu4935Ile)
|
|
|
NM_001291303.3(FAT4):c.14804T>C (p.Leu4935Pro)
|
|
|
NM_001291303.3(FAT4):c.14806T>C (p.Leu4936=)
|
rs1727650276
|
|
NM_001291303.3(FAT4):c.14807T>C (p.Leu4936Ser)
|
rs373636090
|
|
NM_001291303.3(FAT4):c.14807T>G (p.Leu4936Trp)
|
|
|
NM_001291303.3(FAT4):c.14815G>C (p.Gly4939Arg)
|
rs778778303
|
|
NM_001291303.3(FAT4):c.14815G>T (p.Gly4939Cys)
|
|
|
NM_001291303.3(FAT4):c.14816G>A (p.Gly4939Asp)
|
|
|
NM_001291303.3(FAT4):c.14816G>T (p.Gly4939Val)
|
rs2126098865
|
|
NM_001291303.3(FAT4):c.1482G>T (p.Val494=)
|
|
|
NM_001291303.3(FAT4):c.14835T>C (p.Tyr4945=)
|
|
|
NM_001291303.3(FAT4):c.14837T>C (p.Val4946Ala)
|
rs1727651908
|
|
NM_001291303.3(FAT4):c.14841T>A (p.Asp4947Glu)
|
rs768693221
|
|
NM_001291303.3(FAT4):c.14841T>C (p.Asp4947=)
|
|
|
NM_001291303.3(FAT4):c.14842G>A (p.Val4948Ile)
|
rs748711864
|
|
NM_001291303.3(FAT4):c.14860T>C (p.Ser4954Pro)
|
|
|
NM_001291303.3(FAT4):c.14864T>C (p.Leu4955Pro)
|
rs2126098929
|
|
NM_001291303.3(FAT4):c.14874dup (p.Ala4959fs)
|
|
|
NM_001291303.3(FAT4):c.14886dup (p.Glu4963Ter)
|
|
|
NM_001291303.3(FAT4):c.14892A>C (p.Glu4964Asp)
|
|
|
NM_001291303.3(FAT4):c.14906C>A (p.Thr4969Lys)
|
|
|
NM_001291303.3(FAT4):c.14906C>T (p.Thr4969Ile)
|
rs763678476
|
|
NM_001291303.3(FAT4):c.14936C>A (p.Ala4979Glu)
|
|
|
NM_001291303.3(FAT4):c.14945A>G (p.Tyr4982Cys)
|
|
|
NM_001291303.3(FAT4):c.14945_14946del (p.Tyr4982fs)
|
|
|
NM_001291303.3(FAT4):c.1497C>T (p.Ala499=)
|
rs760487098
|
|
NM_001291303.3(FAT4):c.1516C>G (p.Leu506Val)
|
|
|
NM_001291303.3(FAT4):c.151G>C (p.Val51Leu)
|
|
|
NM_001291303.3(FAT4):c.1525A>C (p.Asn509His)
|
rs1730707960
|
|
NM_001291303.3(FAT4):c.152T>G (p.Val51Gly)
|
rs1730603395
|
|
NM_001291303.3(FAT4):c.1545C>T (p.Val515=)
|
|
|
NM_001291303.3(FAT4):c.1548T>C (p.Ser516=)
|
rs2125940386
|
|
NM_001291303.3(FAT4):c.1551C>G (p.Gly517=)
|
|
|
NM_001291303.3(FAT4):c.1553A>G (p.Asn518Ser)
|
rs1730710235
|
|
NM_001291303.3(FAT4):c.155T>C (p.Leu52Pro)
|
|
|
NM_001291303.3(FAT4):c.1569C>G (p.Phe523Leu)
|
rs2125940402
|
|
NM_001291303.3(FAT4):c.1584T>A (p.His528Gln)
|
|
|
NM_001291303.3(FAT4):c.1584T>C (p.His528=)
|
|
|
NM_001291303.3(FAT4):c.1588G>A (p.Gly530Ser)
|
|
|
NM_001291303.3(FAT4):c.1593C>G (p.Leu531=)
|
|
|
NM_001291303.3(FAT4):c.1599del (p.Thr534fs)
|
|
|
NM_001291303.3(FAT4):c.1617C>T (p.Gly539=)
|
|
|
NM_001291303.3(FAT4):c.1619T>G (p.Leu540Arg)
|
rs1172348894
|
|
NM_001291303.3(FAT4):c.1624C>T (p.Arg542Cys)
|
|
|
NM_001291303.3(FAT4):c.1634C>T (p.Ala545Val)
|
|
|
NM_001291303.3(FAT4):c.1636T>C (p.Ser546Pro)
|
rs1371537193
|
|
NM_001291303.3(FAT4):c.1637C>T (p.Ser546Phe)
|
|
|
NM_001291303.3(FAT4):c.1648C>T (p.Leu550=)
|
|
|
NM_001291303.3(FAT4):c.164A>G (p.Gln55Arg)
|
|
|
NM_001291303.3(FAT4):c.1654A>G (p.Ile552Val)
|
|
|
NM_001291303.3(FAT4):c.1660G>A (p.Ala554Thr)
|
|
|
NM_001291303.3(FAT4):c.1662C>T (p.Ala554=)
|
|
|
NM_001291303.3(FAT4):c.1687G>T (p.Val563Leu)
|
rs377621635
|
|
NM_001291303.3(FAT4):c.169C>G (p.Pro57Ala)
|
rs1730604770
|
|
NM_001291303.3(FAT4):c.1705G>A (p.Val569Ile)
|
rs1730724185
|
|
NM_001291303.3(FAT4):c.1719A>G (p.Leu573=)
|
rs2125940631
|
|
NM_001291303.3(FAT4):c.1720G>C (p.Asp574His)
|
|
|
NM_001291303.3(FAT4):c.172G>A (p.Gly58Ser)
|
|
|
NM_001291303.3(FAT4):c.1738C>G (p.Pro580Ala)
|
rs1220275998
|
|
NM_001291303.3(FAT4):c.1739C>T (p.Pro580Leu)
|
|
|
NM_001291303.3(FAT4):c.1740A>G (p.Pro580=)
|
|
|
NM_001291303.3(FAT4):c.1750C>A (p.Gln584Lys)
|
|
|
NM_001291303.3(FAT4):c.1752G>A (p.Gln584=)
|
|
|
NM_001291303.3(FAT4):c.1754C>T (p.Pro585Leu)
|
|
|
NM_001291303.3(FAT4):c.1758A>G (p.Glu586=)
|
|
|
NM_001291303.3(FAT4):c.1770G>T (p.Val590=)
|
|
|
NM_001291303.3(FAT4):c.1778T>C (p.Val593Ala)
|
|
|
NM_001291303.3(FAT4):c.1787C>T (p.Ala596Val)
|
rs1730729533
|
|
NM_001291303.3(FAT4):c.1793C>A (p.Thr598Lys)
|
|
|
NM_001291303.3(FAT4):c.1794A>G (p.Thr598=)
|
rs1578514072
|
|
NM_001291303.3(FAT4):c.1796G>A (p.Gly599Glu)
|
|
|
NM_001291303.3(FAT4):c.1810A>T (p.Met604Leu)
|
|
|
NM_001291303.3(FAT4):c.1817G>C (p.Arg606Thr)
|
|
|
NM_001291303.3(FAT4):c.1827C>A (p.Asp609Glu)
|
rs370300509
|
|
NM_001291303.3(FAT4):c.1827C>T (p.Asp609=)
|
rs370300509
|
|
NM_001291303.3(FAT4):c.1828G>A (p.Gly610Arg)
|
rs374235705
|
|
NM_001291303.3(FAT4):c.1848A>T (p.Gly616=)
|
|
|
NM_001291303.3(FAT4):c.1851A>G (p.Thr617=)
|
|
|
NM_001291303.3(FAT4):c.1866A>G (p.Leu622=)
|
|
|
NM_001291303.3(FAT4):c.1884C>T (p.Asp628=)
|
|
|
NM_001291303.3(FAT4):c.1886G>A (p.Arg629Gln)
|
|
|
NM_001291303.3(FAT4):c.1890G>T (p.Arg630Ser)
|
rs1730738135
|
|
NM_001291303.3(FAT4):c.1898G>A (p.Arg633His)
|
rs370926669
|
|
NM_001291303.3(FAT4):c.1898G>T (p.Arg633Leu)
|
rs370926669
|
|
NM_001291303.3(FAT4):c.1902G>C (p.Leu634=)
|
|
|
NM_001291303.3(FAT4):c.1903G>A (p.Asp635Asn)
|
|
|
NM_001291303.3(FAT4):c.1903G>T (p.Asp635Tyr)
|
rs374308807
|
|
NM_001291303.3(FAT4):c.1929T>C (p.Thr643=)
|
rs2125940937
|
|
NM_001291303.3(FAT4):c.1934C>T (p.Ser645Phe)
|
rs1730741084
|
|
NM_001291303.3(FAT4):c.1935C>T (p.Ser645=)
|
rs2125940949
|
|
NM_001291303.3(FAT4):c.1962C>T (p.Phe654=)
|
|
|
NM_001291303.3(FAT4):c.1966T>C (p.Ser656Pro)
|
rs1730743959
|
|
NM_001291303.3(FAT4):c.1974G>A (p.Leu658=)
|
|
|
NM_001291303.3(FAT4):c.1978C>T (p.Leu660=)
|
|
|
NM_001291303.3(FAT4):c.198G>C (p.Thr66=)
|
|
|
NM_001291303.3(FAT4):c.1990C>T (p.Leu664=)
|
|
|
NM_001291303.3(FAT4):c.2011T>C (p.Ser671Pro)
|
|
|
NM_001291303.3(FAT4):c.2021G>T (p.Arg674Leu)
|
rs759309740
|
|
NM_001291303.3(FAT4):c.2033G>A (p.Ser678Asn)
|
|
|
NM_001291303.3(FAT4):c.2044A>G (p.Ile682Val)
|
|
|
NM_001291303.3(FAT4):c.2072C>T (p.Pro691Leu)
|
|
|
NM_001291303.3(FAT4):c.2073G>A (p.Pro691=)
|
|
|
NM_001291303.3(FAT4):c.2074G>C (p.Val692Leu)
|
|
|
NM_001291303.3(FAT4):c.2082C>T (p.Tyr694=)
|
|
|
NM_001291303.3(FAT4):c.2103T>C (p.Asn701=)
|
|
|
NM_001291303.3(FAT4):c.2118C>T (p.Ser706=)
|
|
|
NM_001291303.3(FAT4):c.2124C>T (p.Ile708=)
|
|
|
NM_001291303.3(FAT4):c.2126C>T (p.Thr709Ile)
|
|
|
NM_001291303.3(FAT4):c.213C>T (p.Thr71=)
|
|
|
NM_001291303.3(FAT4):c.2148A>C (p.Pro716=)
|
rs1730755602
|
|
NM_001291303.3(FAT4):c.2170G>C (p.Val724Leu)
|
|
|
NM_001291303.3(FAT4):c.2178T>C (p.Tyr726=)
|
|
|
NM_001291303.3(FAT4):c.2182A>G (p.Ile728Val)
|
|
|
NM_001291303.3(FAT4):c.2200T>C (p.Ser734Pro)
|
rs2125941329
|
|
NM_001291303.3(FAT4):c.2214C>A (p.Val738=)
|
|
|
NM_001291303.3(FAT4):c.2216A>G (p.Asn739Ser)
|
rs200512777
|
|
NM_001291303.3(FAT4):c.2216A>T (p.Asn739Ile)
|
rs200512777
|
|
NM_001291303.3(FAT4):c.222C>T (p.Leu74=)
|
|
|
NM_001291303.3(FAT4):c.2239A>G (p.Thr747Ala)
|
|
|
NM_001291303.3(FAT4):c.225C>T (p.Ser75=)
|
|
|
NM_001291303.3(FAT4):c.2277T>C (p.Tyr759=)
|
|
|
NM_001291303.3(FAT4):c.2286A>G (p.Gln762=)
|
rs771276464
|
|
NM_001291303.3(FAT4):c.2309A>T (p.Asn770Ile)
|
|
|
NM_001291303.3(FAT4):c.2316A>C (p.Gln772His)
|
rs187427286
|
|
NM_001291303.3(FAT4):c.2316A>G (p.Gln772=)
|
rs187427286
|
|
NM_001291303.3(FAT4):c.2338A>T (p.Thr780Ser)
|
|
|
NM_001291303.3(FAT4):c.234C>A (p.His78Gln)
|
|
|
NM_001291303.3(FAT4):c.235G>T (p.Ala79Ser)
|
|
|
NM_001291303.3(FAT4):c.2361A>C (p.Gln787His)
|
rs2125941586
|
|
NM_001291303.3(FAT4):c.237C>T (p.Ala79=)
|
|
|
NM_001291303.3(FAT4):c.2415C>T (p.Asn805=)
|
|
|
NM_001291303.3(FAT4):c.2416G>A (p.Val806Met)
|
|
|
NM_001291303.3(FAT4):c.2421G>T (p.Ala807=)
|
|
|
NM_001291303.3(FAT4):c.2424G>T (p.Leu808=)
|
|
|
NM_001291303.3(FAT4):c.2449G>C (p.Ala817Pro)
|
rs1213814030
|
|
NM_001291303.3(FAT4):c.24T>C (p.Ala8=)
|
|
|
NM_001291303.3(FAT4):c.2508A>G (p.Lys836=)
|
|
|
NM_001291303.3(FAT4):c.2514G>C (p.Met838Ile)
|
|
|
NM_001291303.3(FAT4):c.2527C>T (p.Gln843Ter)
|
rs1064793943
|
|
NM_001291303.3(FAT4):c.2535T>A (p.Thr845=)
|
|
|
NM_001291303.3(FAT4):c.253A>G (p.Ser85Gly)
|
rs1277663930
|
|
NM_001291303.3(FAT4):c.2555A>G (p.Asn852Ser)
|
rs2125941924
|
|
NM_001291303.3(FAT4):c.2574G>A (p.Glu858=)
|
|
|
NM_001291303.3(FAT4):c.2604C>T (p.Ala868=)
|
|
|
NM_001291303.3(FAT4):c.2608G>A (p.Gly870Arg)
|
rs2125941989
|
|
NM_001291303.3(FAT4):c.2610G>A (p.Gly870=)
|
|
|
NM_001291303.3(FAT4):c.2611G>T (p.Gly871Cys)
|
|
|
NM_001291303.3(FAT4):c.2614A>G (p.Thr872Ala)
|
|
|
NM_001291303.3(FAT4):c.261C>T (p.Thr87=)
|
|
|
NM_001291303.3(FAT4):c.262G>A (p.Gly88Arg)
|
|
|
NM_001291303.3(FAT4):c.2630C>G (p.Thr877Ser)
|
|
|
NM_001291303.3(FAT4):c.2632A>G (p.Met878Val)
|
rs773388017
|
|
NM_001291303.3(FAT4):c.2632_2633del (p.Met878fs)
|
|
|
NM_001291303.3(FAT4):c.2635G>A (p.Val879Ile)
|
|
|
NM_001291303.3(FAT4):c.2694G>A (p.Glu898=)
|
|
|
NM_001291303.3(FAT4):c.2697T>C (p.Ser899=)
|
|
|
NM_001291303.3(FAT4):c.2702A>G (p.Asn901Ser)
|
rs2125942162
|
|
NM_001291303.3(FAT4):c.2704G>A (p.Val902Met)
|
rs2125942165
|
|
NM_001291303.3(FAT4):c.2705TGG[1] (p.Val903del)
|
rs541157165
|
|
NM_001291303.3(FAT4):c.2706G>A (p.Val902=)
|
|
|
NM_001291303.3(FAT4):c.270G>A (p.Leu90=)
|
rs2125938508
|
|
NM_001291303.3(FAT4):c.2774A>G (p.Asn925Ser)
|
|
|
NM_001291303.3(FAT4):c.2787C>T (p.Leu929=)
|
rs1730806684
|
|
NM_001291303.3(FAT4):c.2791A>G (p.Ser931Gly)
|
rs1730806878
|
|
NM_001291303.3(FAT4):c.2804A>T (p.Asn935Ile)
|
|
|
NM_001291303.3(FAT4):c.2814C>A (p.Asn938Lys)
|
|
|
NM_001291303.3(FAT4):c.2821G>T (p.Ala941Ser)
|
rs1730808695
|
|
NM_001291303.3(FAT4):c.2823T>C (p.Ala941=)
|
|
|
NM_001291303.3(FAT4):c.2827A>C (p.Asn943His)
|
|
|
NM_001291303.3(FAT4):c.2861C>A (p.Pro954His)
|
|
|
NM_001291303.3(FAT4):c.2866G>C (p.Asp956His)
|
|
|
NM_001291303.3(FAT4):c.2883C>T (p.Ser961=)
|
rs756899944
|
|
NM_001291303.3(FAT4):c.2899T>C (p.Leu967=)
|
|
|
NM_001291303.3(FAT4):c.2903C>T (p.Ala968Val)
|
rs1390864938
|
|
NM_001291303.3(FAT4):c.2904A>T (p.Ala968=)
|
|
|
NM_001291303.3(FAT4):c.2905T>A (p.Ser969Thr)
|
|
|
NM_001291303.3(FAT4):c.2921del (p.Pro974fs)
|
rs2125942518
|
|
NM_001291303.3(FAT4):c.2928C>A (p.Leu976=)
|
|
|
NM_001291303.3(FAT4):c.2947A>G (p.Thr983Ala)
|
|
|
NM_001291303.3(FAT4):c.2947A>T (p.Thr983Ser)
|
|
|
NM_001291303.3(FAT4):c.2949A>C (p.Thr983=)
|
|
|
NM_001291303.3(FAT4):c.2956G>A (p.Val986Ile)
|
|
|
NM_001291303.3(FAT4):c.2957T>A (p.Val986Asp)
|
|
|
NM_001291303.3(FAT4):c.2965G>A (p.Val989Ile)
|
|
|
NM_001291303.3(FAT4):c.2967A>G (p.Val989=)
|
|
|
NM_001291303.3(FAT4):c.2978C>T (p.Ser993Leu)
|
|
|
NM_001291303.3(FAT4):c.2979A>C (p.Ser993=)
|
rs2125942607
|
|
NM_001291303.3(FAT4):c.2981C>T (p.Pro994Leu)
|
|
|
NM_001291303.3(FAT4):c.2989G>C (p.Asp997His)
|
|
|
NM_001291303.3(FAT4):c.300C>G (p.Ser100Arg)
|
|
|
NM_001291303.3(FAT4):c.3012C>A (p.Thr1004=)
|
|
|
NM_001291303.3(FAT4):c.3022_3023delinsAT (p.Ser1008Ile)
|
|
|
NM_001291303.3(FAT4):c.3028C>T (p.Pro1010Ser)
|
rs771044290
|
|
NM_001291303.3(FAT4):c.3040C>T (p.Arg1014Ter)
|
|
|
NM_001291303.3(FAT4):c.3055C>G (p.Gln1019Glu)
|
rs761032436
|
|
NM_001291303.3(FAT4):c.3057A>G (p.Gln1019=)
|
|
|
NM_001291303.3(FAT4):c.3063T>A (p.Ser1021=)
|
|
|
NM_001291303.3(FAT4):c.3065A>G (p.Asp1022Gly)
|
rs372060616
|
|
NM_001291303.3(FAT4):c.3119C>G (p.Thr1040Arg)
|
|
|
NM_001291303.3(FAT4):c.3119C>T (p.Thr1040Ile)
|
|
|
NM_001291303.3(FAT4):c.3122G>A (p.Gly1041Glu)
|
rs2125942835
|
|
NM_001291303.3(FAT4):c.3133G>A (p.Gly1045Ser)
|
rs2125942862
|
|
NM_001291303.3(FAT4):c.3135C>T (p.Gly1045=)
|
|
|
NM_001291303.3(FAT4):c.3136A>G (p.Ile1046Val)
|
|
|
NM_001291303.3(FAT4):c.3138A>G (p.Ile1046Met)
|
|
|
NM_001291303.3(FAT4):c.3150T>C (p.Gly1050=)
|
|
|
NM_001291303.3(FAT4):c.3154T>C (p.Leu1052=)
|
|
|
NM_001291303.3(FAT4):c.3167G>A (p.Ser1056Asn)
|
rs1390761515
|
|
NM_001291303.3(FAT4):c.316A>T (p.Ile106Phe)
|
rs746331785
|
|
NM_001291303.3(FAT4):c.3178C>T (p.Arg1060Cys)
|
|
|
NM_001291303.3(FAT4):c.3196T>C (p.Tyr1066His)
|
rs374993866
|
|
NM_001291303.3(FAT4):c.3198T>C (p.Tyr1066=)
|
|
|
NM_001291303.3(FAT4):c.3228A>G (p.Ala1076=)
|
rs777609137
|
|
NM_001291303.3(FAT4):c.322C>T (p.Leu108=)
|
|
|
NM_001291303.3(FAT4):c.3231G>A (p.Val1077=)
|
|
|
NM_001291303.3(FAT4):c.3270A>G (p.Leu1090=)
|
|
|
NM_001291303.3(FAT4):c.3288C>A (p.Asn1096Lys)
|
|
|
NM_001291303.3(FAT4):c.3288C>T (p.Asn1096=)
|
|
|
NM_001291303.3(FAT4):c.3327C>T (p.Phe1109=)
|
|
|
NM_001291303.3(FAT4):c.333T>C (p.Leu111=)
|
|
|
NM_001291303.3(FAT4):c.3346G>T (p.Gly1116Trp)
|
rs2125943177
|
|
NM_001291303.3(FAT4):c.3364G>C (p.Val1122Leu)
|
rs995967911
|
|
NM_001291303.3(FAT4):c.3368G>T (p.Ser1123Ile)
|
|
|
NM_001291303.3(FAT4):c.3388G>A (p.Gly1130Arg)
|
|
|
NM_001291303.3(FAT4):c.3408G>A (p.Arg1136=)
|
|
|
NM_001291303.3(FAT4):c.3408G>T (p.Arg1136Ser)
|
|
|
NM_001291303.3(FAT4):c.3409T>C (p.Tyr1137His)
|
|
|
NM_001291303.3(FAT4):c.3458G>C (p.Gly1153Ala)
|
rs2125943347
|
|
NM_001291303.3(FAT4):c.3473C>T (p.Thr1158Ile)
|
|
|
NM_001291303.3(FAT4):c.3483T>G (p.Phe1161Leu)
|
|
|
NM_001291303.3(FAT4):c.3492G>A (p.Glu1164=)
|
|
|
NM_001291303.3(FAT4):c.3506G>A (p.Arg1169Gln)
|
|
|
NM_001291303.3(FAT4):c.3507G>A (p.Arg1169=)
|
|
|
NM_001291303.3(FAT4):c.350A>T (p.Tyr117Phe)
|
|
|
NM_001291303.3(FAT4):c.3515C>T (p.Thr1172Ile)
|
rs535333070
|
|
NM_001291303.3(FAT4):c.351C>T (p.Tyr117=)
|
|
|
NM_001291303.3(FAT4):c.3525T>A (p.Phe1175Leu)
|
rs2125943496
|
|
NM_001291303.3(FAT4):c.3537C>G (p.Val1179=)
|
|
|
NM_001291303.3(FAT4):c.3538A>G (p.Ile1180Val)
|
|
|
NM_001291303.3(FAT4):c.3555G>T (p.Gly1185=)
|
|
|
NM_001291303.3(FAT4):c.3564G>A (p.Gln1188=)
|
|
|
NM_001291303.3(FAT4):c.3577C>G (p.Gln1193Glu)
|
|
|
NM_001291303.3(FAT4):c.3580G>A (p.Ala1194Thr)
|
|
|
NM_001291303.3(FAT4):c.3591T>A (p.His1197Gln)
|
|
|
NM_001291303.3(FAT4):c.3614A>T (p.Asp1205Val)
|
rs2125943625
|
|
NM_001291303.3(FAT4):c.3617A>G (p.Asn1206Ser)
|
|
|
NM_001291303.3(FAT4):c.3633A>G (p.Leu1211=)
|
|
|
NM_001291303.3(FAT4):c.3641T>A (p.Phe1214Tyr)
|
rs372590258
|
|
NM_001291303.3(FAT4):c.3642T>C (p.Phe1214=)
|
|
|
NM_001291303.3(FAT4):c.3647A>G (p.Gln1216Arg)
|
|
|
NM_001291303.3(FAT4):c.3648A>G (p.Gln1216=)
|
|
|
NM_001291303.3(FAT4):c.3664T>C (p.Ser1222Pro)
|
rs2125943712
|
|
NM_001291303.3(FAT4):c.3668C>T (p.Ala1223Val)
|
|
|
NM_001291303.3(FAT4):c.3670G>A (p.Ala1224Thr)
|
|
|
NM_001291303.3(FAT4):c.3676C>A (p.Leu1226Met)
|
|
|
NM_001291303.3(FAT4):c.367G>C (p.Val123Leu)
|
|
|
NM_001291303.3(FAT4):c.3680C>T (p.Thr1227Ile)
|
rs2125943745
|
|
NM_001291303.3(FAT4):c.3687G>A (p.Val1229=)
|
rs7657251
|
|
NM_001291303.3(FAT4):c.3697T>A (p.Ser1233Thr)
|
rs2125943792
|
|
NM_001291303.3(FAT4):c.3704C>T (p.Ser1235Leu)
|
|
|
NM_001291303.3(FAT4):c.3708T>A (p.Asp1236Glu)
|
rs1223564463
|
|
NM_001291303.3(FAT4):c.3714T>C (p.Asp1238=)
|
rs780746680
|
|
NM_001291303.3(FAT4):c.3726T>A (p.Asn1242Lys)
|
|
|
NM_001291303.3(FAT4):c.3726T>C (p.Asn1242=)
|
rs903106127
|
|
NM_001291303.3(FAT4):c.3726T>G (p.Asn1242Lys)
|
rs903106127
|
|
NM_001291303.3(FAT4):c.3737A>G (p.His1246Arg)
|
|
|
NM_001291303.3(FAT4):c.3740A>G (p.Tyr1247Cys)
|
|
|
NM_001291303.3(FAT4):c.3744T>C (p.Ser1248=)
|
|
|
NM_001291303.3(FAT4):c.377G>A (p.Arg126Gln)
|
|
|
NM_001291303.3(FAT4):c.3783C>T (p.Asp1261=)
|
|
|
NM_001291303.3(FAT4):c.3797A>G (p.Gln1266Arg)
|
rs2125943945
|
|
NM_001291303.3(FAT4):c.37T>C (p.Trp13Arg)
|
rs2125938137
|
|
NM_001291303.3(FAT4):c.3801A>G (p.Val1267=)
|
|
|
NM_001291303.3(FAT4):c.3808A>C (p.Ile1270Leu)
|
|
|
NM_001291303.3(FAT4):c.3809T>C (p.Ile1270Thr)
|
|
|
NM_001291303.3(FAT4):c.3810T>C (p.Ile1270=)
|
|
|
NM_001291303.3(FAT4):c.3813C>T (p.Gly1271=)
|
|
|
NM_001291303.3(FAT4):c.3818T>C (p.Leu1273Ser)
|
rs2125943983
|
|
NM_001291303.3(FAT4):c.3822C>T (p.Asp1274=)
|
|
|
NM_001291303.3(FAT4):c.382C>T (p.Leu128Phe)
|
|
|
NM_001291303.3(FAT4):c.3842A>G (p.Tyr1281Cys)
|
rs1317645126
|
|
NM_001291303.3(FAT4):c.3848T>C (p.Leu1283Pro)
|
|
|
NM_001291303.3(FAT4):c.3853A>T (p.Ile1285Phe)
|
|
|
NM_001291303.3(FAT4):c.3859G>A (p.Ala1287Thr)
|
|
|
NM_001291303.3(FAT4):c.386A>G (p.Asn129Ser)
|
rs754070949
|
|
NM_001291303.3(FAT4):c.3870A>G (p.Ser1290=)
|
|
|
NM_001291303.3(FAT4):c.3873G>T (p.Gly1291=)
|
|
|
NM_001291303.3(FAT4):c.3887A>G (p.Asn1296Ser)
|
|
|
NM_001291303.3(FAT4):c.3893C>T (p.Thr1298Met)
|
|
|
NM_001291303.3(FAT4):c.3894G>A (p.Thr1298=)
|
|
|
NM_001291303.3(FAT4):c.390C>G (p.Asp130Glu)
|
|
|
NM_001291303.3(FAT4):c.3918A>T (p.Leu1306Phe)
|
rs758711821
|
|
NM_001291303.3(FAT4):c.3922G>T (p.Glu1308Ter)
|
|
|
NM_001291303.3(FAT4):c.3926A>G (p.Asn1309Ser)
|
rs184971791
|
|
NM_001291303.3(FAT4):c.3929A>G (p.Asp1310Gly)
|
|
|
NM_001291303.3(FAT4):c.3930C>A (p.Asp1310Glu)
|
|
|
NM_001291303.3(FAT4):c.3936C>T (p.Thr1312=)
|
|
|
NM_001291303.3(FAT4):c.393C>T (p.Asn131=)
|
|
|
NM_001291303.3(FAT4):c.3986G>A (p.Arg1329Lys)
|
|
|
NM_001291303.3(FAT4):c.3999C>T (p.Leu1333=)
|
|
|
NM_001291303.3(FAT4):c.400G>T (p.Val134Phe)
|
rs1560751923
|
|
NM_001291303.3(FAT4):c.4015G>T (p.Ala1339Ser)
|
rs1466033768
|
|
NM_001291303.3(FAT4):c.4017A>C (p.Ala1339=)
|
|
|
NM_001291303.3(FAT4):c.4026C>T (p.Ser1342=)
|
|
|
NM_001291303.3(FAT4):c.4027G>A (p.Asp1343Asn)
|
|
|
NM_001291303.3(FAT4):c.4037A>G (p.Asp1346Gly)
|
|
|
NM_001291303.3(FAT4):c.4038C>A (p.Asp1346Glu)
|
rs1221303871
|
|
NM_001291303.3(FAT4):c.4040A>G (p.Asn1347Ser)
|
|
|
NM_001291303.3(FAT4):c.4050A>G (p.Leu1350=)
|
rs1730889782
|
|
NM_001291303.3(FAT4):c.4083A>G (p.Gly1361=)
|
|
|
NM_001291303.3(FAT4):c.4087T>G (p.Phe1363Val)
|
|
|
NM_001291303.3(FAT4):c.4101A>C (p.Pro1367=)
|
|
|
NM_001291303.3(FAT4):c.4110G>A (p.Gly1370=)
|
|
|
NM_001291303.3(FAT4):c.4114A>G (p.Ile1372Val)
|
|
|
NM_001291303.3(FAT4):c.4131A>G (p.Lys1377=)
|
|
|
NM_001291303.3(FAT4):c.4157A>G (p.Tyr1386Cys)
|
|
|
NM_001291303.3(FAT4):c.4162T>C (p.Leu1388=)
|
rs2125944598
|
|
NM_001291303.3(FAT4):c.4176A>G (p.Ala1392=)
|
|
|
NM_001291303.3(FAT4):c.417T>C (p.Ser139=)
|
|
|
NM_001291303.3(FAT4):c.418A>G (p.Ile140Val)
|
rs1730623781
|
|
NM_001291303.3(FAT4):c.4195C>A (p.Pro1399Thr)
|
rs1486226093
|
|
NM_001291303.3(FAT4):c.4207A>T (p.Thr1403Ser)
|
|
|
NM_001291303.3(FAT4):c.4209A>G (p.Thr1403=)
|
|
|
NM_001291303.3(FAT4):c.4210A>G (p.Met1404Val)
|
rs779982980
|
|
NM_001291303.3(FAT4):c.4219G>C (p.Val1407Leu)
|
rs114227532
|
|
NM_001291303.3(FAT4):c.4232G>A (p.Arg1411Lys)
|
|
|
NM_001291303.3(FAT4):c.4233G>A (p.Arg1411=)
|
|
|
NM_001291303.3(FAT4):c.4249C>A (p.Pro1417Thr)
|
|
|
NM_001291303.3(FAT4):c.428C>T (p.Thr143Ile)
|
|
|
NM_001291303.3(FAT4):c.42C>G (p.Leu14=)
|
|
|
NM_001291303.3(FAT4):c.42C>T (p.Leu14=)
|
|
|
NM_001291303.3(FAT4):c.4314T>C (p.Ser1438=)
|
rs1730904209
|
|
NM_001291303.3(FAT4):c.4332A>G (p.Ala1444=)
|
|
|
NM_001291303.3(FAT4):c.4374A>G (p.Thr1458=)
|
rs2125944971
|
|
NM_001291303.3(FAT4):c.4375A>G (p.Ile1459Val)
|
|
|
NM_001291303.3(FAT4):c.4398C>T (p.Gly1466=)
|
|
|
NM_001291303.3(FAT4):c.4411A>G (p.Ile1471Val)
|
rs1730909137
|
|
NM_001291303.3(FAT4):c.4413A>G (p.Ile1471Met)
|
rs2125945055
|
|
NM_001291303.3(FAT4):c.4432A>G (p.Ile1478Val)
|
rs200565115
|
|
NM_001291303.3(FAT4):c.4436A>G (p.Tyr1479Cys)
|
|
|
NM_001291303.3(FAT4):c.4456C>T (p.Arg1486Trp)
|
|
|
NM_001291303.3(FAT4):c.4457G>A (p.Arg1486Gln)
|
|
|
NM_001291303.3(FAT4):c.4467T>C (p.Ala1489=)
|
rs1479845446
|
|
NM_001291303.3(FAT4):c.4480_4481insG (p.Leu1494fs)
|
|
|
NM_001291303.3(FAT4):c.4481T>G (p.Leu1494Trp)
|
rs1327226148
|
|
NM_001291303.3(FAT4):c.4486G>A (p.Val1496Ile)
|
|
|
NM_001291303.3(FAT4):c.4496A>G (p.Asn1499Ser)
|
rs1241928722
|
|
NM_001291303.3(FAT4):c.4503A>G (p.Gln1501=)
|
|
|
NM_001291303.3(FAT4):c.4510C>T (p.Pro1504Ser)
|
|
|
NM_001291303.3(FAT4):c.4567A>G (p.Asn1523Asp)
|
|
|
NM_001291303.3(FAT4):c.4577T>C (p.Val1526Ala)
|
|
|
NM_001291303.3(FAT4):c.4593A>G (p.Ser1531=)
|
|
|
NM_001291303.3(FAT4):c.4604T>G (p.Leu1535Arg)
|
rs1359875187
|
|
NM_001291303.3(FAT4):c.4606G>T (p.Ala1536Ser)
|
rs765320042
|
|
NM_001291303.3(FAT4):c.4631G>A (p.Gly1544Asp)
|
|
|
NM_001291303.3(FAT4):c.4634C>T (p.Ser1545Phe)
|
|
|
NM_001291303.3(FAT4):c.4635C>T (p.Ser1545=)
|
|
|
NM_001291303.3(FAT4):c.4648A>G (p.Ile1550Val)
|
|
|
NM_001291303.3(FAT4):c.4649T>A (p.Ile1550Asn)
|
|
|
NM_001291303.3(FAT4):c.4650T>C (p.Ile1550=)
|
|
|
NM_001291303.3(FAT4):c.4662C>T (p.Asp1554=)
|
|
|
NM_001291303.3(FAT4):c.4664C>G (p.Pro1555Arg)
|
rs2125945465
|
|
NM_001291303.3(FAT4):c.4664C>T (p.Pro1555Leu)
|
|
|
NM_001291303.3(FAT4):c.4702A>G (p.Ile1568Val)
|
|
|
NM_001291303.3(FAT4):c.4711G>A (p.Asp1571Asn)
|
|
|
NM_001291303.3(FAT4):c.4715C>T (p.Thr1572Ile)
|
|
|
NM_001291303.3(FAT4):c.4721C>T (p.Thr1574Ile)
|
|
|
NM_001291303.3(FAT4):c.4725C>T (p.Phe1575=)
|
|
|
NM_001291303.3(FAT4):c.4749C>T (p.Asp1583=)
|
rs756478353
|
|
NM_001291303.3(FAT4):c.4754G>A (p.Arg1585Lys)
|
|
|
NM_001291303.3(FAT4):c.475G>T (p.Ala159Ser)
|
rs2125938762
|
|
NM_001291303.3(FAT4):c.4766C>A (p.Ala1589Glu)
|
|
|
NM_001291303.3(FAT4):c.4766C>T (p.Ala1589Val)
|
|
|
NM_001291303.3(FAT4):c.4767G>T (p.Ala1589=)
|
rs1333560320
|
|
NM_001291303.3(FAT4):c.4776T>C (p.Pro1592=)
|
|
|
NM_001291303.3(FAT4):c.4823C>T (p.Pro1608Leu)
|
rs2125945804
|
|
NM_001291303.3(FAT4):c.4837T>A (p.Ser1613Thr)
|
|
|
NM_001291303.3(FAT4):c.4848A>T (p.Glu1616Asp)
|
|
|
NM_001291303.3(FAT4):c.4852A>G (p.Thr1618Ala)
|
|
|
NM_001291303.3(FAT4):c.4869C>T (p.Gly1623=)
|
|
|
NM_001291303.3(FAT4):c.486G>A (p.Ser162=)
|
|
|
NM_001291303.3(FAT4):c.4930A>C (p.Ile1644Leu)
|
|
|
NM_001291303.3(FAT4):c.4944G>A (p.Val1648=)
|
|
|
NM_001291303.3(FAT4):c.4950A>G (p.Ser1650=)
|
|
|
NM_001291303.3(FAT4):c.4957G>A (p.Ala1653Thr)
|
|
|
NM_001291303.3(FAT4):c.4966C>A (p.Pro1656Thr)
|
rs1730936860
|
|
NM_001291303.3(FAT4):c.4980G>A (p.Glu1660=)
|
|
|
NM_001291303.3(FAT4):c.5000T>C (p.Ile1667Thr)
|
rs2125946113
|
|
NM_001291303.3(FAT4):c.501C>T (p.Asn167=)
|
|
|
NM_001291303.3(FAT4):c.5028T>C (p.Thr1676=)
|
|
|
NM_001291303.3(FAT4):c.502G>C (p.Gly168Arg)
|
|
|
NM_001291303.3(FAT4):c.5043T>A (p.Phe1681Leu)
|
|
|
NM_001291303.3(FAT4):c.5053C>G (p.Arg1685Gly)
|
rs760759561
|
|
NM_001291303.3(FAT4):c.5059A>G (p.Thr1687Ala)
|
|
|
NM_001291303.3(FAT4):c.5076C>T (p.Thr1692=)
|
|
|
NM_001291303.3(FAT4):c.5077G>A (p.Ala1693Thr)
|
|
|
NM_001291303.3(FAT4):c.5082C>T (p.Ala1694=)
|
|
|
NM_001291303.3(FAT4):c.5092C>T (p.Arg1698Trp)
|
|
|
NM_001291303.3(FAT4):c.5134A>T (p.Ile1712Leu)
|
|
|
NM_001291303.3(FAT4):c.5155C>G (p.Pro1719Ala)
|
|
|
NM_001291303.3(FAT4):c.5175+14A>G
|
|
|
NM_001291303.3(FAT4):c.5176-10T>C
|
|
|
NM_001291303.3(FAT4):c.5176-19G>T
|
|
|
NM_001291303.3(FAT4):c.5176-4G>T
|
|
|
NM_001291303.3(FAT4):c.5184A>G (p.Ile1728Met)
|
|
|
NM_001291303.3(FAT4):c.5198T>C (p.Ile1733Thr)
|
|
|
NM_001291303.3(FAT4):c.5225C>T (p.Thr1742Met)
|
|
|
NM_001291303.3(FAT4):c.522C>T (p.Tyr174=)
|
|
|
NM_001291303.3(FAT4):c.5230A>G (p.Met1744Val)
|
rs1472593009
|
|
NM_001291303.3(FAT4):c.5235G>A (p.Leu1745=)
|
|
|
NM_001291303.3(FAT4):c.523C>A (p.Arg175Ser)
|
|
|
NM_001291303.3(FAT4):c.5244G>A (p.Thr1748=)
|
|
|
NM_001291303.3(FAT4):c.5244G>C (p.Thr1748=)
|
|
|
NM_001291303.3(FAT4):c.5246T>C (p.Val1749Ala)
|
rs1734278499
|
|
NM_001291303.3(FAT4):c.5247A>G (p.Val1749=)
|
|
|
NM_001291303.3(FAT4):c.5256C>T (p.Asn1752=)
|
rs772614378
|
|
NM_001291303.3(FAT4):c.525C>T (p.Arg175=)
|
rs2125938821
|
|
NM_001291303.3(FAT4):c.5261del (p.Gly1754fs)
|
|
|
NM_001291303.3(FAT4):c.5271T>C (p.Ser1757=)
|
|
|
NM_001291303.3(FAT4):c.528C>G (p.Ile176Met)
|
|
|
NM_001291303.3(FAT4):c.5307+15T>A
|
|
|
NM_001291303.3(FAT4):c.5307+15T>G
|
|
|
NM_001291303.3(FAT4):c.5307+17T>A
|
|
|
NM_001291303.3(FAT4):c.5307+17T>C
|
|
|
NM_001291303.3(FAT4):c.5307+6T>A
|
rs910280782
|
|
NM_001291303.3(FAT4):c.5307+7C>G
|
|
|
NM_001291303.3(FAT4):c.5308-10C>G
|
|
|
NM_001291303.3(FAT4):c.5308-14G>C
|
|
|
NM_001291303.3(FAT4):c.5308-15G>A
|
|
|
NM_001291303.3(FAT4):c.5308-18C>T
|
|
|
NM_001291303.3(FAT4):c.5317G>T (p.Ala1773Ser)
|
rs750458935
|
|
NM_001291303.3(FAT4):c.5323G>A (p.Val1775Ile)
|
|
|
NM_001291303.3(FAT4):c.532C>A (p.Arg178Ser)
|
rs201952959
|
|
NM_001291303.3(FAT4):c.5331C>T (p.Tyr1777=)
|
|
|
NM_001291303.3(FAT4):c.5332A>G (p.Thr1778Ala)
|
|
|
NM_001291303.3(FAT4):c.5338A>T (p.Ile1780Phe)
|
|
|
NM_001291303.3(FAT4):c.5347G>A (p.Ala1783Thr)
|
rs571447839
|
|
NM_001291303.3(FAT4):c.5348C>T (p.Ala1783Val)
|
|
|
NM_001291303.3(FAT4):c.5355T>G (p.Asp1785Glu)
|
rs778606448
|
|
NM_001291303.3(FAT4):c.5370C>T (p.Asp1790=)
|
|
|
NM_001291303.3(FAT4):c.5389A>G (p.Ile1797Val)
|
|
|
NM_001291303.3(FAT4):c.539A>G (p.Asn180Ser)
|
|
|
NM_001291303.3(FAT4):c.5402G>A (p.Arg1801Gln)
|
|
|
NM_001291303.3(FAT4):c.5402G>T (p.Arg1801Leu)
|
|
|
NM_001291303.3(FAT4):c.5403G>A (p.Arg1801=)
|
|
|
NM_001291303.3(FAT4):c.5416C>T (p.Arg1806Cys)
|
|
|
NM_001291303.3(FAT4):c.5418C>A (p.Arg1806=)
|
|
|
NM_001291303.3(FAT4):c.5420G>A (p.Arg1807His)
|
|
|
NM_001291303.3(FAT4):c.5424C>T (p.Ser1808=)
|
|
|
NM_001291303.3(FAT4):c.5431T>G (p.Ser1811Ala)
|
|
|
NM_001291303.3(FAT4):c.5433A>G (p.Ser1811=)
|
|
|
NM_001291303.3(FAT4):c.544G>T (p.Ala182Ser)
|
|
|
NM_001291303.3(FAT4):c.5450A>C (p.Asp1817Ala)
|
rs759964132
|
|
NM_001291303.3(FAT4):c.5450A>G (p.Asp1817Gly)
|
|
|
NM_001291303.3(FAT4):c.5456G>C (p.Gly1819Ala)
|
|
|
NM_001291303.3(FAT4):c.5464T>A (p.Ser1822Thr)
|
|
|
NM_001291303.3(FAT4):c.5469G>A (p.Ser1823=)
|
|
|
NM_001291303.3(FAT4):c.5469G>C (p.Ser1823=)
|
|
|
NM_001291303.3(FAT4):c.5470G>C (p.Asp1824His)
|
|
|
NM_001291303.3(FAT4):c.5481T>A (p.Ile1827=)
|
rs970545402
|
|
NM_001291303.3(FAT4):c.5484T>C (p.Asn1828=)
|
|
|
NM_001291303.3(FAT4):c.5487C>T (p.Ile1829=)
|
|
|
NM_001291303.3(FAT4):c.5490T>C (p.Thr1830=)
|
|
|
NM_001291303.3(FAT4):c.5495G>T (p.Ser1832Ile)
|
|
|
NM_001291303.3(FAT4):c.5505T>A (p.Asn1835Lys)
|
rs2126019806
|
|
NM_001291303.3(FAT4):c.5512A>G (p.Thr1838Ala)
|
|
|
NM_001291303.3(FAT4):c.5515C>A (p.Pro1839Thr)
|
|
|
NM_001291303.3(FAT4):c.5533G>A (p.Val1845Met)
|
rs1179341769
|
|
NM_001291303.3(FAT4):c.5539T>C (p.Ser1847Pro)
|
|
|
NM_001291303.3(FAT4):c.5548A>C (p.Ile1850Leu)
|
|
|
NM_001291303.3(FAT4):c.5551C>T (p.Pro1851Ser)
|
|
|
NM_001291303.3(FAT4):c.5553T>G (p.Pro1851=)
|
rs2126019880
|
|
NM_001291303.3(FAT4):c.5565C>T (p.Ile1855=)
|
|
|
NM_001291303.3(FAT4):c.5569+14C>T
|
|
|
NM_001291303.3(FAT4):c.5569+16C>G
|
|
|
NM_001291303.3(FAT4):c.5569G>C (p.Gly1857Arg)
|
|
|
NM_001291303.3(FAT4):c.556C>G (p.Arg186Gly)
|
|
|
NM_001291303.3(FAT4):c.556C>T (p.Arg186Cys)
|
rs577129552
|
|
NM_001291303.3(FAT4):c.5570-10C>A
|
|
|
NM_001291303.3(FAT4):c.5570-20T>G
|
|
|
NM_001291303.3(FAT4):c.5573C>A (p.Ser1858Tyr)
|
|
|
NM_001291303.3(FAT4):c.5573C>G (p.Ser1858Cys)
|
rs749313432
|
|
NM_001291303.3(FAT4):c.5573C>T (p.Ser1858Phe)
|
rs749313432
|
|
NM_001291303.3(FAT4):c.5581G>A (p.Ala1861Thr)
|
|
|
NM_001291303.3(FAT4):c.55C>T (p.Leu19=)
|
|
|
NM_001291303.3(FAT4):c.565A>T (p.Ile189Phe)
|
|
|
NM_001291303.3(FAT4):c.5661C>A (p.Gly1887=)
|
|
|
NM_001291303.3(FAT4):c.5680A>G (p.Ile1894Val)
|
|
|
NM_001291303.3(FAT4):c.5681T>C (p.Ile1894Thr)
|
|
|
NM_001291303.3(FAT4):c.5689G>A (p.Val1897Ile)
|
rs2126021166
|
|
NM_001291303.3(FAT4):c.5689G>T (p.Val1897Phe)
|
rs2126021166
|
|
NM_001291303.3(FAT4):c.568A>G (p.Thr190Ala)
|
|
|
NM_001291303.3(FAT4):c.569C>T (p.Thr190Ile)
|
|
|
NM_001291303.3(FAT4):c.5704C>A (p.Arg1902=)
|
|
|
NM_001291303.3(FAT4):c.5706A>T (p.Arg1902=)
|
|
|
NM_001291303.3(FAT4):c.5708T>C (p.Leu1903Ser)
|
rs777160179
|
|
NM_001291303.3(FAT4):c.5714A>T (p.Asp1905Val)
|
rs2126021199
|
|
NM_001291303.3(FAT4):c.5716T>C (p.Tyr1906His)
|
|
|
NM_001291303.3(FAT4):c.5721A>C (p.Glu1907Asp)
|
|
|
NM_001291303.3(FAT4):c.5727G>A (p.Gln1909=)
|
|
|
NM_001291303.3(FAT4):c.572T>C (p.Leu191Pro)
|
|
|
NM_001291303.3(FAT4):c.5733T>C (p.Tyr1911=)
|
|
|
NM_001291303.3(FAT4):c.5737A>T (p.Ile1913Phe)
|
|
|
NM_001291303.3(FAT4):c.5739C>T (p.Ile1913=)
|
|
|
NM_001291303.3(FAT4):c.5750G>A (p.Arg1917Gln)
|
|
|
NM_001291303.3(FAT4):c.5754A>G (p.Ala1918=)
|
|
|
NM_001291303.3(FAT4):c.5760_5761inv (p.Gly1921Ser)
|
|
|
NM_001291303.3(FAT4):c.5767G>A (p.Gly1923Arg)
|
|
|
NM_001291303.3(FAT4):c.5768del (p.Gly1923fs)
|
|
|
NM_001291303.3(FAT4):c.5769A>G (p.Gly1923=)
|
|
|
NM_001291303.3(FAT4):c.5780C>T (p.Thr1927Ile)
|
rs1473579499
|
|
NM_001291303.3(FAT4):c.5786G>T (p.Arg1929Ile)
|
|
|
NM_001291303.3(FAT4):c.5811A>G (p.Val1937=)
|
|
|
NM_001291303.3(FAT4):c.5814T>C (p.Asn1938=)
|
rs749564131
|
|
NM_001291303.3(FAT4):c.5824C>A (p.Pro1942Thr)
|
|
|
NM_001291303.3(FAT4):c.5838G>T (p.Leu1946Phe)
|
|
|
NM_001291303.3(FAT4):c.5847C>T (p.Tyr1949=)
|
|
|
NM_001291303.3(FAT4):c.5849G>A (p.Ser1950Asn)
|
|
|
NM_001291303.3(FAT4):c.5867A>C (p.Asn1956Thr)
|
rs1734726577
|
|
NM_001291303.3(FAT4):c.5869C>T (p.Leu1957=)
|
|
|
NM_001291303.3(FAT4):c.587A>T (p.Glu196Val)
|
|
|
NM_001291303.3(FAT4):c.5880A>T (p.Gly1960=)
|
rs756664489
|
|
NM_001291303.3(FAT4):c.5889_5890delinsAA (p.Leu1964Ile)
|
rs2126021497
|
|
NM_001291303.3(FAT4):c.5904T>C (p.Val1968=)
|
rs2126021524
|
|
NM_001291303.3(FAT4):c.5906C>T (p.Thr1969Ile)
|
|
|
NM_001291303.3(FAT4):c.5910T>C (p.Asp1970=)
|
|
|
NM_001291303.3(FAT4):c.5920+11_5920+15del
|
|
|
NM_001291303.3(FAT4):c.5920+314del
|
rs147990721
|
|
NM_001291303.3(FAT4):c.5920+9T>C
|
|
|
NM_001291303.3(FAT4):c.5921-11T>G
|
rs2126026739
|
|
NM_001291303.3(FAT4):c.5921-12C>T
|
|
|
NM_001291303.3(FAT4):c.5921-14C>G
|
|
|
NM_001291303.3(FAT4):c.593C>T (p.Ala198Val)
|
|
|
NM_001291303.3(FAT4):c.5942A>T (p.Tyr1981Phe)
|
|
|
NM_001291303.3(FAT4):c.5950G>A (p.Ala1984Thr)
|
|
|
NM_001291303.3(FAT4):c.5955A>C (p.Ser1985=)
|
|
|
NM_001291303.3(FAT4):c.5990A>G (p.Asn1997Ser)
|
|
|
NM_001291303.3(FAT4):c.6008T>G (p.Leu2003Arg)
|
rs2126026943
|
|
NM_001291303.3(FAT4):c.6022C>T (p.Arg2008Trp)
|
|
|
NM_001291303.3(FAT4):c.6024G>A (p.Arg2008=)
|
|
|
NM_001291303.3(FAT4):c.6048G>A (p.Leu2016=)
|
|
|
NM_001291303.3(FAT4):c.6075G>A (p.Gln2025=)
|
|
|
NM_001291303.3(FAT4):c.6092T>C (p.Phe2031Ser)
|
|
|
NM_001291303.3(FAT4):c.6099C>T (p.Ser2033=)
|
rs1734990759
|
|
NM_001291303.3(FAT4):c.6111C>T (p.Val2037=)
|
|
|
NM_001291303.3(FAT4):c.613A>G (p.Lys205Glu)
|
|
|
NM_001291303.3(FAT4):c.6147G>A (p.Pro2049=)
|
|
|
NM_001291303.3(FAT4):c.6148A>G (p.Thr2050Ala)
|
|
|
NM_001291303.3(FAT4):c.6171A>C (p.Thr2057=)
|
|
|
NM_001291303.3(FAT4):c.6171A>G (p.Thr2057=)
|
|
|
NM_001291303.3(FAT4):c.6174C>T (p.Tyr2058=)
|
|
|
NM_001291303.3(FAT4):c.6177T>C (p.Ile2059=)
|
|
|
NM_001291303.3(FAT4):c.6189A>C (p.Thr2063=)
|
|
|
NM_001291303.3(FAT4):c.618C>A (p.Gly206=)
|
|
|
NM_001291303.3(FAT4):c.6193A>G (p.Ile2065Val)
|
|
|
NM_001291303.3(FAT4):c.61G>C (p.Val21Leu)
|
|
|
NM_001291303.3(FAT4):c.6200C>T (p.Thr2067Ile)
|
rs2126027195
|
|
NM_001291303.3(FAT4):c.6204T>C (p.Val2068=)
|
|
|
NM_001291303.3(FAT4):c.6228C>T (p.Asp2076=)
|
|
|
NM_001291303.3(FAT4):c.6234T>C (p.Asp2078=)
|
rs1578616858
|
|
NM_001291303.3(FAT4):c.6254T>G (p.Ile2085Ser)
|
|
|
NM_001291303.3(FAT4):c.6258G>A (p.Glu2086=)
|
|
|
NM_001291303.3(FAT4):c.6262A>T (p.Thr2088Ser)
|
|
|
NM_001291303.3(FAT4):c.629G>T (p.Arg210Leu)
|
rs1353199749
|
|
NM_001291303.3(FAT4):c.6303C>T (p.Thr2101=)
|
|
|
NM_001291303.3(FAT4):c.6308A>G (p.Asp2103Gly)
|
rs112252276
|
|
NM_001291303.3(FAT4):c.6311G>A (p.Gly2104Asp)
|
|
|
NM_001291303.3(FAT4):c.6327T>C (p.Thr2109=)
|
|
|
NM_001291303.3(FAT4):c.6339C>T (p.Asp2113=)
|
|
|
NM_001291303.3(FAT4):c.633G>A (p.Glu211=)
|
|
|
NM_001291303.3(FAT4):c.6343G>A (p.Glu2115Lys)
|
|
|
NM_001291303.3(FAT4):c.634G>T (p.Val212Phe)
|
rs2125938960
|
|
NM_001291303.3(FAT4):c.6373G>T (p.Val2125Leu)
|
|
|
NM_001291303.3(FAT4):c.6394C>A (p.Pro2132Thr)
|
|
|
NM_001291303.3(FAT4):c.6412A>G (p.Thr2138Ala)
|
|
|
NM_001291303.3(FAT4):c.6414A>C (p.Thr2138=)
|
|
|
NM_001291303.3(FAT4):c.6417G>A (p.Glu2139=)
|
|
|
NM_001291303.3(FAT4):c.6423A>G (p.Val2141=)
|
|
|
NM_001291303.3(FAT4):c.6424G>T (p.Val2142Phe)
|
|
|
NM_001291303.3(FAT4):c.6432A>G (p.Val2144=)
|
|
|
NM_001291303.3(FAT4):c.6436G>T (p.Asp2146Tyr)
|
|
|
NM_001291303.3(FAT4):c.6462T>C (p.Phe2154=)
|
|
|
NM_001291303.3(FAT4):c.6468A>G (p.Gln2156=)
|
|
|
NM_001291303.3(FAT4):c.6471T>C (p.Ala2157=)
|
|
|
NM_001291303.3(FAT4):c.6483G>A (p.Val2161=)
|
|
|
NM_001291303.3(FAT4):c.6491A>G (p.Asn2164Ser)
|
|
|
NM_001291303.3(FAT4):c.6498C>T (p.Asn2166=)
|
|
|
NM_001291303.3(FAT4):c.6518T>C (p.Ile2173Thr)
|
rs1236758384
|
|
NM_001291303.3(FAT4):c.6522A>G (p.Ile2174Met)
|
|
|
NM_001291303.3(FAT4):c.6525A>T (p.Gln2175His)
|
rs746388291
|
|
NM_001291303.3(FAT4):c.6554C>A (p.Thr2185Lys)
|
rs1553968839
|
|
NM_001291303.3(FAT4):c.6569G>A (p.Arg2190His)
|
|
|
NM_001291303.3(FAT4):c.6592A>G (p.Thr2198Ala)
|
rs2126027812
|
|
NM_001291303.3(FAT4):c.659T>C (p.Val220Ala)
|
|
|
NM_001291303.3(FAT4):c.6609G>T (p.Arg2203=)
|
|
|
NM_001291303.3(FAT4):c.6616T>A (p.Ser2206Thr)
|
|
|
NM_001291303.3(FAT4):c.6618T>C (p.Ser2206=)
|
rs1735020530
|
|
NM_001291303.3(FAT4):c.6638T>C (p.Val2213Ala)
|
|
|
NM_001291303.3(FAT4):c.6640G>T (p.Ala2214Ser)
|
rs149686118
|
|
NM_001291303.3(FAT4):c.6666C>T (p.Thr2222=)
|
|
|
NM_001291303.3(FAT4):c.6688_6690delinsTTT (p.Gln2230Phe)
|
|
|
NM_001291303.3(FAT4):c.6693A>G (p.Ala2231=)
|
|
|
NM_001291303.3(FAT4):c.6700C>T (p.Arg2234Ter)
|
rs567305960
|
|
NM_001291303.3(FAT4):c.6719C>T (p.Thr2240Ile)
|
rs774192877
|
|
NM_001291303.3(FAT4):c.6721G>T (p.Asp2241Tyr)
|
|
|
NM_001291303.3(FAT4):c.6747A>C (p.Leu2249=)
|
|
|
NM_001291303.3(FAT4):c.6771T>C (p.Pro2257=)
|
rs2126028086
|
|
NM_001291303.3(FAT4):c.6800A>G (p.Asn2267Ser)
|
|
|
NM_001291303.3(FAT4):c.6815T>C (p.Leu2272Ser)
|
|
|
NM_001291303.3(FAT4):c.6816A>G (p.Leu2272=)
|
|
|
NM_001291303.3(FAT4):c.6822A>G (p.Thr2274=)
|
|
|
NM_001291303.3(FAT4):c.6825A>G (p.Leu2275=)
|
|
|
NM_001291303.3(FAT4):c.6832A>T (p.Thr2278Ser)
|
rs775172064
|
|
NM_001291303.3(FAT4):c.6843+10_6843+57del
|
rs2126028203
|
|
NM_001291303.3(FAT4):c.6843+19A>G
|
|
|
NM_001291303.3(FAT4):c.6843+1G>T
|
rs2126028189
|
|
NM_001291303.3(FAT4):c.6843+20G>A
|
|
|
NM_001291303.3(FAT4):c.6843+4A>G
|
|
|
NM_001291303.3(FAT4):c.6843+8T>G
|
rs2126028200
|
|
NM_001291303.3(FAT4):c.6843+9A>G
|
|
|
NM_001291303.3(FAT4):c.6844-10T>C
|
|
|
NM_001291303.3(FAT4):c.6844-17T>C
|
|
|
NM_001291303.3(FAT4):c.6844-4A>G
|
|
|
NM_001291303.3(FAT4):c.6844-6C>T
|
|
|
NM_001291303.3(FAT4):c.6849G>T (p.Val2283=)
|
rs943662980
|
|
NM_001291303.3(FAT4):c.6851C>T (p.Ala2284Val)
|
rs2126028801
|
|
NM_001291303.3(FAT4):c.6855A>G (p.Arg2285=)
|
|
|
NM_001291303.3(FAT4):c.6866G>A (p.Arg2289Gln)
|
|
|
NM_001291303.3(FAT4):c.6883C>T (p.Leu2295Phe)
|
rs2126028825
|
|
NM_001291303.3(FAT4):c.6888A>G (p.Ser2296=)
|
|
|
NM_001291303.3(FAT4):c.6905G>A (p.Gly2302Asp)
|
rs143204873
|
|
NM_001291303.3(FAT4):c.6905G>C (p.Gly2302Ala)
|
rs143204873
|
|
NM_001291303.3(FAT4):c.6909T>C (p.Asn2303=)
|
|
|
NM_001291303.3(FAT4):c.6913G>A (p.Asp2305Asn)
|
|
|
NM_001291303.3(FAT4):c.6937A>G (p.Ser2313Gly)
|
|
|
NM_001291303.3(FAT4):c.6938G>A (p.Ser2313Asn)
|
rs2126028937
|
|
NM_001291303.3(FAT4):c.693G>T (p.Arg231=)
|
|
|
NM_001291303.3(FAT4):c.6951A>G (p.Gly2317=)
|
|
|
NM_001291303.3(FAT4):c.698A>G (p.Tyr233Cys)
|
rs756400976
|
|
NM_001291303.3(FAT4):c.6991G>A (p.Val2331Ile)
|
rs752320782
|
|
NM_001291303.3(FAT4):c.6997A>G (p.Met2333Val)
|
|
|
NM_001291303.3(FAT4):c.7010C>T (p.Thr2337Ile)
|
|
|
NM_001291303.3(FAT4):c.7018+16C>T
|
|
|
NM_001291303.3(FAT4):c.7018+2T>C
|
|
|
NM_001291303.3(FAT4):c.7018+7C>A
|
|
|
NM_001291303.3(FAT4):c.7019-16T>C
|
|
|
NM_001291303.3(FAT4):c.7019-18A>G
|
|
|
NM_001291303.3(FAT4):c.7019-3T>G
|
|
|
NM_001291303.3(FAT4):c.7019-4_7019-3dup
|
rs780046426
|
|
NM_001291303.3(FAT4):c.7020A>G (p.Gly2340=)
|
|
|
NM_001291303.3(FAT4):c.7028C>A (p.Ala2343Asp)
|
|
|
NM_001291303.3(FAT4):c.7028C>T (p.Ala2343Val)
|
|
|
NM_001291303.3(FAT4):c.7054G>A (p.Val2352Ile)
|
|
|
NM_001291303.3(FAT4):c.7060G>T (p.Val2354Leu)
|
|
|
NM_001291303.3(FAT4):c.7098T>C (p.Ser2366=)
|
|
|
NM_001291303.3(FAT4):c.7103C>T (p.Ala2368Val)
|
rs116568645
|
|
NM_001291303.3(FAT4):c.7104G>A (p.Ala2368=)
|
|
|
NM_001291303.3(FAT4):c.7131A>C (p.Ala2377=)
|
|
|
NM_001291303.3(FAT4):c.7132C>T (p.Pro2378Ser)
|
|
|
NM_001291303.3(FAT4):c.7133C>A (p.Pro2378Gln)
|
|
|
NM_001291303.3(FAT4):c.7140A>C (p.Gly2380=)
|
|
|
NM_001291303.3(FAT4):c.7142C>A (p.Thr2381Lys)
|
|
|
NM_001291303.3(FAT4):c.7151T>C (p.Leu2384Ser)
|
|
|
NM_001291303.3(FAT4):c.7163C>G (p.Ala2388Gly)
|
|
|
NM_001291303.3(FAT4):c.7170T>C (p.Asp2390=)
|
|
|
NM_001291303.3(FAT4):c.7177G>A (p.Ala2393Thr)
|
|
|
NM_001291303.3(FAT4):c.7189G>A (p.Ala2397Thr)
|
rs1725381092
|
|
NM_001291303.3(FAT4):c.7190C>T (p.Ala2397Val)
|
|
|
NM_001291303.3(FAT4):c.7191A>G (p.Ala2397=)
|
|
|
NM_001291303.3(FAT4):c.7199+16T>A
|
|
|
NM_001291303.3(FAT4):c.7212C>T (p.Ile2404=)
|
|
|
NM_001291303.3(FAT4):c.7213G>A (p.Gly2405Ser)
|
|
|
NM_001291303.3(FAT4):c.7233G>A (p.Thr2411=)
|
rs762694598
|
|
NM_001291303.3(FAT4):c.7233G>C (p.Thr2411=)
|
|
|
NM_001291303.3(FAT4):c.7240C>G (p.Pro2414Ala)
|
|
|
NM_001291303.3(FAT4):c.7241C>T (p.Pro2414Leu)
|
|
|
NM_001291303.3(FAT4):c.7244C>T (p.Ser2415Leu)
|
|
|
NM_001291303.3(FAT4):c.7245G>T (p.Ser2415=)
|
|
|
NM_001291303.3(FAT4):c.7248A>G (p.Thr2416=)
|
|
|
NM_001291303.3(FAT4):c.7251A>G (p.Gly2417=)
|
|
|
NM_001291303.3(FAT4):c.7263C>T (p.Thr2421=)
|
|
|
NM_001291303.3(FAT4):c.7267G>A (p.Ala2423Thr)
|
rs776977766
|
|
NM_001291303.3(FAT4):c.727A>G (p.Ile243Val)
|
rs2125939075
|
|
NM_001291303.3(FAT4):c.7298A>T (p.Tyr2433Phe)
|
rs776198713
|
|
NM_001291303.3(FAT4):c.7299T>C (p.Tyr2433=)
|
|
|
NM_001291303.3(FAT4):c.7305G>A (p.Leu2435=)
|
|
|
NM_001291303.3(FAT4):c.7323T>C (p.Asp2441=)
|
rs142184187
|
|
NM_001291303.3(FAT4):c.7335A>G (p.Pro2445=)
|
|
|
NM_001291303.3(FAT4):c.7382T>A (p.Val2461Asp)
|
|
|
NM_001291303.3(FAT4):c.7386T>C (p.Asn2462=)
|
|
|
NM_001291303.3(FAT4):c.738C>T (p.Asn246=)
|
|
|
NM_001291303.3(FAT4):c.7395A>G (p.Pro2465=)
|
|
|
NM_001291303.3(FAT4):c.739C>A (p.Pro247Thr)
|
rs191329848
|
|
NM_001291303.3(FAT4):c.739C>T (p.Pro247Ser)
|
rs191329848
|
|
NM_001291303.3(FAT4):c.7450+15T>C
|
rs2126054919
|
|
NM_001291303.3(FAT4):c.7451-15C>T
|
|
|
NM_001291303.3(FAT4):c.7451-17C>G
|
|
|
NM_001291303.3(FAT4):c.7451-5T>A
|
|
|
NM_001291303.3(FAT4):c.7451G>C (p.Gly2484Ala)
|
rs2126056595
|
|
NM_001291303.3(FAT4):c.7454C>T (p.Ser2485Phe)
|
rs2126056606
|
|
NM_001291303.3(FAT4):c.7461C>A (p.Val2487=)
|
|
|
NM_001291303.3(FAT4):c.7466C>A (p.Ala2489Glu)
|
rs144853732
|
|
NM_001291303.3(FAT4):c.7466C>T (p.Ala2489Val)
|
rs144853732
|
|
NM_001291303.3(FAT4):c.7490T>C (p.Ile2497Thr)
|
|
|
NM_001291303.3(FAT4):c.7504G>T (p.Glu2502Ter)
|
|
|
NM_001291303.3(FAT4):c.7506A>G (p.Glu2502=)
|
|
|
NM_001291303.3(FAT4):c.7518T>C (p.Ser2506=)
|
|
|
NM_001291303.3(FAT4):c.7524G>C (p.Ser2508=)
|
|
|
NM_001291303.3(FAT4):c.7542A>C (p.Lys2514Asn)
|
|
|
NM_001291303.3(FAT4):c.7542A>T (p.Lys2514Asn)
|
|
|
NM_001291303.3(FAT4):c.7553A>G (p.Asp2518Gly)
|
|
|
NM_001291303.3(FAT4):c.7566A>G (p.Gly2522=)
|
rs1279846632
|
|
NM_001291303.3(FAT4):c.7569C>T (p.Ala2523=)
|
|
|
NM_001291303.3(FAT4):c.7577C>T (p.Ala2526Val)
|
|
|
NM_001291303.3(FAT4):c.7581C>T (p.Ala2527=)
|
|
|
NM_001291303.3(FAT4):c.7590A>G (p.Leu2530=)
|
|
|
NM_001291303.3(FAT4):c.7593C>G (p.Asn2531Lys)
|
|
|
NM_001291303.3(FAT4):c.7593C>T (p.Asn2531=)
|
rs367971071
|
|
NM_001291303.3(FAT4):c.7595G>A (p.Gly2532Glu)
|
rs2126056817
|
|
NM_001291303.3(FAT4):c.7601C>T (p.Ser2534Leu)
|
rs2126056821
|
|
NM_001291303.3(FAT4):c.760C>T (p.His254Tyr)
|
rs2125939121
|
|
NM_001291303.3(FAT4):c.7611A>C (p.Thr2537=)
|
|
|
NM_001291303.3(FAT4):c.7611A>G (p.Thr2537=)
|
|
|
NM_001291303.3(FAT4):c.7611A>T (p.Thr2537=)
|
|
|
NM_001291303.3(FAT4):c.7621C>T (p.His2541Tyr)
|
rs2126056853
|
|
NM_001291303.3(FAT4):c.7626A>G (p.Val2542=)
|
|
|
NM_001291303.3(FAT4):c.7628A>C (p.Lys2543Thr)
|
rs2126056866
|
|
NM_001291303.3(FAT4):c.7653A>G (p.Thr2551=)
|
|
|
NM_001291303.3(FAT4):c.7659T>C (p.Ser2553=)
|
|
|
NM_001291303.3(FAT4):c.7669A>G (p.Thr2557Ala)
|
|
|
NM_001291303.3(FAT4):c.7670del (p.Thr2557fs)
|
|
|
NM_001291303.3(FAT4):c.7681G>A (p.Val2561Met)
|
|
|
NM_001291303.3(FAT4):c.7681G>C (p.Val2561Leu)
|
|
|
NM_001291303.3(FAT4):c.7692C>T (p.Ala2564=)
|
rs780699634
|
|
NM_001291303.3(FAT4):c.7693G>T (p.Asp2565Tyr)
|
|
|
NM_001291303.3(FAT4):c.7699C>T (p.Pro2567Ser)
|
|
|
NM_001291303.3(FAT4):c.7707G>T (p.Val2569=)
|
rs988863
|
|
NM_001291303.3(FAT4):c.7717G>A (p.Glu2573Lys)
|
rs2126056985
|
|
NM_001291303.3(FAT4):c.7718A>G (p.Glu2573Gly)
|
|
|
NM_001291303.3(FAT4):c.771G>A (p.Ala257=)
|
|
|
NM_001291303.3(FAT4):c.7725G>C (p.Thr2575=)
|
|
|
NM_001291303.3(FAT4):c.772G>C (p.Gly258Arg)
|
|
|
NM_001291303.3(FAT4):c.7746A>G (p.Gln2582=)
|
|
|
NM_001291303.3(FAT4):c.7755C>T (p.Ser2585=)
|
|
|
NM_001291303.3(FAT4):c.7757C>A (p.Ser2586Tyr)
|
|
|
NM_001291303.3(FAT4):c.7757C>G (p.Ser2586Cys)
|
rs370451325
|
|
NM_001291303.3(FAT4):c.775G>T (p.Val259Leu)
|
rs945517445
|
|
NM_001291303.3(FAT4):c.7777G>A (p.Gly2593Arg)
|
|
|
NM_001291303.3(FAT4):c.7782C>G (p.Ser2594=)
|
|
|
NM_001291303.3(FAT4):c.7786T>C (p.Leu2596=)
|
|
|
NM_001291303.3(FAT4):c.778C>A (p.Pro260Thr)
|
|
|
NM_001291303.3(FAT4):c.7795G>A (p.Glu2599Lys)
|
|
|
NM_001291303.3(FAT4):c.7799C>T (p.Pro2600Leu)
|
|
|
NM_001291303.3(FAT4):c.7805C>T (p.Ser2602Leu)
|
|
|
NM_001291303.3(FAT4):c.780T>G (p.Pro260=)
|
|
|
NM_001291303.3(FAT4):c.7815C>A (p.Ile2605=)
|
rs201257189
|
|
NM_001291303.3(FAT4):c.7815C>T (p.Ile2605=)
|
rs201257189
|
|
NM_001291303.3(FAT4):c.7831G>A (p.Gly2611Ser)
|
rs2126057163
|
|
NM_001291303.3(FAT4):c.7837A>G (p.Thr2613Ala)
|
|
|
NM_001291303.3(FAT4):c.7839T>C (p.Thr2613=)
|
|
|
NM_001291303.3(FAT4):c.7845G>A (p.Gln2615=)
|
|
|
NM_001291303.3(FAT4):c.7854G>C (p.Gln2618His)
|
|
|
NM_001291303.3(FAT4):c.7875T>C (p.Ile2625=)
|
|
|
NM_001291303.3(FAT4):c.78A>G (p.Arg26=)
|
|
|
NM_001291303.3(FAT4):c.7905A>G (p.Gln2635=)
|
|
|
NM_001291303.3(FAT4):c.7915G>T (p.Val2639Leu)
|
|
|
NM_001291303.3(FAT4):c.7919G>A (p.Trp2640Ter)
|
|
|
NM_001291303.3(FAT4):c.7949C>T (p.Pro2650Leu)
|
rs2126057386
|
|
NM_001291303.3(FAT4):c.7956C>T (p.Ser2652=)
|
|
|
NM_001291303.3(FAT4):c.7968A>G (p.Lys2656=)
|
|
|
NM_001291303.3(FAT4):c.7969C>G (p.Leu2657Val)
|
rs2126057416
|
|
NM_001291303.3(FAT4):c.7979C>G (p.Thr2660Arg)
|
rs761286125
|
|
NM_001291303.3(FAT4):c.7979C>T (p.Thr2660Ile)
|
|
|
NM_001291303.3(FAT4):c.7980A>C (p.Thr2660=)
|
|
|
NM_001291303.3(FAT4):c.8007A>C (p.Pro2669=)
|
|
|
NM_001291303.3(FAT4):c.8008A>G (p.Ile2670Val)
|
|
|
NM_001291303.3(FAT4):c.8034T>C (p.Ser2678=)
|
|
|
NM_001291303.3(FAT4):c.8049C>T (p.Asn2683=)
|
|
|
NM_001291303.3(FAT4):c.8057_8059del (p.Pro2686del)
|
|
|
NM_001291303.3(FAT4):c.8062A>G (p.Lys2688Glu)
|
|
|
NM_001291303.3(FAT4):c.8072C>T (p.Thr2691Ile)
|
|
|
NM_001291303.3(FAT4):c.8083A>G (p.Met2695Val)
|
|
|
NM_001291303.3(FAT4):c.812A>G (p.Gln271Arg)
|
|
|
NM_001291303.3(FAT4):c.8155A>C (p.Ser2719Arg)
|
|
|
NM_001291303.3(FAT4):c.8156G>A (p.Ser2719Asn)
|
rs1415356153
|
|
NM_001291303.3(FAT4):c.815T>C (p.Val272Ala)
|
rs1313831836
|
|
NM_001291303.3(FAT4):c.8160C>A (p.Ile2720=)
|
|
|
NM_001291303.3(FAT4):c.8187C>T (p.Ser2729=)
|
|
|
NM_001291303.3(FAT4):c.8188G>A (p.Val2730Ile)
|
|
|
NM_001291303.3(FAT4):c.8197T>C (p.Leu2733=)
|
|
|
NM_001291303.3(FAT4):c.8211A>G (p.Lys2737=)
|
|
|
NM_001291303.3(FAT4):c.8220T>C (p.His2740=)
|
|
|
NM_001291303.3(FAT4):c.8241A>G (p.Ser2747=)
|
rs2126057778
|
|
NM_001291303.3(FAT4):c.8247C>G (p.Asp2749Glu)
|
rs1725949849
|
|
NM_001291303.3(FAT4):c.8251G>C (p.Gly2751Arg)
|
rs1469626568
|
|
NM_001291303.3(FAT4):c.8259G>A (p.Pro2753=)
|
|
|
NM_001291303.3(FAT4):c.8259G>C (p.Pro2753=)
|
|
|
NM_001291303.3(FAT4):c.8266A>G (p.Ser2756Gly)
|
|
|
NM_001291303.3(FAT4):c.8283C>A (p.Val2761=)
|
|
|
NM_001291303.3(FAT4):c.8285T>G (p.Met2762Arg)
|
|
|
NM_001291303.3(FAT4):c.8315C>A (p.Ala2772Asp)
|
|
|
NM_001291303.3(FAT4):c.8332A>G (p.Ile2778Val)
|
rs773858750
|
|
NM_001291303.3(FAT4):c.8336T>G (p.Phe2779Cys)
|
|
|
NM_001291303.3(FAT4):c.8338A>G (p.Ser2780Gly)
|
|
|
NM_001291303.3(FAT4):c.8340T>A (p.Ser2780Arg)
|
|
|
NM_001291303.3(FAT4):c.8344C>A (p.His2782Asn)
|
|
|
NM_001291303.3(FAT4):c.8344C>T (p.His2782Tyr)
|
rs776841261
|
|
NM_001291303.3(FAT4):c.8346T>C (p.His2782=)
|
|
|
NM_001291303.3(FAT4):c.835G>T (p.Glu279Ter)
|
rs373298045
|
|
NM_001291303.3(FAT4):c.8363C>G (p.Pro2788Arg)
|
rs267600011
|
|
NM_001291303.3(FAT4):c.8372A>T (p.Tyr2791Phe)
|
|
|
NM_001291303.3(FAT4):c.8373C>T (p.Tyr2791=)
|
rs1725957299
|
|
NM_001291303.3(FAT4):c.837G>A (p.Glu279=)
|
|
|
NM_001291303.3(FAT4):c.8383C>T (p.Arg2795Cys)
|
|
|
NM_001291303.3(FAT4):c.8388C>A (p.Val2796=)
|
rs2126058061
|
|
NM_001291303.3(FAT4):c.8417A>C (p.Asn2806Thr)
|
rs1725960134
|
|
NM_001291303.3(FAT4):c.8423T>C (p.Ile2808Thr)
|
|
|
NM_001291303.3(FAT4):c.8441T>C (p.Met2814Thr)
|
|
|
NM_001291303.3(FAT4):c.8444A>G (p.Asp2815Gly)
|
rs763149272
|
|
NM_001291303.3(FAT4):c.8447C>T (p.Ala2816Val)
|
|
|
NM_001291303.3(FAT4):c.8450G>A (p.Ser2817Asn)
|
|
|
NM_001291303.3(FAT4):c.8456C>A (p.Pro2819Gln)
|
rs1423578835
|
|
NM_001291303.3(FAT4):c.847G>A (p.Ala283Thr)
|
|
|
NM_001291303.3(FAT4):c.848C>T (p.Ala283Val)
|
rs2125939276
|
|
NM_001291303.3(FAT4):c.8495G>T (p.Ser2832Ile)
|
rs778678016
|
|
NM_001291303.3(FAT4):c.8508T>C (p.Asn2836=)
|
|
|
NM_001291303.3(FAT4):c.8509A>C (p.Arg2837=)
|
|
|
NM_001291303.3(FAT4):c.8518A>C (p.Thr2840Pro)
|
|
|
NM_001291303.3(FAT4):c.8536C>T (p.Arg2846Ter)
|
|
|
NM_001291303.3(FAT4):c.8545G>A (p.Ala2849Thr)
|
rs181821271
|
|
NM_001291303.3(FAT4):c.8556T>G (p.Ser2852=)
|
|
|
NM_001291303.3(FAT4):c.8573_8574del (p.Thr2858fs)
|
|
|
NM_001291303.3(FAT4):c.858C>A (p.Arg286=)
|
|
|
NM_001291303.3(FAT4):c.8599A>C (p.Ile2867Leu)
|
|
|
NM_001291303.3(FAT4):c.8630C>T (p.Thr2877Ile)
|
rs754458048
|
|
NM_001291303.3(FAT4):c.8654A>C (p.Glu2885Ala)
|
|
|
NM_001291303.3(FAT4):c.8666T>C (p.Ile2889Thr)
|
|
|
NM_001291303.3(FAT4):c.867G>T (p.Leu289=)
|
|
|
NM_001291303.3(FAT4):c.8686G>A (p.Val2896Ile)
|
|
|
NM_001291303.3(FAT4):c.8709G>A (p.Glu2903=)
|
|
|
NM_001291303.3(FAT4):c.8720G>C (p.Gly2907Ala)
|
|
|
NM_001291303.3(FAT4):c.8738T>G (p.Ile2913Arg)
|
|
|
NM_001291303.3(FAT4):c.873C>A (p.Asp291Glu)
|
|
|
NM_001291303.3(FAT4):c.8761A>G (p.Arg2921Gly)
|
rs2126058590
|
|
NM_001291303.3(FAT4):c.876G>A (p.Glu292=)
|
|
|
NM_001291303.3(FAT4):c.8771C>G (p.Ala2924Gly)
|
|
|
NM_001291303.3(FAT4):c.8792A>G (p.Asn2931Ser)
|
|
|
NM_001291303.3(FAT4):c.8801T>A (p.Ile2934Asn)
|
|
|
NM_001291303.3(FAT4):c.8810A>G (p.Tyr2937Cys)
|
|
|
NM_001291303.3(FAT4):c.8826C>G (p.Gly2942=)
|
rs1355664497
|
|
NM_001291303.3(FAT4):c.8826C>T (p.Gly2942=)
|
|
|
NM_001291303.3(FAT4):c.8836G>A (p.Val2946Met)
|
|
|
NM_001291303.3(FAT4):c.8838G>A (p.Val2946=)
|
|
|
NM_001291303.3(FAT4):c.8852A>G (p.His2951Arg)
|
|
|
NM_001291303.3(FAT4):c.885C>G (p.Pro295=)
|
|
|
NM_001291303.3(FAT4):c.8862A>G (p.Ile2954Met)
|
|
|
NM_001291303.3(FAT4):c.8865G>A (p.Val2955=)
|
rs773995723
|
|
NM_001291303.3(FAT4):c.8877T>C (p.Asp2959=)
|
|
|
NM_001291303.3(FAT4):c.8887C>T (p.Pro2963Ser)
|
|
|
NM_001291303.3(FAT4):c.8896A>G (p.Ile2966Val)
|
|
|
NM_001291303.3(FAT4):c.8903A>G (p.Glu2968Gly)
|
rs2126058765
|
|
NM_001291303.3(FAT4):c.8920A>C (p.Asn2974His)
|
rs1205109272
|
|
NM_001291303.3(FAT4):c.8933G>C (p.Ser2978Thr)
|
|
|
NM_001291303.3(FAT4):c.8949T>C (p.Pro2983=)
|
|
|
NM_001291303.3(FAT4):c.8963G>C (p.Ser2988Thr)
|
|
|
NM_001291303.3(FAT4):c.8968T>G (p.Tyr2990Asp)
|
|
|
NM_001291303.3(FAT4):c.8975C>T (p.Thr2992Ile)
|
rs925926334
|
|
NM_001291303.3(FAT4):c.8979A>C (p.Pro2993=)
|
|
|
NM_001291303.3(FAT4):c.8981T>G (p.Val2994Gly)
|
|
|
NM_001291303.3(FAT4):c.8993T>C (p.Val2998Ala)
|
|
|
NM_001291303.3(FAT4):c.8996A>C (p.Lys2999Thr)
|
rs2126058886
|
|
NM_001291303.3(FAT4):c.89T>C (p.Leu30Pro)
|
|
|
NM_001291303.3(FAT4):c.9001G>T (p.Gly3001Cys)
|
|
|
NM_001291303.3(FAT4):c.9004A>G (p.Thr3002Ala)
|
rs2126058899
|
|
NM_001291303.3(FAT4):c.9005C>T (p.Thr3002Met)
|
|
|
NM_001291303.3(FAT4):c.9019G>A (p.Val3007Ile)
|
|
|
NM_001291303.3(FAT4):c.9057A>G (p.Ser3019=)
|
rs763659763
|
|
NM_001291303.3(FAT4):c.9084T>C (p.Asp3028=)
|
rs2126058982
|
|
NM_001291303.3(FAT4):c.9087C>A (p.Asn3029Lys)
|
rs201663831
|
|
NM_001291303.3(FAT4):c.9102T>G (p.Phe3034Leu)
|
rs2126059002
|
|
NM_001291303.3(FAT4):c.9120G>A (p.Thr3040=)
|
rs749702080
|
|
NM_001291303.3(FAT4):c.9125G>A (p.Trp3042Ter)
|
|
|
NM_001291303.3(FAT4):c.9137C>G (p.Ala3046Gly)
|
|
|
NM_001291303.3(FAT4):c.9139T>G (p.Ser3047Ala)
|
|
|
NM_001291303.3(FAT4):c.9140C>T (p.Ser3047Phe)
|
rs2126059036
|
|
NM_001291303.3(FAT4):c.9147G>A (p.Leu3049=)
|
|
|
NM_001291303.3(FAT4):c.914T>C (p.Ile305Thr)
|
|
|
NM_001291303.3(FAT4):c.918G>C (p.Thr306=)
|
|
|
NM_001291303.3(FAT4):c.9200G>A (p.Gly3067Glu)
|
rs867017568
|
|
NM_001291303.3(FAT4):c.9222A>G (p.Gln3074=)
|
|
|
NM_001291303.3(FAT4):c.9233A>G (p.His3078Arg)
|
|
|
NM_001291303.3(FAT4):c.9256T>C (p.Tyr3086His)
|
|
|
NM_001291303.3(FAT4):c.927G>T (p.Glu309Asp)
|
|
|
NM_001291303.3(FAT4):c.9300C>T (p.Ile3100=)
|
|
|
NM_001291303.3(FAT4):c.9338T>C (p.Val3113Ala)
|
|
|
NM_001291303.3(FAT4):c.9359C>A (p.Ala3120Glu)
|
|
|
NM_001291303.3(FAT4):c.9362C>T (p.Ala3121Val)
|
|
|
NM_001291303.3(FAT4):c.9363G>A (p.Ala3121=)
|
rs267600012
|
|
NM_001291303.3(FAT4):c.9384C>T (p.Tyr3128=)
|
|
|
NM_001291303.3(FAT4):c.9390TTC[1] (p.Ser3132del)
|
|
|
NM_001291303.3(FAT4):c.9399A>T (p.Gly3133=)
|
|
|
NM_001291303.3(FAT4):c.9402T>C (p.Asn3134=)
|
|
|
NM_001291303.3(FAT4):c.9408A>T (p.Glu3136Asp)
|
|
|
NM_001291303.3(FAT4):c.9412A>G (p.Ile3138Val)
|
|
|
NM_001291303.3(FAT4):c.9423C>A (p.Ile3141=)
|
|
|
NM_001291303.3(FAT4):c.9425A>G (p.Asn3142Ser)
|
rs2126059432
|
|
NM_001291303.3(FAT4):c.9450A>G (p.Leu3150=)
|
|
|
NM_001291303.3(FAT4):c.9454A>G (p.Lys3152Glu)
|
rs1308115647
|
|
NM_001291303.3(FAT4):c.9468T>C (p.Tyr3156=)
|
|
|
NM_001291303.3(FAT4):c.9472C>G (p.Leu3158Val)
|
|
|
NM_001291303.3(FAT4):c.9477C>T (p.Cys3159=)
|
|
|
NM_001291303.3(FAT4):c.947G>A (p.Arg316Gln)
|
|
|
NM_001291303.3(FAT4):c.947G>T (p.Arg316Leu)
|
|
|
NM_001291303.3(FAT4):c.9487G>A (p.Glu3163Lys)
|
|
|
NM_001291303.3(FAT4):c.9495G>A (p.Thr3165=)
|
|
|
NM_001291303.3(FAT4):c.9496_9497delinsGC (p.Ile3166Ala)
|
rs2126059532
|
|
NM_001291303.3(FAT4):c.9503C>G (p.Ala3168Gly)
|
rs1167760725
|
|
NM_001291303.3(FAT4):c.9505A>G (p.Ile3169Val)
|
|
|
NM_001291303.3(FAT4):c.9517T>G (p.Trp3173Gly)
|
|
|
NM_001291303.3(FAT4):c.9520G>A (p.Val3174Ile)
|
rs2126059556
|
|
NM_001291303.3(FAT4):c.952C>T (p.Gln318Ter)
|
|
|
NM_001291303.3(FAT4):c.953A>G (p.Gln318Arg)
|
|
|
NM_001291303.3(FAT4):c.9583G>A (p.Val3195Ile)
|
|
|
NM_001291303.3(FAT4):c.9585A>G (p.Val3195=)
|
rs750952434
|
|
NM_001291303.3(FAT4):c.9589C>G (p.Leu3197Val)
|
rs763504235
|
|
NM_001291303.3(FAT4):c.9589C>T (p.Leu3197Phe)
|
|
|
NM_001291303.3(FAT4):c.9592T>G (p.Ser3198Ala)
|
|
|
NM_001291303.3(FAT4):c.9600C>G (p.Asp3200Glu)
|
|
|
NM_001291303.3(FAT4):c.9606C>T (p.Phe3202=)
|
rs758295187
|
|
NM_001291303.3(FAT4):c.9612T>C (p.Thr3204=)
|
|
|
NM_001291303.3(FAT4):c.9630A>G (p.Pro3210=)
|
|
|
NM_001291303.3(FAT4):c.9636A>G (p.Gly3212=)
|
|
|
NM_001291303.3(FAT4):c.9648C>T (p.Ile3216=)
|
rs2126059762
|
|
NM_001291303.3(FAT4):c.9655A>C (p.Asn3219His)
|
rs2126059777
|
|
NM_001291303.3(FAT4):c.9656A>G (p.Asn3219Ser)
|
rs2126059779
|
|
NM_001291303.3(FAT4):c.966G>T (p.Thr322=)
|
|
|
NM_001291303.3(FAT4):c.9687T>G (p.Ala3229=)
|
|
|
NM_001291303.3(FAT4):c.9702T>A (p.Thr3234=)
|
rs774988124
|
|
NM_001291303.3(FAT4):c.9703G>A (p.Val3235Ile)
|
|
|
NM_001291303.3(FAT4):c.9704T>A (p.Val3235Glu)
|
|
|
NM_001291303.3(FAT4):c.9711A>G (p.Ser3237=)
|
|
|
NM_001291303.3(FAT4):c.9726C>A (p.Leu3242=)
|
rs1384860308
|
|
NM_001291303.3(FAT4):c.9736G>A (p.Asp3246Asn)
|
|
|
NM_001291303.3(FAT4):c.9740C>T (p.Pro3247Leu)
|
rs2126059908
|
|
NM_001291303.3(FAT4):c.9742A>G (p.Asn3248Asp)
|
rs2126059913
|
|
NM_001291303.3(FAT4):c.9753C>T (p.Val3251=)
|
|
|
NM_001291303.3(FAT4):c.9784A>G (p.Thr3262Ala)
|
rs754811677
|
|
NM_001291303.3(FAT4):c.9806C>G (p.Thr3269Ser)
|
|
|
NM_001291303.3(FAT4):c.9825C>T (p.Val3275=)
|
|
|
NM_001291303.3(FAT4):c.9829G>C (p.Asp3277His)
|
rs775681328
|
|
NM_001291303.3(FAT4):c.9863T>G (p.Ile3288Arg)
|
rs2126060060
|
|
NM_001291303.3(FAT4):c.9864A>G (p.Ile3288Met)
|
|
|
NM_001291303.3(FAT4):c.987C>G (p.Gly329=)
|
rs201547149
|
|
NM_001291303.3(FAT4):c.987C>T (p.Gly329=)
|
rs201547149
|
|
NM_001291303.3(FAT4):c.9881A>G (p.Asn3294Ser)
|
rs2126060089
|
|
NM_001291303.3(FAT4):c.990G>A (p.Val330=)
|
|
|
NM_001291303.3(FAT4):c.9914A>T (p.Tyr3305Phe)
|
|
|
NM_001291303.3(FAT4):c.9927C>A (p.Ile3309=)
|
|
|
NM_001291303.3(FAT4):c.992C>T (p.Pro331Leu)
|
|
|
NM_001291303.3(FAT4):c.9938C>T (p.Ala3313Val)
|
|
|
NM_001291303.3(FAT4):c.9948T>C (p.Gly3316=)
|
|
|
NM_001291303.3(FAT4):c.9952A>G (p.Ile3318Val)
|
|
|
NM_001291303.3(FAT4):c.9953TTG[1] (p.Val3319del)
|
|
|
NM_001291303.3(FAT4):c.9960A>T (p.Gly3320=)
|
|
|
NM_001291303.3(FAT4):c.996C>A (p.Ser332=)
|
|
|
NM_001291303.3(FAT4):c.9973A>G (p.Ser3325Gly)
|
|
|
NM_001291303.3(FAT4):c.9987G>A (p.Leu3329=)
|
|
|
NM_001291303.3(FAT4):c.9988G>T (p.Gly3330Cys)
|
|
|
NM_001291303.3(FAT4):c.9990C>T (p.Gly3330=)
|
rs2126060235
|
|
NM_001291303.3(FAT4):c.9994G>T (p.Asp3332Tyr)
|
|
|