NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val)
|
rs145639192
|
0.00145
|
NM_001291303.3(FAT4):c.7103C>A (p.Ala2368Glu)
|
rs116568645
|
0.00066
|
NM_001291303.3(FAT4):c.11260A>G (p.Ser3754Gly)
|
rs79909102
|
0.00061
|
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.12647G>A (p.Arg4216His)
|
rs148170326
|
0.00041
|
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.3049A>G (p.Lys1017Glu)
|
rs200995117
|
0.00029
|
NM_001291303.3(FAT4):c.8078C>T (p.Ser2693Leu)
|
rs148918820
|
0.00025
|
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.8812C>A (p.Gln2938Lys)
|
rs370499753
|
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.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.2897T>C (p.Ile966Thr)
|
rs200952904
|
0.00013
|
NM_001291303.3(FAT4):c.13193T>C (p.Ile4398Thr)
|
rs200729108
|
0.00012
|
NM_001291303.3(FAT4):c.8313T>C (p.Asn2771=)
|
rs148344513
|
0.00012
|
NM_001291303.3(FAT4):c.4080C>T (p.His1360=)
|
rs371821589
|
0.00011
|
NM_001291303.3(FAT4):c.7264A>T (p.Ser2422Cys)
|
rs139924242
|
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.9597T>A (p.Asp3199Glu)
|
rs568003396
|
0.00010
|
NM_001291303.3(FAT4):c.12085G>A (p.Ala4029Thr)
|
rs140544054
|
0.00009
|
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.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.821C>T (p.Ala274Val)
|
rs199605036
|
0.00009
|
NM_001291303.3(FAT4):c.3675T>A (p.Asn1225Lys)
|
rs202235021
|
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.929C>A (p.Pro310His)
|
rs371090730
|
0.00007
|
NM_001291303.3(FAT4):c.12166G>T (p.Val4056Leu)
|
rs753998777
|
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.3067A>G (p.Lys1023Glu)
|
rs758101910
|
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.7582G>A (p.Gly2528Arg)
|
rs199986451
|
0.00006
|
NM_001291303.3(FAT4):c.8408T>C (p.Ile2803Thr)
|
rs745425307
|
0.00006
|
NM_001291303.3(FAT4):c.12910G>A (p.Gly4304Ser)
|
rs746761404
|
0.00005
|
NM_001291303.3(FAT4):c.5806G>A (p.Asp1936Asn)
|
rs1235801879
|
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.10061C>A (p.Thr3354Asn)
|
rs145285004
|
0.00004
|
NM_001291303.3(FAT4):c.1244C>G (p.Pro415Arg)
|
rs746792200
|
0.00004
|
NM_001291303.3(FAT4):c.13837G>A (p.Ala4613Thr)
|
rs151087097
|
0.00004
|
NM_001291303.3(FAT4):c.1420G>A (p.Val474Ile)
|
rs753978592
|
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.5011C>T (p.Arg1671Cys)
|
rs373116363
|
0.00004
|
NM_001291303.3(FAT4):c.5012G>A (p.Arg1671His)
|
rs375605783
|
0.00004
|
NM_001291303.3(FAT4):c.5943T>C (p.Tyr1981=)
|
rs149373164
|
0.00004
|
NM_001291303.3(FAT4):c.5993G>A (p.Gly1998Asp)
|
rs753912480
|
0.00004
|
NM_001291303.3(FAT4):c.9119C>T (p.Thr3040Met)
|
rs778223332
|
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.12406A>G (p.Ile4136Val)
|
rs149985937
|
0.00003
|
NM_001291303.3(FAT4):c.1663C>T (p.Arg555Trp)
|
rs756991867
|
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.5939C>T (p.Thr1980Ile)
|
rs1458249935
|
0.00003
|
NM_001291303.3(FAT4):c.733G>A (p.Asp245Asn)
|
rs563002306
|
0.00003
|
NM_001291303.3(FAT4):c.10227C>T (p.Asn3409=)
|
rs368992969
|
0.00002
|
NM_001291303.3(FAT4):c.10339G>A (p.Gly3447Arg)
|
rs751776479
|
0.00002
|
NM_001291303.3(FAT4):c.11152C>T (p.Arg3718Cys)
|
rs774217003
|
0.00002
|
NM_001291303.3(FAT4):c.11920C>T (p.His3974Tyr)
|
rs776196417
|
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.2382T>G (p.Ser794Arg)
|
rs746206634
|
0.00002
|
NM_001291303.3(FAT4):c.3153A>G (p.Gln1051=)
|
rs372689449
|
0.00002
|
NM_001291303.3(FAT4):c.4417G>A (p.Glu1473Lys)
|
rs377534767
|
0.00002
|
NM_001291303.3(FAT4):c.469G>T (p.Asp157Tyr)
|
rs759072210
|
0.00002
|
NM_001291303.3(FAT4):c.5191C>G (p.Gln1731Glu)
|
rs367948625
|
0.00002
|
NM_001291303.3(FAT4):c.5490T>G (p.Thr1830=)
|
rs1262944393
|
0.00002
|
NM_001291303.3(FAT4):c.7966A>C (p.Lys2656Gln)
|
rs760398912
|
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.1012G>A (p.Glu338Lys)
|
rs1452017220
|
0.00001
|
NM_001291303.3(FAT4):c.10189G>A (p.Val3397Met)
|
rs531437241
|
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.11121C>T (p.Ser3707=)
|
rs747348231
|
0.00001
|
NM_001291303.3(FAT4):c.11134G>T (p.Asp3712Tyr)
|
rs769490380
|
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.12274A>G (p.Ser4092Gly)
|
rs1326543871
|
0.00001
|
NM_001291303.3(FAT4):c.12340A>G (p.Ile4114Val)
|
rs948622582
|
0.00001
|
NM_001291303.3(FAT4):c.13260G>A (p.Gln4420=)
|
rs770683738
|
0.00001
|
NM_001291303.3(FAT4):c.13700A>G (p.Tyr4567Cys)
|
rs772246636
|
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.14433C>G (p.Asp4811Glu)
|
rs368166167
|
0.00001
|
NM_001291303.3(FAT4):c.14701G>A (p.Glu4901Lys)
|
rs746119916
|
0.00001
|
NM_001291303.3(FAT4):c.173G>T (p.Gly58Val)
|
rs749929736
|
0.00001
|
NM_001291303.3(FAT4):c.2204G>A (p.Arg735Gln)
|
rs376468352
|
0.00001
|
NM_001291303.3(FAT4):c.2290G>A (p.Val764Ile)
|
rs746714727
|
0.00001
|
NM_001291303.3(FAT4):c.2824A>G (p.Ile942Val)
|
rs368138514
|
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.3470A>C (p.Asn1157Thr)
|
rs764042588
|
0.00001
|
NM_001291303.3(FAT4):c.3479A>G (p.Gln1160Arg)
|
rs776512346
|
0.00001
|
NM_001291303.3(FAT4):c.4257C>G (p.Ser1419Arg)
|
rs377613970
|
0.00001
|
NM_001291303.3(FAT4):c.44C>G (p.Pro15Arg)
|
rs375956663
|
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.5501T>G (p.Val1834Gly)
|
rs748063320
|
0.00001
|
NM_001291303.3(FAT4):c.6630C>G (p.Ala2210=)
|
rs1049419796
|
0.00001
|
NM_001291303.3(FAT4):c.7088C>T (p.Thr2363Ile)
|
rs780014957
|
0.00001
|
NM_001291303.3(FAT4):c.755G>A (p.Ser252Asn)
|
rs371889798
|
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.8753A>G (p.Glu2918Gly)
|
rs762206992
|
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.9824T>G (p.Val3275Gly)
|
rs1003091170
|
0.00001
|
NM_001291303.3(FAT4):c.10010A>G (p.Tyr3337Cys)
|
|
|
NM_001291303.3(FAT4):c.10028G>A (p.Ser3343Asn)
|
|
|
NM_001291303.3(FAT4):c.10072T>C (p.Tyr3358His)
|
|
|
NM_001291303.3(FAT4):c.1007G>A (p.Arg336His)
|
|
|
NM_001291303.3(FAT4):c.10119G>T (p.Leu3373Phe)
|
|
|
NM_001291303.3(FAT4):c.10182T>A (p.Asn3394Lys)
|
|
|
NM_001291303.3(FAT4):c.10256T>C (p.Val3419Ala)
|
|
|
NM_001291303.3(FAT4):c.10261A>G (p.Ile3421Val)
|
|
|
NM_001291303.3(FAT4):c.10277C>T (p.Thr3426Ile)
|
|
|
NM_001291303.3(FAT4):c.10302C>T (p.Asp3434=)
|
|
|
NM_001291303.3(FAT4):c.10338C>G (p.Ile3446Met)
|
|
|
NM_001291303.3(FAT4):c.10351G>A (p.Glu3451Lys)
|
|
|
NM_001291303.3(FAT4):c.10385G>C (p.Gly3462Ala)
|
|
|
NM_001291303.3(FAT4):c.10483A>G (p.Ser3495Gly)
|
|
|
NM_001291303.3(FAT4):c.10520A>G (p.Asp3507Gly)
|
|
|
NM_001291303.3(FAT4):c.10533G>T (p.Met3511Ile)
|
|
|
NM_001291303.3(FAT4):c.10534C>G (p.Leu3512Val)
|
|
|
NM_001291303.3(FAT4):c.1054G>A (p.Val352Ile)
|
|
|
NM_001291303.3(FAT4):c.10615C>T (p.Leu3539Phe)
|
|
|
NM_001291303.3(FAT4):c.10687A>G (p.Ser3563Gly)
|
|
|
NM_001291303.3(FAT4):c.10699G>A (p.Val3567Ile)
|
|
|
NM_001291303.3(FAT4):c.10706G>C (p.Ser3569Thr)
|
|
|
NM_001291303.3(FAT4):c.10717G>C (p.Glu3573Gln)
|
|
|
NM_001291303.3(FAT4):c.10721T>C (p.Ile3574Thr)
|
|
|
NM_001291303.3(FAT4):c.1074C>A (p.Phe358Leu)
|
|
|
NM_001291303.3(FAT4):c.10763C>T (p.Thr3588Ile)
|
|
|
NM_001291303.3(FAT4):c.10849C>T (p.Arg3617Trp)
|
|
|
NM_001291303.3(FAT4):c.10871A>G (p.Asn3624Ser)
|
|
|
NM_001291303.3(FAT4):c.10900A>G (p.Ile3634Val)
|
|
|
NM_001291303.3(FAT4):c.11074C>T (p.His3692Tyr)
|
|
|
NM_001291303.3(FAT4):c.11219G>C (p.Ser3740Thr)
|
|
|
NM_001291303.3(FAT4):c.11225A>G (p.Gln3742Arg)
|
|
|
NM_001291303.3(FAT4):c.11246C>T (p.Ala3749Val)
|
rs1056083552
|
|
NM_001291303.3(FAT4):c.11258A>G (p.Tyr3753Cys)
|
|
|
NM_001291303.3(FAT4):c.11294T>C (p.Leu3765Ser)
|
|
|
NM_001291303.3(FAT4):c.11347A>G (p.Thr3783Ala)
|
|
|
NM_001291303.3(FAT4):c.11381G>A (p.Arg3794Gln)
|
|
|
NM_001291303.3(FAT4):c.11477G>A (p.Ser3826Asn)
|
|
|
NM_001291303.3(FAT4):c.11481C>T (p.Ser3827=)
|
|
|
NM_001291303.3(FAT4):c.11492G>C (p.Ser3831Thr)
|
|
|
NM_001291303.3(FAT4):c.11494C>T (p.Arg3832Cys)
|
|
|
NM_001291303.3(FAT4):c.11506C>G (p.Pro3836Ala)
|
|
|
NM_001291303.3(FAT4):c.11571G>A (p.Ala3857=)
|
|
|
NM_001291303.3(FAT4):c.11706T>G (p.Asp3902Glu)
|
rs774612831
|
|
NM_001291303.3(FAT4):c.11825A>G (p.Asn3942Ser)
|
|
|
NM_001291303.3(FAT4):c.1184C>A (p.Ser395Tyr)
|
|
|
NM_001291303.3(FAT4):c.11893C>T (p.His3965Tyr)
|
|
|
NM_001291303.3(FAT4):c.11894A>G (p.His3965Arg)
|
|
|
NM_001291303.3(FAT4):c.11927A>G (p.Glu3976Gly)
|
|
|
NM_001291303.3(FAT4):c.11951A>G (p.Glu3984Gly)
|
|
|
NM_001291303.3(FAT4):c.11959T>C (p.Tyr3987His)
|
rs2126076080
|
|
NM_001291303.3(FAT4):c.11965G>C (p.Glu3989Gln)
|
|
|
NM_001291303.3(FAT4):c.12019A>G (p.Ile4007Val)
|
rs913813636
|
|
NM_001291303.3(FAT4):c.12029A>C (p.His4010Pro)
|
|
|
NM_001291303.3(FAT4):c.12097G>A (p.Ala4033Thr)
|
rs1328584807
|
|
NM_001291303.3(FAT4):c.1212G>T (p.Gln404His)
|
|
|
NM_001291303.3(FAT4):c.12139A>C (p.Thr4047Pro)
|
|
|
NM_001291303.3(FAT4):c.12141A>G (p.Thr4047=)
|
|
|
NM_001291303.3(FAT4):c.12155C>T (p.Thr4052Ile)
|
|
|
NM_001291303.3(FAT4):c.12172G>T (p.Asp4058Tyr)
|
|
|
NM_001291303.3(FAT4):c.12323G>A (p.Arg4108Lys)
|
|
|
NM_001291303.3(FAT4):c.12379G>A (p.Val4127Met)
|
|
|
NM_001291303.3(FAT4):c.12389A>C (p.His4130Pro)
|
|
|
NM_001291303.3(FAT4):c.12410T>A (p.Met4137Lys)
|
|
|
NM_001291303.3(FAT4):c.12443C>T (p.Pro4148Leu)
|
|
|
NM_001291303.3(FAT4):c.12478C>G (p.Gln4160Glu)
|
|
|
NM_001291303.3(FAT4):c.12509G>A (p.Arg4170His)
|
|
|
NM_001291303.3(FAT4):c.1253G>C (p.Ser418Thr)
|
|
|
NM_001291303.3(FAT4):c.1256T>C (p.Leu419Pro)
|
|
|
NM_001291303.3(FAT4):c.12682G>C (p.Glu4228Gln)
|
|
|
NM_001291303.3(FAT4):c.1273G>T (p.Ala425Ser)
|
rs138548779
|
|
NM_001291303.3(FAT4):c.12807T>G (p.Asn4269Lys)
|
|
|
NM_001291303.3(FAT4):c.12847A>G (p.Thr4283Ala)
|
|
|
NM_001291303.3(FAT4):c.12874G>A (p.Val4292Met)
|
|
|
NM_001291303.3(FAT4):c.12898T>C (p.Tyr4300His)
|
|
|
NM_001291303.3(FAT4):c.13005G>C (p.Gln4335His)
|
|
|
NM_001291303.3(FAT4):c.13012G>A (p.Gly4338Ser)
|
|
|
NM_001291303.3(FAT4):c.13022A>G (p.Asp4341Gly)
|
|
|
NM_001291303.3(FAT4):c.13035A>G (p.Ile4345Met)
|
|
|
NM_001291303.3(FAT4):c.13090T>G (p.Phe4364Val)
|
|
|
NM_001291303.3(FAT4):c.13091T>A (p.Phe4364Tyr)
|
|
|
NM_001291303.3(FAT4):c.13208C>T (p.Pro4403Leu)
|
|
|
NM_001291303.3(FAT4):c.13213A>G (p.Ile4405Val)
|
|
|
NM_001291303.3(FAT4):c.13214T>C (p.Ile4405Thr)
|
|
|
NM_001291303.3(FAT4):c.13247T>A (p.Leu4416Gln)
|
|
|
NM_001291303.3(FAT4):c.13254T>G (p.Ile4418Met)
|
rs1727561886
|
|
NM_001291303.3(FAT4):c.13282C>T (p.Pro4428Ser)
|
|
|
NM_001291303.3(FAT4):c.1328A>G (p.Asn443Ser)
|
rs1013842967
|
|
NM_001291303.3(FAT4):c.13292A>C (p.Asp4431Ala)
|
|
|
NM_001291303.3(FAT4):c.13305C>T (p.His4435=)
|
rs1357034003
|
|
NM_001291303.3(FAT4):c.13325G>T (p.Ser4442Ile)
|
|
|
NM_001291303.3(FAT4):c.13360A>G (p.Ser4454Gly)
|
|
|
NM_001291303.3(FAT4):c.13367C>A (p.Pro4456Gln)
|
|
|
NM_001291303.3(FAT4):c.13373C>T (p.Ser4458Leu)
|
|
|
NM_001291303.3(FAT4):c.13379C>T (p.Thr4460Met)
|
|
|
NM_001291303.3(FAT4):c.1337C>T (p.Ala446Val)
|
|
|
NM_001291303.3(FAT4):c.13385G>A (p.Arg4462Lys)
|
rs1727568738
|
|
NM_001291303.3(FAT4):c.13391G>A (p.Cys4464Tyr)
|
|
|
NM_001291303.3(FAT4):c.13431G>A (p.Gln4477=)
|
|
|
NM_001291303.3(FAT4):c.13481G>A (p.Ser4494Asn)
|
|
|
NM_001291303.3(FAT4):c.13528A>G (p.Ile4510Val)
|
|
|
NM_001291303.3(FAT4):c.13558C>T (p.Leu4520Phe)
|
|
|
NM_001291303.3(FAT4):c.13762A>G (p.Arg4588Gly)
|
|
|
NM_001291303.3(FAT4):c.1378A>G (p.Ser460Gly)
|
|
|
NM_001291303.3(FAT4):c.13799T>C (p.Ile4600Thr)
|
|
|
NM_001291303.3(FAT4):c.13847A>G (p.Glu4616Gly)
|
|
|
NM_001291303.3(FAT4):c.13880C>A (p.Ala4627Asp)
|
|
|
NM_001291303.3(FAT4):c.13925A>G (p.Lys4642Arg)
|
rs2126097301
|
|
NM_001291303.3(FAT4):c.1392T>A (p.Phe464Leu)
|
|
|
NM_001291303.3(FAT4):c.13961A>G (p.Gln4654Arg)
|
|
|
NM_001291303.3(FAT4):c.14009G>A (p.Gly4670Glu)
|
|
|
NM_001291303.3(FAT4):c.14021T>G (p.Leu4674Trp)
|
|
|
NM_001291303.3(FAT4):c.14120C>A (p.Pro4707His)
|
|
|
NM_001291303.3(FAT4):c.14131TCT[1] (p.Ser4712del)
|
|
|
NM_001291303.3(FAT4):c.14162G>A (p.Arg4721Lys)
|
|
|
NM_001291303.3(FAT4):c.14278G>A (p.Ala4760Thr)
|
|
|
NM_001291303.3(FAT4):c.14312G>A (p.Arg4771His)
|
|
|
NM_001291303.3(FAT4):c.14404C>T (p.Pro4802Ser)
|
rs1727627190
|
|
NM_001291303.3(FAT4):c.14416A>G (p.Ser4806Gly)
|
|
|
NM_001291303.3(FAT4):c.1441A>G (p.Arg481Gly)
|
|
|
NM_001291303.3(FAT4):c.14437G>A (p.Gly4813Arg)
|
|
|
NM_001291303.3(FAT4):c.14465G>T (p.Arg4822Ile)
|
|
|
NM_001291303.3(FAT4):c.14468G>A (p.Arg4823Lys)
|
|
|
NM_001291303.3(FAT4):c.14627A>G (p.Asn4876Ser)
|
|
|
NM_001291303.3(FAT4):c.14652_14653del (p.Asp4884fs)
|
|
|
NM_001291303.3(FAT4):c.14708_14710delinsCAGCACCCAGG (p.Gly4903fs)
|
|
|
NM_001291303.3(FAT4):c.14710C>T (p.Pro4904Ser)
|
|
|
NM_001291303.3(FAT4):c.14756T>C (p.Leu4919Pro)
|
|
|
NM_001291303.3(FAT4):c.1478A>G (p.Tyr493Cys)
|
|
|
NM_001291303.3(FAT4):c.14792A>T (p.Asn4931Ile)
|
|
|
NM_001291303.3(FAT4):c.1480G>T (p.Val494Leu)
|
|
|
NM_001291303.3(FAT4):c.14945_14946del (p.Tyr4982fs)
|
|
|
NM_001291303.3(FAT4):c.1516C>G (p.Leu506Val)
|
|
|
NM_001291303.3(FAT4):c.1539C>G (p.Ser513Arg)
|
|
|
NM_001291303.3(FAT4):c.1561G>C (p.Gly521Arg)
|
|
|
NM_001291303.3(FAT4):c.1624C>T (p.Arg542Cys)
|
|
|
NM_001291303.3(FAT4):c.1633G>C (p.Ala545Pro)
|
|
|
NM_001291303.3(FAT4):c.1703T>A (p.Leu568His)
|
|
|
NM_001291303.3(FAT4):c.1705G>A (p.Val569Ile)
|
rs1730724185
|
|
NM_001291303.3(FAT4):c.172G>A (p.Gly58Ser)
|
|
|
NM_001291303.3(FAT4):c.1754C>T (p.Pro585Leu)
|
|
|
NM_001291303.3(FAT4):c.1765G>C (p.Asp589His)
|
|
|
NM_001291303.3(FAT4):c.1816A>T (p.Arg606Trp)
|
|
|
NM_001291303.3(FAT4):c.1827C>A (p.Asp609Glu)
|
rs370300509
|
|
NM_001291303.3(FAT4):c.1845C>A (p.Asn615Lys)
|
|
|
NM_001291303.3(FAT4):c.1856G>A (p.Arg619His)
|
|
|
NM_001291303.3(FAT4):c.1903G>T (p.Asp635Tyr)
|
rs374308807
|
|
NM_001291303.3(FAT4):c.1915G>A (p.Gly639Arg)
|
|
|
NM_001291303.3(FAT4):c.1934C>T (p.Ser645Phe)
|
rs1730741084
|
|
NM_001291303.3(FAT4):c.1936T>C (p.Ser646Pro)
|
|
|
NM_001291303.3(FAT4):c.1967C>G (p.Ser656Cys)
|
|
|
NM_001291303.3(FAT4):c.1984A>G (p.Thr662Ala)
|
|
|
NM_001291303.3(FAT4):c.200G>T (p.Arg67Leu)
|
|
|
NM_001291303.3(FAT4):c.2021G>T (p.Arg674Leu)
|
rs759309740
|
|
NM_001291303.3(FAT4):c.205G>A (p.Gly69Ser)
|
|
|
NM_001291303.3(FAT4):c.2072C>T (p.Pro691Leu)
|
|
|
NM_001291303.3(FAT4):c.208T>C (p.Phe70Leu)
|
|
|
NM_001291303.3(FAT4):c.2102A>G (p.Asn701Ser)
|
|
|
NM_001291303.3(FAT4):c.2120A>G (p.Tyr707Cys)
|
|
|
NM_001291303.3(FAT4):c.2177A>G (p.Tyr726Cys)
|
|
|
NM_001291303.3(FAT4):c.2186C>A (p.Ser729Tyr)
|
|
|
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>G (p.Asn770Ser)
|
|
|
NM_001291303.3(FAT4):c.230G>A (p.Ser77Asn)
|
|
|
NM_001291303.3(FAT4):c.2332A>G (p.Ile778Val)
|
|
|
NM_001291303.3(FAT4):c.234C>A (p.His78Gln)
|
|
|
NM_001291303.3(FAT4):c.235G>C (p.Ala79Pro)
|
|
|
NM_001291303.3(FAT4):c.235G>T (p.Ala79Ser)
|
|
|
NM_001291303.3(FAT4):c.2390C>T (p.Ala797Val)
|
|
|
NM_001291303.3(FAT4):c.2416G>A (p.Val806Met)
|
|
|
NM_001291303.3(FAT4):c.2422C>A (p.Leu808Met)
|
|
|
NM_001291303.3(FAT4):c.2456C>T (p.Thr819Ile)
|
|
|
NM_001291303.3(FAT4):c.2476A>G (p.Ile826Val)
|
|
|
NM_001291303.3(FAT4):c.2480G>C (p.Ser827Thr)
|
|
|
NM_001291303.3(FAT4):c.2485C>G (p.Leu829Val)
|
|
|
NM_001291303.3(FAT4):c.2486T>G (p.Leu829Arg)
|
|
|
NM_001291303.3(FAT4):c.249A>G (p.Ile83Met)
|
|
|
NM_001291303.3(FAT4):c.2686G>A (p.Ala896Thr)
|
|
|
NM_001291303.3(FAT4):c.2702A>G (p.Asn901Ser)
|
rs2125942162
|
|
NM_001291303.3(FAT4):c.271T>C (p.Tyr91His)
|
|
|
NM_001291303.3(FAT4):c.2726G>A (p.Gly909Asp)
|
|
|
NM_001291303.3(FAT4):c.2731A>G (p.Ser911Gly)
|
|
|
NM_001291303.3(FAT4):c.274A>G (p.Thr92Ala)
|
|
|
NM_001291303.3(FAT4):c.2752G>A (p.Val918Met)
|
|
|
NM_001291303.3(FAT4):c.2787C>T (p.Leu929=)
|
rs1730806684
|
|
NM_001291303.3(FAT4):c.2809A>G (p.Lys937Glu)
|
|
|
NM_001291303.3(FAT4):c.2869G>A (p.Val957Ile)
|
|
|
NM_001291303.3(FAT4):c.2902G>A (p.Ala968Thr)
|
|
|
NM_001291303.3(FAT4):c.2905T>A (p.Ser969Thr)
|
|
|
NM_001291303.3(FAT4):c.2926C>T (p.Leu976Phe)
|
|
|
NM_001291303.3(FAT4):c.2957T>A (p.Val986Asp)
|
|
|
NM_001291303.3(FAT4):c.2990A>G (p.Asp997Gly)
|
|
|
NM_001291303.3(FAT4):c.300C>G (p.Ser100Arg)
|
|
|
NM_001291303.3(FAT4):c.3010A>T (p.Thr1004Ser)
|
|
|
NM_001291303.3(FAT4):c.3028C>T (p.Pro1010Ser)
|
rs771044290
|
|
NM_001291303.3(FAT4):c.3043T>G (p.Phe1015Val)
|
|
|
NM_001291303.3(FAT4):c.3065A>G (p.Asp1022Gly)
|
rs372060616
|
|
NM_001291303.3(FAT4):c.3092T>C (p.Ile1031Thr)
|
|
|
NM_001291303.3(FAT4):c.3151C>A (p.Gln1051Lys)
|
|
|
NM_001291303.3(FAT4):c.3195A>G (p.Arg1065=)
|
|
|
NM_001291303.3(FAT4):c.3199G>A (p.Val1067Ile)
|
|
|
NM_001291303.3(FAT4):c.3202T>G (p.Leu1068Val)
|
|
|
NM_001291303.3(FAT4):c.3286A>G (p.Asn1096Asp)
|
|
|
NM_001291303.3(FAT4):c.3317C>T (p.Thr1106Ile)
|
|
|
NM_001291303.3(FAT4):c.3327C>T (p.Phe1109=)
|
|
|
NM_001291303.3(FAT4):c.3346G>T (p.Gly1116Trp)
|
rs2125943177
|
|
NM_001291303.3(FAT4):c.3408G>T (p.Arg1136Ser)
|
|
|
NM_001291303.3(FAT4):c.3425T>C (p.Val1142Ala)
|
|
|
NM_001291303.3(FAT4):c.3460G>A (p.Glu1154Lys)
|
|
|
NM_001291303.3(FAT4):c.3473C>T (p.Thr1158Ile)
|
|
|
NM_001291303.3(FAT4):c.3494C>G (p.Ser1165Cys)
|
|
|
NM_001291303.3(FAT4):c.3506G>A (p.Arg1169Gln)
|
|
|
NM_001291303.3(FAT4):c.3515C>T (p.Thr1172Ile)
|
rs535333070
|
|
NM_001291303.3(FAT4):c.356C>T (p.Thr119Ile)
|
|
|
NM_001291303.3(FAT4):c.3577C>G (p.Gln1193Glu)
|
|
|
NM_001291303.3(FAT4):c.3643T>C (p.Tyr1215His)
|
|
|
NM_001291303.3(FAT4):c.367G>C (p.Val123Leu)
|
|
|
NM_001291303.3(FAT4):c.3718G>A (p.Gly1240Ser)
|
|
|
NM_001291303.3(FAT4):c.3718G>T (p.Gly1240Cys)
|
|
|
NM_001291303.3(FAT4):c.3748A>T (p.Ile1250Leu)
|
|
|
NM_001291303.3(FAT4):c.3808A>C (p.Ile1270Leu)
|
|
|
NM_001291303.3(FAT4):c.3809T>C (p.Ile1270Thr)
|
|
|
NM_001291303.3(FAT4):c.3842A>G (p.Tyr1281Cys)
|
rs1317645126
|
|
NM_001291303.3(FAT4):c.3873G>T (p.Gly1291=)
|
|
|
NM_001291303.3(FAT4):c.3929A>G (p.Asp1310Gly)
|
|
|
NM_001291303.3(FAT4):c.395C>A (p.Ala132Asp)
|
|
|
NM_001291303.3(FAT4):c.4010T>C (p.Val1337Ala)
|
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NM_001291303.3(FAT4):c.4037A>G (p.Asp1346Gly)
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NM_001291303.3(FAT4):c.4110G>A (p.Gly1370=)
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NM_001291303.3(FAT4):c.4133T>C (p.Leu1378Pro)
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NM_001291303.3(FAT4):c.4143A>T (p.Glu1381Asp)
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NM_001291303.3(FAT4):c.4172C>T (p.Thr1391Ile)
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NM_001291303.3(FAT4):c.418A>G (p.Ile140Val)
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rs1730623781
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NM_001291303.3(FAT4):c.4191A>C (p.Arg1397Ser)
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NM_001291303.3(FAT4):c.4196C>G (p.Pro1399Arg)
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NM_001291303.3(FAT4):c.4210A>G (p.Met1404Val)
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rs779982980
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NM_001291303.3(FAT4):c.4256G>A (p.Ser1419Asn)
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NM_001291303.3(FAT4):c.4285A>G (p.Ile1429Val)
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NM_001291303.3(FAT4):c.4311A>C (p.Thr1437=)
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NM_001291303.3(FAT4):c.4372A>G (p.Thr1458Ala)
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NM_001291303.3(FAT4):c.4378A>G (p.Ile1460Val)
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NM_001291303.3(FAT4):c.4432A>G (p.Ile1478Val)
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rs200565115
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NM_001291303.3(FAT4):c.4447G>C (p.Glu1483Gln)
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NM_001291303.3(FAT4):c.4604T>G (p.Leu1535Arg)
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rs1359875187
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NM_001291303.3(FAT4):c.4621G>T (p.Ala1541Ser)
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NM_001291303.3(FAT4):c.4702A>G (p.Ile1568Val)
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NM_001291303.3(FAT4):c.4705A>C (p.Asn1569His)
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NM_001291303.3(FAT4):c.4707T>G (p.Asn1569Lys)
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NM_001291303.3(FAT4):c.4718A>T (p.Asp1573Val)
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NM_001291303.3(FAT4):c.4721C>T (p.Thr1574Ile)
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NM_001291303.3(FAT4):c.4726A>C (p.Ile1576Leu)
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NM_001291303.3(FAT4):c.4858A>G (p.Ile1620Val)
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NM_001291303.3(FAT4):c.4895C>G (p.Pro1632Arg)
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NM_001291303.3(FAT4):c.4973G>A (p.Gly1658Glu)
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NM_001291303.3(FAT4):c.5039T>A (p.Leu1680His)
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NM_001291303.3(FAT4):c.5098C>G (p.Gln1700Glu)
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NM_001291303.3(FAT4):c.5161A>G (p.Thr1721Ala)
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rs904769252
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NM_001291303.3(FAT4):c.5214A>G (p.Pro1738=)
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NM_001291303.3(FAT4):c.5307+6T>A
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rs910280782
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NM_001291303.3(FAT4):c.5338A>T (p.Ile1780Phe)
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NM_001291303.3(FAT4):c.5355T>G (p.Asp1785Glu)
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rs778606448
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NM_001291303.3(FAT4):c.5368G>A (p.Asp1790Asn)
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NM_001291303.3(FAT4):c.5385T>A (p.Asp1795Glu)
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NM_001291303.3(FAT4):c.5402G>A (p.Arg1801Gln)
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NM_001291303.3(FAT4):c.540T>A (p.Asn180Lys)
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NM_001291303.3(FAT4):c.5420G>T (p.Arg1807Leu)
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NM_001291303.3(FAT4):c.5458C>T (p.Leu1820Phe)
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NM_001291303.3(FAT4):c.5553T>A (p.Pro1851=)
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NM_001291303.3(FAT4):c.5561C>T (p.Thr1854Ile)
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NM_001291303.3(FAT4):c.5569+16C>G
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NM_001291303.3(FAT4):c.5569G>A (p.Gly1857Ser)
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NM_001291303.3(FAT4):c.556C>T (p.Arg186Cys)
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rs577129552
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NM_001291303.3(FAT4):c.5570-4A>G
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NM_001291303.3(FAT4):c.5573C>A (p.Ser1858Tyr)
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NM_001291303.3(FAT4):c.5620G>A (p.Gly1874Arg)
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NM_001291303.3(FAT4):c.5630C>T (p.Thr1877Ile)
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NM_001291303.3(FAT4):c.5722G>T (p.Val1908Leu)
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NM_001291303.3(FAT4):c.5801T>C (p.Ile1934Thr)
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NM_001291303.3(FAT4):c.5880A>T (p.Gly1960=)
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rs756664489
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NM_001291303.3(FAT4):c.5889_5890delinsAA (p.Leu1964Ile)
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rs2126021497
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NM_001291303.3(FAT4):c.5906C>T (p.Thr1969Ile)
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NM_001291303.3(FAT4):c.5914G>A (p.Asp1972Asn)
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NM_001291303.3(FAT4):c.5927A>G (p.Asn1976Ser)
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NM_001291303.3(FAT4):c.593C>T (p.Ala198Val)
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NM_001291303.3(FAT4):c.5944A>G (p.Ser1982Gly)
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rs746510253
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NM_001291303.3(FAT4):c.5950G>A (p.Ala1984Thr)
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NM_001291303.3(FAT4):c.5955A>C (p.Ser1985=)
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NM_001291303.3(FAT4):c.5A>G (p.Asp2Gly)
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NM_001291303.3(FAT4):c.6028A>G (p.Ser2010Gly)
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NM_001291303.3(FAT4):c.6077T>G (p.Ile2026Ser)
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NM_001291303.3(FAT4):c.6079C>T (p.Pro2027Ser)
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NM_001291303.3(FAT4):c.6099C>T (p.Ser2033=)
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rs1734990759
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NM_001291303.3(FAT4):c.6122T>C (p.Leu2041Ser)
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NM_001291303.3(FAT4):c.6146C>T (p.Pro2049Leu)
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NM_001291303.3(FAT4):c.614A>C (p.Lys205Thr)
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NM_001291303.3(FAT4):c.61G>C (p.Val21Leu)
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NM_001291303.3(FAT4):c.6217C>G (p.Gln2073Glu)
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NM_001291303.3(FAT4):c.6260A>G (p.Tyr2087Cys)
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NM_001291303.3(FAT4):c.6302C>T (p.Thr2101Ile)
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NM_001291303.3(FAT4):c.6394C>A (p.Pro2132Thr)
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NM_001291303.3(FAT4):c.6404C>T (p.Ser2135Phe)
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NM_001291303.3(FAT4):c.6433C>G (p.Leu2145Val)
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NM_001291303.3(FAT4):c.6443A>G (p.Asn2148Ser)
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NM_001291303.3(FAT4):c.6515A>C (p.Asp2172Ala)
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rs1328569048
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NM_001291303.3(FAT4):c.6554C>A (p.Thr2185Lys)
|
rs1553968839
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NM_001291303.3(FAT4):c.6568C>T (p.Arg2190Cys)
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NM_001291303.3(FAT4):c.6580G>A (p.Val2194Ile)
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NM_001291303.3(FAT4):c.6586G>T (p.Gly2196Cys)
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NM_001291303.3(FAT4):c.6635C>G (p.Thr2212Ser)
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NM_001291303.3(FAT4):c.6657A>G (p.Arg2219=)
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NM_001291303.3(FAT4):c.665T>A (p.Val222Glu)
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NM_001291303.3(FAT4):c.6667C>T (p.Pro2223Ser)
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NM_001291303.3(FAT4):c.6737G>A (p.Ser2246Asn)
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NM_001291303.3(FAT4):c.6772G>A (p.Val2258Ile)
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NM_001291303.3(FAT4):c.6810G>A (p.Glu2270=)
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NM_001291303.3(FAT4):c.6826C>T (p.Pro2276Ser)
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NM_001291303.3(FAT4):c.6830G>A (p.Arg2277Lys)
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NM_001291303.3(FAT4):c.6843+4A>G
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NM_001291303.3(FAT4):c.6843+9A>G
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NM_001291303.3(FAT4):c.6905G>A (p.Gly2302Asp)
|
rs143204873
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NM_001291303.3(FAT4):c.6937A>G (p.Ser2313Gly)
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NM_001291303.3(FAT4):c.6958C>G (p.Gln2320Glu)
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NM_001291303.3(FAT4):c.697T>C (p.Tyr233His)
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NM_001291303.3(FAT4):c.6986G>A (p.Arg2329His)
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NM_001291303.3(FAT4):c.698A>T (p.Tyr233Phe)
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NM_001291303.3(FAT4):c.7018+5G>T
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NM_001291303.3(FAT4):c.7046C>A (p.Thr2349Lys)
|
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NM_001291303.3(FAT4):c.7054G>A (p.Val2352Ile)
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|
NM_001291303.3(FAT4):c.7088C>G (p.Thr2363Arg)
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NM_001291303.3(FAT4):c.7093G>T (p.Ala2365Ser)
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NM_001291303.3(FAT4):c.7136C>T (p.Thr2379Ile)
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|
NM_001291303.3(FAT4):c.7140A>T (p.Gly2380=)
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NM_001291303.3(FAT4):c.7151T>C (p.Leu2384Ser)
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NM_001291303.3(FAT4):c.7155G>T (p.Leu2385Phe)
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|
NM_001291303.3(FAT4):c.7162G>T (p.Ala2388Ser)
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NM_001291303.3(FAT4):c.7213G>A (p.Gly2405Ser)
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NM_001291303.3(FAT4):c.7267G>A (p.Ala2423Thr)
|
rs776977766
|
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NM_001291303.3(FAT4):c.7283A>G (p.Glu2428Gly)
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NM_001291303.3(FAT4):c.7325C>T (p.Ala2442Val)
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NM_001291303.3(FAT4):c.7348A>G (p.Ser2450Gly)
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NM_001291303.3(FAT4):c.7466C>A (p.Ala2489Glu)
|
rs144853732
|
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NM_001291303.3(FAT4):c.7502C>T (p.Ser2501Phe)
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NM_001291303.3(FAT4):c.7504G>A (p.Glu2502Lys)
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NM_001291303.3(FAT4):c.7555C>G (p.Pro2519Ala)
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NM_001291303.3(FAT4):c.7747C>T (p.Pro2583Ser)
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NM_001291303.3(FAT4):c.7757C>A (p.Ser2586Tyr)
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NM_001291303.3(FAT4):c.7847T>C (p.Ile2616Thr)
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|
NM_001291303.3(FAT4):c.7883C>T (p.Pro2628Leu)
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NM_001291303.3(FAT4):c.7891T>C (p.Phe2631Leu)
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|
NM_001291303.3(FAT4):c.7903C>A (p.Gln2635Lys)
|
|
|
NM_001291303.3(FAT4):c.7908A>G (p.Lys2636=)
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|
NM_001291303.3(FAT4):c.7939G>T (p.Gly2647Cys)
|
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|
NM_001291303.3(FAT4):c.7972G>T (p.Asp2658Tyr)
|
|
|
NM_001291303.3(FAT4):c.7979C>G (p.Thr2660Arg)
|
rs761286125
|
|
NM_001291303.3(FAT4):c.8060G>A (p.Arg2687Gln)
|
|
|
NM_001291303.3(FAT4):c.8062A>G (p.Lys2688Glu)
|
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|
NM_001291303.3(FAT4):c.8134G>A (p.Gly2712Ser)
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|
NM_001291303.3(FAT4):c.8155A>C (p.Ser2719Arg)
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|
NM_001291303.3(FAT4):c.8158A>G (p.Ile2720Val)
|
|
|
NM_001291303.3(FAT4):c.8183G>A (p.Arg2728Lys)
|
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|
NM_001291303.3(FAT4):c.8188G>A (p.Val2730Ile)
|
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|
NM_001291303.3(FAT4):c.818C>T (p.Ala273Val)
|
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|
NM_001291303.3(FAT4):c.8351C>G (p.Pro2784Arg)
|
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|
NM_001291303.3(FAT4):c.8407A>G (p.Ile2803Val)
|
|
|
NM_001291303.3(FAT4):c.842C>A (p.Thr281Asn)
|
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|
NM_001291303.3(FAT4):c.8549A>G (p.His2850Arg)
|
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|
NM_001291303.3(FAT4):c.857G>T (p.Arg286Leu)
|
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|
NM_001291303.3(FAT4):c.8617A>G (p.Arg2873Gly)
|
|
|
NM_001291303.3(FAT4):c.8654A>C (p.Glu2885Ala)
|
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|
NM_001291303.3(FAT4):c.8666T>C (p.Ile2889Thr)
|
|
|
NM_001291303.3(FAT4):c.8751A>T (p.Ser2917=)
|
|
|
NM_001291303.3(FAT4):c.8774C>T (p.Thr2925Ile)
|
|
|
NM_001291303.3(FAT4):c.877G>A (p.Gly293Arg)
|
|
|
NM_001291303.3(FAT4):c.884C>T (p.Pro295Leu)
|
|
|
NM_001291303.3(FAT4):c.8862A>G (p.Ile2954Met)
|
|
|
NM_001291303.3(FAT4):c.8881G>A (p.Gly2961Ser)
|
|
|
NM_001291303.3(FAT4):c.8909C>T (p.Thr2970Ile)
|
|
|
NM_001291303.3(FAT4):c.8920A>G (p.Asn2974Asp)
|
|
|
NM_001291303.3(FAT4):c.8921A>G (p.Asn2974Ser)
|
|
|
NM_001291303.3(FAT4):c.8968T>G (p.Tyr2990Asp)
|
|
|
NM_001291303.3(FAT4):c.9026C>T (p.Ala3009Val)
|
|
|
NM_001291303.3(FAT4):c.9040G>C (p.Asp3014His)
|
|
|
NM_001291303.3(FAT4):c.9092T>C (p.Leu3031Ser)
|
|
|
NM_001291303.3(FAT4):c.9104A>G (p.Lys3035Arg)
|
|
|
NM_001291303.3(FAT4):c.9110A>G (p.Asp3037Gly)
|
|
|
NM_001291303.3(FAT4):c.9122G>A (p.Gly3041Glu)
|
|
|
NM_001291303.3(FAT4):c.9145C>A (p.Leu3049Met)
|
|
|
NM_001291303.3(FAT4):c.9161A>T (p.Asn3054Ile)
|
|
|
NM_001291303.3(FAT4):c.9184A>G (p.Thr3062Ala)
|
|
|
NM_001291303.3(FAT4):c.9203A>G (p.Asn3068Ser)
|
|
|
NM_001291303.3(FAT4):c.9224C>T (p.Ala3075Val)
|
|
|
NM_001291303.3(FAT4):c.9309C>G (p.Ser3103Arg)
|
|
|
NM_001291303.3(FAT4):c.9325A>G (p.Ile3109Val)
|
|
|
NM_001291303.3(FAT4):c.9379A>G (p.Lys3127Glu)
|
|
|
NM_001291303.3(FAT4):c.9413T>A (p.Ile3138Asn)
|
|
|
NM_001291303.3(FAT4):c.9487G>A (p.Glu3163Lys)
|
|
|
NM_001291303.3(FAT4):c.9505A>G (p.Ile3169Val)
|
|
|
NM_001291303.3(FAT4):c.9517T>G (p.Trp3173Gly)
|
|
|
NM_001291303.3(FAT4):c.954A>T (p.Gln318His)
|
|
|
NM_001291303.3(FAT4):c.9571G>A (p.Asp3191Asn)
|
|
|
NM_001291303.3(FAT4):c.9640A>G (p.Thr3214Ala)
|
|
|
NM_001291303.3(FAT4):c.965C>T (p.Thr322Met)
|
|
|
NM_001291303.3(FAT4):c.9709T>C (p.Ser3237Pro)
|
|
|
NM_001291303.3(FAT4):c.9727T>C (p.Phe3243Leu)
|
|
|
NM_001291303.3(FAT4):c.9821A>G (p.Asn3274Ser)
|
|
|
NM_001291303.3(FAT4):c.9838A>T (p.Arg3280Trp)
|
|
|
NM_001291303.3(FAT4):c.9853A>G (p.Thr3285Ala)
|
|
|
NM_001291303.3(FAT4):c.9953T>A (p.Ile3318Asn)
|
|
|
NM_001291303.3(FAT4):c.995C>T (p.Ser332Phe)
|
|
|
NM_001291303.3(FAT4):c.9964G>A (p.Val3322Met)
|
|
|
NM_001291303.3(FAT4):c.9971C>T (p.Ala3324Val)
|
|
|
NM_001291303.3(FAT4):c.9973A>G (p.Ser3325Gly)
|
|
|
NM_001291303.3(FAT4):c.9988G>T (p.Gly3330Cys)
|
|
|