NM_001291303.3(FAT4):c.3658T>A (p.Ser1220Thr)
|
rs181368820
|
0.00342
|
NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val)
|
rs145639192
|
0.00145
|
NM_001291303.3(FAT4):c.3424G>A (p.Val1142Met)
|
rs202188213
|
0.00140
|
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.11619C>T (p.Cys3873=)
|
rs141328606
|
0.00092
|
NM_001291303.3(FAT4):c.7231A>T (p.Thr2411Ser)
|
rs147297895
|
0.00091
|
NM_001291303.3(FAT4):c.3682C>G (p.Gln1228Glu)
|
rs200227715
|
0.00087
|
NM_001291303.3(FAT4):c.7103C>A (p.Ala2368Glu)
|
rs116568645
|
0.00066
|
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.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.4199G>A (p.Arg1400His)
|
rs376791829
|
0.00047
|
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.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.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.5054G>A (p.Arg1685Gln)
|
rs376422522
|
0.00034
|
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.6731C>T (p.Thr2244Met)
|
rs145342353
|
0.00030
|
NM_001291303.3(FAT4):c.11040G>A (p.Thr3680=)
|
rs147998041
|
0.00026
|
NM_001291303.3(FAT4):c.8078C>T (p.Ser2693Leu)
|
rs148918820
|
0.00025
|
NM_001291303.3(FAT4):c.11378T>C (p.Leu3793Pro)
|
rs149757393
|
0.00023
|
NM_001291303.3(FAT4):c.7196T>C (p.Ile2399Thr)
|
rs140285782
|
0.00023
|
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.12032C>T (p.Ala4011Val)
|
rs149250709
|
0.00019
|
NM_001291303.3(FAT4):c.7798C>T (p.Pro2600Ser)
|
rs146482628
|
0.00019
|
NM_001291303.3(FAT4):c.8821A>G (p.Thr2941Ala)
|
rs151209952
|
0.00019
|
NM_001291303.3(FAT4):c.6977C>T (p.Thr2326Ile)
|
rs200344386
|
0.00017
|
NM_001291303.3(FAT4):c.8731T>C (p.Tyr2911His)
|
rs148655455
|
0.00017
|
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.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.6970C>T (p.Arg2324Trp)
|
rs559079176
|
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.188C>T (p.Thr63Ile)
|
rs754711855
|
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.13193T>C (p.Ile4398Thr)
|
rs200729108
|
0.00012
|
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.6050T>C (p.Val2017Ala)
|
rs188126059
|
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.11198T>C (p.Leu3733Pro)
|
rs145248395
|
0.00010
|
NM_001291303.3(FAT4):c.12778G>A (p.Val4260Ile)
|
rs369024765
|
0.00010
|
NM_001291303.3(FAT4):c.3505C>T (p.Arg1169Trp)
|
rs190175933
|
0.00010
|
NM_001291303.3(FAT4):c.14362G>A (p.Gly4788Arg)
|
rs138173652
|
0.00009
|
NM_001291303.3(FAT4):c.5429A>T (p.Tyr1810Phe)
|
rs201947859
|
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.821C>T (p.Ala274Val)
|
rs199605036
|
0.00009
|
NM_001291303.3(FAT4):c.8537G>A (p.Arg2846Gln)
|
rs373393333
|
0.00009
|
NM_001291303.3(FAT4):c.10994G>C (p.Gly3665Ala)
|
rs777960103
|
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.11462G>A (p.Arg3821Gln)
|
rs142857910
|
0.00007
|
NM_001291303.3(FAT4):c.12358A>G (p.Ile4120Val)
|
rs372543077
|
0.00007
|
NM_001291303.3(FAT4):c.3622C>T (p.Pro1208Ser)
|
rs761868141
|
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.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.12499G>A (p.Ala4167Thr)
|
rs369432764
|
0.00006
|
NM_001291303.3(FAT4):c.1289G>A (p.Arg430His)
|
rs774644392
|
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.2273C>T (p.Ala758Val)
|
rs570502199
|
0.00006
|
NM_001291303.3(FAT4):c.3937C>T (p.Pro1313Ser)
|
rs748743944
|
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.7963G>A (p.Glu2655Lys)
|
rs556536853
|
0.00006
|
NM_001291303.3(FAT4):c.8408T>C (p.Ile2803Thr)
|
rs745425307
|
0.00006
|
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.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.5806G>A (p.Asp1936Asn)
|
rs1235801879
|
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.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.12768C>T (p.Ser4256=)
|
rs1006074076
|
0.00004
|
NM_001291303.3(FAT4):c.13202G>A (p.Arg4401His)
|
rs778549155
|
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.14138C>T (p.Thr4713Met)
|
rs770459923
|
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.2021G>A (p.Arg674His)
|
rs759309740
|
0.00004
|
NM_001291303.3(FAT4):c.2265A>C (p.Glu755Asp)
|
rs377230037
|
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.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.5011C>T (p.Arg1671Cys)
|
rs373116363
|
0.00004
|
NM_001291303.3(FAT4):c.5012G>A (p.Arg1671His)
|
rs375605783
|
0.00004
|
NM_001291303.3(FAT4):c.548G>A (p.Gly183Glu)
|
rs771566742
|
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.6575G>A (p.Gly2192Asp)
|
rs752648220
|
0.00004
|
NM_001291303.3(FAT4):c.9119C>T (p.Thr3040Met)
|
rs778223332
|
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.9695C>T (p.Ala3232Val)
|
rs373873722
|
0.00004
|
NM_001291303.3(FAT4):c.9946G>T (p.Gly3316Cys)
|
rs776046433
|
0.00004
|
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.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.4198C>T (p.Arg1400Cys)
|
rs764898249
|
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.5468C>T (p.Ser1823Leu)
|
rs758045956
|
0.00003
|
NM_001291303.3(FAT4):c.5939C>T (p.Thr1980Ile)
|
rs1458249935
|
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.9494C>T (p.Thr3165Met)
|
rs770333760
|
0.00003
|
NM_001291303.3(FAT4):c.10031G>A (p.Arg3344Gln)
|
rs769028469
|
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.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.13144G>A (p.Gly4382Arg)
|
rs368409720
|
0.00002
|
NM_001291303.3(FAT4):c.13180C>T (p.Pro4394Ser)
|
rs772779154
|
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.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.2158A>G (p.Thr720Ala)
|
rs367762836
|
0.00002
|
NM_001291303.3(FAT4):c.2287A>G (p.Ile763Val)
|
rs774554680
|
0.00002
|
NM_001291303.3(FAT4):c.2382T>G (p.Ser794Arg)
|
rs746206634
|
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.4060A>G (p.Ile1354Val)
|
rs200273982
|
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.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.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.6577A>C (p.Ile2193Leu)
|
rs755984729
|
0.00002
|
NM_001291303.3(FAT4):c.7024C>T (p.Pro2342Ser)
|
rs769744109
|
0.00002
|
NM_001291303.3(FAT4):c.7966A>C (p.Lys2656Gln)
|
rs760398912
|
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.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.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.1012G>A (p.Glu338Lys)
|
rs1452017220
|
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.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.11080A>G (p.Thr3694Ala)
|
rs150752497
|
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.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.11482G>A (p.Val3828Ile)
|
rs773534151
|
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.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.11912T>G (p.Phe3971Cys)
|
rs746181472
|
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.12274A>G (p.Ser4092Gly)
|
rs1326543871
|
0.00001
|
NM_001291303.3(FAT4):c.12286G>A (p.Val4096Ile)
|
rs768534192
|
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.12479+7C>T
|
rs769242691
|
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.12842A>C (p.Tyr4281Ser)
|
rs758804032
|
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.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.14105G>A (p.Arg4702Gln)
|
rs765222973
|
0.00001
|
NM_001291303.3(FAT4):c.14186A>T (p.Asp4729Val)
|
rs372142864
|
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.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.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.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.1882G>A (p.Asp628Asn)
|
rs1730736994
|
0.00001
|
NM_001291303.3(FAT4):c.2057G>A (p.Ser686Asn)
|
rs374104309
|
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.2641A>G (p.Ile881Val)
|
rs183643556
|
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.2896A>G (p.Ile966Val)
|
rs778631726
|
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.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.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.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.4584G>A (p.Met1528Ile)
|
rs1417100834
|
0.00001
|
NM_001291303.3(FAT4):c.473C>G (p.Thr158Ser)
|
rs767365327
|
0.00001
|
NM_001291303.3(FAT4):c.4903A>G (p.Ile1635Val)
|
rs754135078
|
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.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.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.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.6109G>A (p.Val2037Ile)
|
rs1192093557
|
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.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.7516T>G (p.Ser2506Ala)
|
rs148603730
|
0.00001
|
NM_001291303.3(FAT4):c.755G>A (p.Ser252Asn)
|
rs371889798
|
0.00001
|
NM_001291303.3(FAT4):c.7801A>G (p.Met2601Val)
|
rs1578655249
|
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.8216C>A (p.Ser2739Tyr)
|
rs748854090
|
0.00001
|
NM_001291303.3(FAT4):c.8230A>G (p.Thr2744Ala)
|
rs774223392
|
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.8461A>G (p.Thr2821Ala)
|
rs768020749
|
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.8849G>C (p.Arg2950Thr)
|
rs924710061
|
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.9152C>A (p.Ser3051Tyr)
|
rs866162018
|
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.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.9824T>G (p.Val3275Gly)
|
rs1003091170
|
0.00001
|
NC_000004.11:g.(?_126237567)_(126337797_?)dup
|
|
|
NC_000004.11:g.(?_126237567)_(126412923_?)dup
|
|
|
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.10022G>A (p.Gly3341Asp)
|
|
|
NM_001291303.3(FAT4):c.10025A>G (p.Asn3342Ser)
|
|
|
NM_001291303.3(FAT4):c.10070T>C (p.Ile3357Thr)
|
|
|
NM_001291303.3(FAT4):c.10093C>A (p.Arg3365=)
|
rs2126060372
|
|
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.1014G>T (p.Glu338Asp)
|
|
|
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.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.10310C>G (p.Pro3437Arg)
|
|
|
NM_001291303.3(FAT4):c.10336A>T (p.Ile3446Phe)
|
|
|
NM_001291303.3(FAT4):c.10338C>G (p.Ile3446Met)
|
|
|
NM_001291303.3(FAT4):c.10376C>T (p.Pro3459Leu)
|
|
|
NM_001291303.3(FAT4):c.10399A>T (p.Thr3467Ser)
|
|
|
NM_001291303.3(FAT4):c.10451C>G (p.Ala3484Gly)
|
rs2126060831
|
|
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.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.10592C>A (p.Thr3531Asn)
|
rs1726076353
|
|
NM_001291303.3(FAT4):c.10594C>T (p.Leu3532Phe)
|
|
|
NM_001291303.3(FAT4):c.10598A>T (p.Gln3533Leu)
|
|
|
NM_001291303.3(FAT4):c.10615C>A (p.Leu3539Ile)
|
|
|
NM_001291303.3(FAT4):c.10615C>T (p.Leu3539Phe)
|
|
|
NM_001291303.3(FAT4):c.10634C>T (p.Pro3545Leu)
|
|
|
NM_001291303.3(FAT4):c.1063T>A (p.Phe355Ile)
|
rs1471671726
|
|
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.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.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.10769A>T (p.Asp3590Val)
|
|
|
NM_001291303.3(FAT4):c.1076C>T (p.Pro359Leu)
|
|
|
NM_001291303.3(FAT4):c.10788G>A (p.Met3596Ile)
|
rs1447514638
|
|
NM_001291303.3(FAT4):c.10801A>G (p.Thr3601Ala)
|
|
|
NM_001291303.3(FAT4):c.10819A>G (p.Ile3607Val)
|
rs945820499
|
|
NM_001291303.3(FAT4):c.10834A>C (p.Asn3612His)
|
|
|
NM_001291303.3(FAT4):c.10850G>A (p.Arg3617Gln)
|
|
|
NM_001291303.3(FAT4):c.10852A>G (p.Thr3618Ala)
|
rs1726090881
|
|
NM_001291303.3(FAT4):c.1085C>G (p.Ser362Trp)
|
|
|
NM_001291303.3(FAT4):c.10861A>C (p.Ile3621Leu)
|
rs769926658
|
|
NM_001291303.3(FAT4):c.10871A>G (p.Asn3624Ser)
|
|
|
NM_001291303.3(FAT4):c.10894G>A (p.Gly3632Ser)
|
|
|
NM_001291303.3(FAT4):c.10910C>T (p.Ser3637Phe)
|
rs1332535204
|
|
NM_001291303.3(FAT4):c.10936T>G (p.Leu3646Val)
|
|
|
NM_001291303.3(FAT4):c.10957C>T (p.Leu3653Phe)
|
|
|
NM_001291303.3(FAT4):c.11005G>C (p.Asp3669His)
|
rs2126061545
|
|
NM_001291303.3(FAT4):c.11074C>T (p.His3692Tyr)
|
|
|
NM_001291303.3(FAT4):c.11081C>T (p.Thr3694Ile)
|
|
|
NM_001291303.3(FAT4):c.11096T>C (p.Ile3699Thr)
|
|
|
NM_001291303.3(FAT4):c.11123A>G (p.Asn3708Ser)
|
|
|
NM_001291303.3(FAT4):c.11161G>A (p.Val3721Ile)
|
rs557732280
|
|
NM_001291303.3(FAT4):c.11165C>G (p.Pro3722Arg)
|
rs2126061781
|
|
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.11324A>G (p.Tyr3775Cys)
|
rs1341896601
|
|
NM_001291303.3(FAT4):c.11347A>G (p.Thr3783Ala)
|
|
|
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.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.11498A>G (p.Glu3833Gly)
|
|
|
NM_001291303.3(FAT4):c.11517C>G (p.Ile3839Met)
|
|
|
NM_001291303.3(FAT4):c.11531C>T (p.Pro3844Leu)
|
rs142291617
|
|
NM_001291303.3(FAT4):c.11569G>A (p.Ala3857Thr)
|
|
|
NM_001291303.3(FAT4):c.11587A>G (p.Ile3863Val)
|
rs2126062361
|
|
NM_001291303.3(FAT4):c.115T>C (p.Trp39Arg)
|
rs2125938253
|
|
NM_001291303.3(FAT4):c.11639A>G (p.His3880Arg)
|
|
|
NM_001291303.3(FAT4):c.11687G>A (p.Gly3896Asp)
|
|
|
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.11792G>T (p.Gly3931Val)
|
rs777754541
|
|
NM_001291303.3(FAT4):c.11797A>G (p.Thr3933Ala)
|
|
|
NM_001291303.3(FAT4):c.11808G>T (p.Met3936Ile)
|
|
|
NM_001291303.3(FAT4):c.11815T>C (p.Ser3939Pro)
|
|
|
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.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.11900C>A (p.Pro3967Gln)
|
|
|
NM_001291303.3(FAT4):c.11927A>G (p.Glu3976Gly)
|
|
|
NM_001291303.3(FAT4):c.11931G>C (p.Leu3977Phe)
|
|
|
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.11969T>C (p.Phe3990Ser)
|
|
|
NM_001291303.3(FAT4):c.12002A>C (p.Tyr4001Ser)
|
|
|
NM_001291303.3(FAT4):c.12019A>G (p.Ile4007Val)
|
rs913813636
|
|
NM_001291303.3(FAT4):c.12029A>G (p.His4010Arg)
|
|
|
NM_001291303.3(FAT4):c.12067G>A (p.Asp4023Asn)
|
rs372001379
|
|
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.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.12214-3T>C
|
|
|
NM_001291303.3(FAT4):c.12262T>C (p.Tyr4088His)
|
|
|
NM_001291303.3(FAT4):c.12271G>C (p.Val4091Leu)
|
rs2126082991
|
|
NM_001291303.3(FAT4):c.12301A>T (p.Thr4101Ser)
|
|
|
NM_001291303.3(FAT4):c.12310G>A (p.Val4104Ile)
|
rs2126083675
|
|
NM_001291303.3(FAT4):c.12323G>A (p.Arg4108Lys)
|
|
|
NM_001291303.3(FAT4):c.12347C>T (p.Ser4116Phe)
|
rs1560631602
|
|
NM_001291303.3(FAT4):c.12361C>T (p.Leu4121Phe)
|
|
|
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.12416T>C (p.Phe4139Ser)
|
|
|
NM_001291303.3(FAT4):c.12419C>T (p.Ala4140Val)
|
|
|
NM_001291303.3(FAT4):c.12431G>A (p.Arg4144Lys)
|
|
|
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+4T>C
|
rs775906121
|
|
NM_001291303.3(FAT4):c.124G>C (p.Gly42Arg)
|
|
|
NM_001291303.3(FAT4):c.12509G>A (p.Arg4170His)
|
|
|
NM_001291303.3(FAT4):c.12509G>C (p.Arg4170Pro)
|
rs758666028
|
|
NM_001291303.3(FAT4):c.12524A>G (p.His4175Arg)
|
|
|
NM_001291303.3(FAT4):c.12532A>T (p.Thr4178Ser)
|
|
|
NM_001291303.3(FAT4):c.12547T>C (p.Trp4183Arg)
|
|
|
NM_001291303.3(FAT4):c.12559C>G (p.Gln4187Glu)
|
|
|
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.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.12679C>T (p.Arg4227Trp)
|
|
|
NM_001291303.3(FAT4):c.1273G>T (p.Ala425Ser)
|
rs138548779
|
|
NM_001291303.3(FAT4):c.12742C>A (p.Leu4248Met)
|
|
|
NM_001291303.3(FAT4):c.12776G>A (p.Gly4259Asp)
|
|
|
NM_001291303.3(FAT4):c.12781T>G (p.Leu4261Val)
|
|
|
NM_001291303.3(FAT4):c.12806A>G (p.Asn4269Ser)
|
|
|
NM_001291303.3(FAT4):c.12823-10T>C
|
|
|
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.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.13033A>G (p.Ile4345Val)
|
|
|
NM_001291303.3(FAT4):c.13058A>G (p.Asn4353Ser)
|
rs2126093199
|
|
NM_001291303.3(FAT4):c.13075_13076delinsAT (p.Ala4359Ile)
|
|
|
NM_001291303.3(FAT4):c.13097G>T (p.Gly4366Val)
|
|
|
NM_001291303.3(FAT4):c.13113G>T (p.Met4371Ile)
|
|
|
NM_001291303.3(FAT4):c.13169C>T (p.Ser4390Leu)
|
|
|
NM_001291303.3(FAT4):c.13179T>A (p.Asp4393Glu)
|
|
|
NM_001291303.3(FAT4):c.13223G>A (p.Ser4408Asn)
|
rs2126096178
|
|
NM_001291303.3(FAT4):c.13228C>A (p.Pro4410Thr)
|
|
|
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.13310G>A (p.Cys4437Tyr)
|
rs2126096288
|
|
NM_001291303.3(FAT4):c.13372T>C (p.Ser4458Pro)
|
|
|
NM_001291303.3(FAT4):c.1337C>T (p.Ala446Val)
|
|
|
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.13462G>A (p.Gly4488Arg)
|
|
|
NM_001291303.3(FAT4):c.13463G>T (p.Gly4488Val)
|
|
|
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.13544C>A (p.Ala4515Glu)
|
|
|
NM_001291303.3(FAT4):c.13549G>A (p.Val4517Ile)
|
rs142649500
|
|
NM_001291303.3(FAT4):c.13565T>A (p.Val4522Asp)
|
|
|
NM_001291303.3(FAT4):c.13583G>A (p.Cys4528Tyr)
|
rs1560639518
|
|
NM_001291303.3(FAT4):c.13591T>C (p.Cys4531Arg)
|
|
|
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.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.13678G>A (p.Asp4560Asn)
|
rs770945735
|
|
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.13762A>G (p.Arg4588Gly)
|
|
|
NM_001291303.3(FAT4):c.1378A>G (p.Ser460Gly)
|
|
|
NM_001291303.3(FAT4):c.13805A>G (p.His4602Arg)
|
|
|
NM_001291303.3(FAT4):c.1381C>G (p.Leu461Val)
|
|
|
NM_001291303.3(FAT4):c.13827C>G (p.Ser4609Arg)
|
rs767553555
|
|
NM_001291303.3(FAT4):c.13854G>C (p.Glu4618Asp)
|
|
|
NM_001291303.3(FAT4):c.13886G>A (p.Ser4629Asn)
|
|
|
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.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.14086A>G (p.Thr4696Ala)
|
|
|
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.1412A>G (p.His471Arg)
|
|
|
NM_001291303.3(FAT4):c.14144A>G (p.Tyr4715Cys)
|
|
|
NM_001291303.3(FAT4):c.14162G>A (p.Arg4721Lys)
|
|
|
NM_001291303.3(FAT4):c.14167T>A (p.Leu4723Met)
|
rs951647883
|
|
NM_001291303.3(FAT4):c.14185G>A (p.Asp4729Asn)
|
|
|
NM_001291303.3(FAT4):c.1421T>G (p.Val474Gly)
|
|
|
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.14312G>A (p.Arg4771His)
|
|
|
NM_001291303.3(FAT4):c.14324C>T (p.Pro4775Leu)
|
|
|
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.14410A>G (p.Asn4804Asp)
|
|
|
NM_001291303.3(FAT4):c.14462G>A (p.Cys4821Tyr)
|
|
|
NM_001291303.3(FAT4):c.14462G>T (p.Cys4821Phe)
|
rs889999062
|
|
NM_001291303.3(FAT4):c.14465G>T (p.Arg4822Ile)
|
|
|
NM_001291303.3(FAT4):c.14466A>T (p.Arg4822Ser)
|
|
|
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.14516A>T (p.Glu4839Val)
|
|
|
NM_001291303.3(FAT4):c.1451T>A (p.Leu484Gln)
|
|
|
NM_001291303.3(FAT4):c.14547_14550del (p.Phe4850fs)
|
|
|
NM_001291303.3(FAT4):c.14563A>G (p.Met4855Val)
|
rs1560640910
|
|
NM_001291303.3(FAT4):c.14590G>A (p.Val4864Ile)
|
|
|
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.1462G>A (p.Ala488Thr)
|
|
|
NM_001291303.3(FAT4):c.14644G>A (p.Asp4882Asn)
|
|
|
NM_001291303.3(FAT4):c.14667A>T (p.Arg4889Ser)
|
|
|
NM_001291303.3(FAT4):c.14677C>G (p.Arg4893Gly)
|
rs765997899
|
|
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.14786C>T (p.Thr4929Ile)
|
|
|
NM_001291303.3(FAT4):c.14794T>G (p.Trp4932Gly)
|
|
|
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.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.14837T>C (p.Val4946Ala)
|
rs1727651908
|
|
NM_001291303.3(FAT4):c.14841T>A (p.Asp4947Glu)
|
rs768693221
|
|
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.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.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.1588G>A (p.Gly530Ser)
|
|
|
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.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.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.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.1750C>A (p.Gln584Lys)
|
|
|
NM_001291303.3(FAT4):c.1754C>T (p.Pro585Leu)
|
|
|
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.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.1828G>A (p.Gly610Arg)
|
rs374235705
|
|
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.1903G>A (p.Asp635Asn)
|
|
|
NM_001291303.3(FAT4):c.1903G>T (p.Asp635Tyr)
|
rs374308807
|
|
NM_001291303.3(FAT4):c.1934C>T (p.Ser645Phe)
|
rs1730741084
|
|
NM_001291303.3(FAT4):c.1966T>C (p.Ser656Pro)
|
rs1730743959
|
|
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.2074G>C (p.Val692Leu)
|
|
|
NM_001291303.3(FAT4):c.2126C>T (p.Thr709Ile)
|
|
|
NM_001291303.3(FAT4):c.2170G>C (p.Val724Leu)
|
|
|
NM_001291303.3(FAT4):c.2182A>G (p.Ile728Val)
|
|
|
NM_001291303.3(FAT4):c.2200T>C (p.Ser734Pro)
|
rs2125941329
|
|
NM_001291303.3(FAT4):c.2216A>T (p.Asn739Ile)
|
rs200512777
|
|
NM_001291303.3(FAT4):c.2239A>G (p.Thr747Ala)
|
|
|
NM_001291303.3(FAT4):c.2309A>T (p.Asn770Ile)
|
|
|
NM_001291303.3(FAT4):c.2338A>T (p.Thr780Ser)
|
|
|
NM_001291303.3(FAT4):c.234C>A (p.His78Gln)
|
|
|
NM_001291303.3(FAT4):c.2361A>C (p.Gln787His)
|
rs2125941586
|
|
NM_001291303.3(FAT4):c.2416G>A (p.Val806Met)
|
|
|
NM_001291303.3(FAT4):c.2449G>C (p.Ala817Pro)
|
rs1213814030
|
|
NM_001291303.3(FAT4):c.2514G>C (p.Met838Ile)
|
|
|
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.2608G>A (p.Gly870Arg)
|
rs2125941989
|
|
NM_001291303.3(FAT4):c.2611G>T (p.Gly871Cys)
|
|
|
NM_001291303.3(FAT4):c.2614A>G (p.Thr872Ala)
|
|
|
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.2635G>A (p.Val879Ile)
|
|
|
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.2774A>G (p.Asn925Ser)
|
|
|
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.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.2903C>T (p.Ala968Val)
|
rs1390864938
|
|
NM_001291303.3(FAT4):c.2905T>A (p.Ser969Thr)
|
|
|
NM_001291303.3(FAT4):c.2947A>G (p.Thr983Ala)
|
|
|
NM_001291303.3(FAT4):c.2947A>T (p.Thr983Ser)
|
|
|
NM_001291303.3(FAT4):c.2956G>A (p.Val986Ile)
|
|
|
NM_001291303.3(FAT4):c.2965G>A (p.Val989Ile)
|
|
|
NM_001291303.3(FAT4):c.2978C>T (p.Ser993Leu)
|
|
|
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.3022_3023delinsAT (p.Ser1008Ile)
|
|
|
NM_001291303.3(FAT4):c.3028C>T (p.Pro1010Ser)
|
rs771044290
|
|
NM_001291303.3(FAT4):c.3055C>G (p.Gln1019Glu)
|
rs761032436
|
|
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.3136A>G (p.Ile1046Val)
|
|
|
NM_001291303.3(FAT4):c.3138A>G (p.Ile1046Met)
|
|
|
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.3196T>C (p.Tyr1066His)
|
rs374993866
|
|
NM_001291303.3(FAT4):c.3288C>A (p.Asn1096Lys)
|
|
|
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>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.3506G>A (p.Arg1169Gln)
|
|
|
NM_001291303.3(FAT4):c.350A>T (p.Tyr117Phe)
|
|
|
NM_001291303.3(FAT4):c.3515C>T (p.Thr1172Ile)
|
rs535333070
|
|
NM_001291303.3(FAT4):c.3525T>A (p.Phe1175Leu)
|
rs2125943496
|
|
NM_001291303.3(FAT4):c.3538A>G (p.Ile1180Val)
|
|
|
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.3641T>A (p.Phe1214Tyr)
|
rs372590258
|
|
NM_001291303.3(FAT4):c.3647A>G (p.Gln1216Arg)
|
|
|
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.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.3726T>A (p.Asn1242Lys)
|
|
|
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.377G>A (p.Arg126Gln)
|
|
|
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.3808A>C (p.Ile1270Leu)
|
|
|
NM_001291303.3(FAT4):c.3809T>C (p.Ile1270Thr)
|
|
|
NM_001291303.3(FAT4):c.3818T>C (p.Leu1273Ser)
|
rs2125943983
|
|
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.3887A>G (p.Asn1296Ser)
|
|
|
NM_001291303.3(FAT4):c.3893C>T (p.Thr1298Met)
|
|
|
NM_001291303.3(FAT4):c.390C>G (p.Asp130Glu)
|
|
|
NM_001291303.3(FAT4):c.3918A>T (p.Leu1306Phe)
|
rs758711821
|
|
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.3986G>A (p.Arg1329Lys)
|
|
|
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.4027G>A (p.Asp1343Asn)
|
|
|
NM_001291303.3(FAT4):c.4038C>A (p.Asp1346Glu)
|
rs1221303871
|
|
NM_001291303.3(FAT4):c.4040A>G (p.Asn1347Ser)
|
|
|
NM_001291303.3(FAT4):c.4087T>G (p.Phe1363Val)
|
|
|
NM_001291303.3(FAT4):c.4114A>G (p.Ile1372Val)
|
|
|
NM_001291303.3(FAT4):c.4157A>G (p.Tyr1386Cys)
|
|
|
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.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.4249C>A (p.Pro1417Thr)
|
|
|
NM_001291303.3(FAT4):c.428C>T (p.Thr143Ile)
|
|
|
NM_001291303.3(FAT4):c.4375A>G (p.Ile1459Val)
|
|
|
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.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.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.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.4648A>G (p.Ile1550Val)
|
|
|
NM_001291303.3(FAT4):c.4649T>A (p.Ile1550Asn)
|
|
|
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.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.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.4930A>C (p.Ile1644Leu)
|
|
|
NM_001291303.3(FAT4):c.4957G>A (p.Ala1653Thr)
|
|
|
NM_001291303.3(FAT4):c.4966C>A (p.Pro1656Thr)
|
rs1730936860
|
|
NM_001291303.3(FAT4):c.5000T>C (p.Ile1667Thr)
|
rs2125946113
|
|
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.5077G>A (p.Ala1693Thr)
|
|
|
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.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.5230A>G (p.Met1744Val)
|
rs1472593009
|
|
NM_001291303.3(FAT4):c.523C>A (p.Arg175Ser)
|
|
|
NM_001291303.3(FAT4):c.5246T>C (p.Val1749Ala)
|
rs1734278499
|
|
NM_001291303.3(FAT4):c.528C>G (p.Ile176Met)
|
|
|
NM_001291303.3(FAT4):c.5307+6T>A
|
rs910280782
|
|
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.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.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.5416C>T (p.Arg1806Cys)
|
|
|
NM_001291303.3(FAT4):c.5420G>A (p.Arg1807His)
|
|
|
NM_001291303.3(FAT4):c.5431T>G (p.Ser1811Ala)
|
|
|
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.5470G>C (p.Asp1824His)
|
|
|
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.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.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.565A>T (p.Ile189Phe)
|
|
|
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.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.572T>C (p.Leu191Pro)
|
|
|
NM_001291303.3(FAT4):c.5737A>T (p.Ile1913Phe)
|
|
|
NM_001291303.3(FAT4):c.5750G>A (p.Arg1917Gln)
|
|
|
NM_001291303.3(FAT4):c.5760_5761inv (p.Gly1921Ser)
|
|
|
NM_001291303.3(FAT4):c.5767G>A (p.Gly1923Arg)
|
|
|
NM_001291303.3(FAT4):c.5780C>T (p.Thr1927Ile)
|
rs1473579499
|
|
NM_001291303.3(FAT4):c.5786G>T (p.Arg1929Ile)
|
|
|
NM_001291303.3(FAT4):c.5824C>A (p.Pro1942Thr)
|
|
|
NM_001291303.3(FAT4):c.5838G>T (p.Leu1946Phe)
|
|
|
NM_001291303.3(FAT4):c.5849G>A (p.Ser1950Asn)
|
|
|
NM_001291303.3(FAT4):c.5867A>C (p.Asn1956Thr)
|
rs1734726577
|
|
NM_001291303.3(FAT4):c.587A>T (p.Glu196Val)
|
|
|
NM_001291303.3(FAT4):c.5889_5890delinsAA (p.Leu1964Ile)
|
rs2126021497
|
|
NM_001291303.3(FAT4):c.5906C>T (p.Thr1969Ile)
|
|
|
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.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.6092T>C (p.Phe2031Ser)
|
|
|
NM_001291303.3(FAT4):c.613A>G (p.Lys205Glu)
|
|
|
NM_001291303.3(FAT4):c.6148A>G (p.Thr2050Ala)
|
|
|
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.6254T>G (p.Ile2085Ser)
|
|
|
NM_001291303.3(FAT4):c.6262A>T (p.Thr2088Ser)
|
|
|
NM_001291303.3(FAT4):c.629G>T (p.Arg210Leu)
|
rs1353199749
|
|
NM_001291303.3(FAT4):c.6308A>G (p.Asp2103Gly)
|
rs112252276
|
|
NM_001291303.3(FAT4):c.6311G>A (p.Gly2104Asp)
|
|
|
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.6424G>T (p.Val2142Phe)
|
|
|
NM_001291303.3(FAT4):c.6436G>T (p.Asp2146Tyr)
|
|
|
NM_001291303.3(FAT4):c.6491A>G (p.Asn2164Ser)
|
|
|
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.6616T>A (p.Ser2206Thr)
|
|
|
NM_001291303.3(FAT4):c.6638T>C (p.Val2213Ala)
|
|
|
NM_001291303.3(FAT4):c.6640G>T (p.Ala2214Ser)
|
rs149686118
|
|
NM_001291303.3(FAT4):c.6688_6690delinsTTT (p.Gln2230Phe)
|
|
|
NM_001291303.3(FAT4):c.6719C>T (p.Thr2240Ile)
|
rs774192877
|
|
NM_001291303.3(FAT4):c.6721G>T (p.Asp2241Tyr)
|
|
|
NM_001291303.3(FAT4):c.6800A>G (p.Asn2267Ser)
|
|
|
NM_001291303.3(FAT4):c.6815T>C (p.Leu2272Ser)
|
|
|
NM_001291303.3(FAT4):c.6832A>T (p.Thr2278Ser)
|
rs775172064
|
|
NM_001291303.3(FAT4):c.6843+4A>G
|
|
|
NM_001291303.3(FAT4):c.6851C>T (p.Ala2284Val)
|
rs2126028801
|
|
NM_001291303.3(FAT4):c.6866G>A (p.Arg2289Gln)
|
|
|
NM_001291303.3(FAT4):c.6883C>T (p.Leu2295Phe)
|
rs2126028825
|
|
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.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.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.7019-3T>G
|
|
|
NM_001291303.3(FAT4):c.7028C>A (p.Ala2343Asp)
|
|
|
NM_001291303.3(FAT4):c.7028C>T (p.Ala2343Val)
|
|
|
NM_001291303.3(FAT4):c.7060G>T (p.Val2354Leu)
|
|
|
NM_001291303.3(FAT4):c.7103C>T (p.Ala2368Val)
|
rs116568645
|
|
NM_001291303.3(FAT4):c.7132C>T (p.Pro2378Ser)
|
|
|
NM_001291303.3(FAT4):c.7133C>A (p.Pro2378Gln)
|
|
|
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.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.7213G>A (p.Gly2405Ser)
|
|
|
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.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.7382T>A (p.Val2461Asp)
|
|
|
NM_001291303.3(FAT4):c.739C>T (p.Pro247Ser)
|
rs191329848
|
|
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.7466C>A (p.Ala2489Glu)
|
rs144853732
|
|
NM_001291303.3(FAT4):c.7490T>C (p.Ile2497Thr)
|
|
|
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.7577C>T (p.Ala2526Val)
|
|
|
NM_001291303.3(FAT4):c.7593C>G (p.Asn2531Lys)
|
|
|
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.7621C>T (p.His2541Tyr)
|
rs2126056853
|
|
NM_001291303.3(FAT4):c.7628A>C (p.Lys2543Thr)
|
rs2126056866
|
|
NM_001291303.3(FAT4):c.7669A>G (p.Thr2557Ala)
|
|
|
NM_001291303.3(FAT4):c.7681G>A (p.Val2561Met)
|
|
|
NM_001291303.3(FAT4):c.7681G>C (p.Val2561Leu)
|
|
|
NM_001291303.3(FAT4):c.7693G>T (p.Asp2565Tyr)
|
|
|
NM_001291303.3(FAT4):c.7699C>T (p.Pro2567Ser)
|
|
|
NM_001291303.3(FAT4):c.7717G>A (p.Glu2573Lys)
|
rs2126056985
|
|
NM_001291303.3(FAT4):c.7718A>G (p.Glu2573Gly)
|
|
|
NM_001291303.3(FAT4):c.772G>C (p.Gly258Arg)
|
|
|
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.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.7831G>A (p.Gly2611Ser)
|
rs2126057163
|
|
NM_001291303.3(FAT4):c.7837A>G (p.Thr2613Ala)
|
|
|
NM_001291303.3(FAT4):c.7854G>C (p.Gln2618His)
|
|
|
NM_001291303.3(FAT4):c.7915G>T (p.Val2639Leu)
|
|
|
NM_001291303.3(FAT4):c.7949C>T (p.Pro2650Leu)
|
rs2126057386
|
|
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.8008A>G (p.Ile2670Val)
|
|
|
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.8188G>A (p.Val2730Ile)
|
|
|
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.8266A>G (p.Ser2756Gly)
|
|
|
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.8363C>G (p.Pro2788Arg)
|
rs267600011
|
|
NM_001291303.3(FAT4):c.8372A>T (p.Tyr2791Phe)
|
|
|
NM_001291303.3(FAT4):c.8383C>T (p.Arg2795Cys)
|
|
|
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.8518A>C (p.Thr2840Pro)
|
|
|
NM_001291303.3(FAT4):c.8545G>A (p.Ala2849Thr)
|
rs181821271
|
|
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.8686G>A (p.Val2896Ile)
|
|
|
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.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.8836G>A (p.Val2946Met)
|
|
|
NM_001291303.3(FAT4):c.8852A>G (p.His2951Arg)
|
|
|
NM_001291303.3(FAT4):c.8862A>G (p.Ile2954Met)
|
|
|
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.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.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.9087C>A (p.Asn3029Lys)
|
rs201663831
|
|
NM_001291303.3(FAT4):c.9102T>G (p.Phe3034Leu)
|
rs2126059002
|
|
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.914T>C (p.Ile305Thr)
|
|
|
NM_001291303.3(FAT4):c.9200G>A (p.Gly3067Glu)
|
rs867017568
|
|
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.9359C>A (p.Ala3120Glu)
|
|
|
NM_001291303.3(FAT4):c.9362C>T (p.Ala3121Val)
|
|
|
NM_001291303.3(FAT4):c.9390TTC[1] (p.Ser3132del)
|
|
|
NM_001291303.3(FAT4):c.9408A>T (p.Glu3136Asp)
|
|
|
NM_001291303.3(FAT4):c.9425A>G (p.Asn3142Ser)
|
rs2126059432
|
|
NM_001291303.3(FAT4):c.9454A>G (p.Lys3152Glu)
|
rs1308115647
|
|
NM_001291303.3(FAT4):c.9472C>G (p.Leu3158Val)
|
|
|
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.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.953A>G (p.Gln318Arg)
|
|
|
NM_001291303.3(FAT4):c.9583G>A (p.Val3195Ile)
|
|
|
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.9655A>C (p.Asn3219His)
|
rs2126059777
|
|
NM_001291303.3(FAT4):c.9656A>G (p.Asn3219Ser)
|
rs2126059779
|
|
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.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.9784A>G (p.Thr3262Ala)
|
rs754811677
|
|
NM_001291303.3(FAT4):c.9806C>G (p.Thr3269Ser)
|
|
|
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.9881A>G (p.Asn3294Ser)
|
rs2126060089
|
|
NM_001291303.3(FAT4):c.9914A>T (p.Tyr3305Phe)
|
|
|
NM_001291303.3(FAT4):c.992C>T (p.Pro331Leu)
|
|
|
NM_001291303.3(FAT4):c.9938C>T (p.Ala3313Val)
|
|
|
NM_001291303.3(FAT4):c.9952A>G (p.Ile3318Val)
|
|
|
NM_001291303.3(FAT4):c.9953TTG[1] (p.Val3319del)
|
|
|
NM_001291303.3(FAT4):c.9973A>G (p.Ser3325Gly)
|
|
|
NM_001291303.3(FAT4):c.9988G>T (p.Gly3330Cys)
|
|
|
NM_001291303.3(FAT4):c.9994G>T (p.Asp3332Tyr)
|
|
|