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.8290A>C (p.Asn2764His)
|
rs147281598
|
0.00051
|
NM_001291303.3(FAT4):c.4199G>A (p.Arg1400His)
|
rs376791829
|
0.00047
|
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.6731C>T (p.Thr2244Met)
|
rs145342353
|
0.00030
|
NM_001291303.3(FAT4):c.11378T>C (p.Leu3793Pro)
|
rs149757393
|
0.00023
|
NM_001291303.3(FAT4):c.11380C>T (p.Arg3794Trp)
|
rs201859188
|
0.00020
|
NM_001291303.3(FAT4):c.8812C>A (p.Gln2938Lys)
|
rs370499753
|
0.00019
|
NM_001291303.3(FAT4):c.6977C>T (p.Thr2326Ile)
|
rs200344386
|
0.00017
|
NM_001291303.3(FAT4):c.7079A>G (p.Asn2360Ser)
|
rs534302520
|
0.00017
|
NM_001291303.3(FAT4):c.10643A>G (p.Tyr3548Cys)
|
rs79726583
|
0.00015
|
NM_001291303.3(FAT4):c.5311G>A (p.Ala1771Thr)
|
rs147751409
|
0.00015
|
NM_001291303.3(FAT4):c.13802C>T (p.Pro4601Leu)
|
rs200851934
|
0.00014
|
NM_001291303.3(FAT4):c.1099G>A (p.Val367Ile)
|
rs747531733
|
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.13388C>T (p.Thr4463Ile)
|
rs199971037
|
0.00011
|
NM_001291303.3(FAT4):c.7264A>T (p.Ser2422Cys)
|
rs139924242
|
0.00011
|
NM_001291303.3(FAT4):c.9597T>A (p.Asp3199Glu)
|
rs568003396
|
0.00010
|
NM_001291303.3(FAT4):c.13634C>T (p.Pro4545Leu)
|
rs200092854
|
0.00009
|
NM_001291303.3(FAT4):c.5429A>T (p.Tyr1810Phe)
|
rs201947859
|
0.00009
|
NM_001291303.3(FAT4):c.6976A>G (p.Thr2326Ala)
|
rs757774648
|
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.8636A>G (p.Tyr2879Cys)
|
rs781160819
|
0.00007
|
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.12166G>T (p.Val4056Leu)
|
rs753998777
|
0.00006
|
NM_001291303.3(FAT4):c.1222G>A (p.Glu408Lys)
|
rs574924064
|
0.00006
|
NM_001291303.3(FAT4):c.1289G>A (p.Arg430His)
|
rs774644392
|
0.00006
|
NM_001291303.3(FAT4):c.4706A>G (p.Asn1569Ser)
|
rs768412027
|
0.00006
|
NM_001291303.3(FAT4):c.6917A>G (p.Asn2306Ser)
|
rs369144497
|
0.00006
|
NM_001291303.3(FAT4):c.8408T>C (p.Ile2803Thr)
|
rs745425307
|
0.00006
|
NM_001291303.3(FAT4):c.1811T>G (p.Met604Arg)
|
rs376751408
|
0.00005
|
NM_001291303.3(FAT4):c.8525G>A (p.Arg2842His)
|
rs146180798
|
0.00005
|
NM_001291303.3(FAT4):c.11725A>G (p.Ser3909Gly)
|
rs531337325
|
0.00004
|
NM_001291303.3(FAT4):c.13837G>A (p.Ala4613Thr)
|
rs151087097
|
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.3095C>T (p.Ala1032Val)
|
rs754931963
|
0.00004
|
NM_001291303.3(FAT4):c.4081G>A (p.Gly1361Arg)
|
rs200361960
|
0.00004
|
NM_001291303.3(FAT4):c.548G>A (p.Gly183Glu)
|
rs771566742
|
0.00004
|
NM_001291303.3(FAT4):c.6086C>T (p.Ser2029Phe)
|
rs145573597
|
0.00004
|
NM_001291303.3(FAT4):c.1663C>T (p.Arg555Trp)
|
rs756991867
|
0.00003
|
NM_001291303.3(FAT4):c.458A>G (p.Gln153Arg)
|
rs745934649
|
0.00003
|
NM_001291303.3(FAT4):c.11152C>T (p.Arg3718Cys)
|
rs774217003
|
0.00002
|
NM_001291303.3(FAT4):c.13144G>A (p.Gly4382Arg)
|
rs368409720
|
0.00002
|
NM_001291303.3(FAT4):c.13594A>G (p.Arg4532Gly)
|
rs373502916
|
0.00002
|
NM_001291303.3(FAT4):c.2158A>G (p.Thr720Ala)
|
rs367762836
|
0.00002
|
NM_001291303.3(FAT4):c.4060A>G (p.Ile1354Val)
|
rs200273982
|
0.00002
|
NM_001291303.3(FAT4):c.4274T>G (p.Ile1425Ser)
|
rs759931847
|
0.00002
|
NM_001291303.3(FAT4):c.5645A>G (p.Glu1882Gly)
|
rs757125413
|
0.00002
|
NM_001291303.3(FAT4):c.10868T>C (p.Val3623Ala)
|
rs530781443
|
0.00001
|
NM_001291303.3(FAT4):c.12107G>C (p.Arg4036Thr)
|
rs897405265
|
0.00001
|
NM_001291303.3(FAT4):c.12340A>G (p.Ile4114Val)
|
rs948622582
|
0.00001
|
NM_001291303.3(FAT4):c.132G>C (p.Glu44Asp)
|
rs763601689
|
0.00001
|
NM_001291303.3(FAT4):c.14441G>A (p.Arg4814Lys)
|
rs756452113
|
0.00001
|
NM_001291303.3(FAT4):c.1613G>A (p.Gly538Glu)
|
rs1193758539
|
0.00001
|
NM_001291303.3(FAT4):c.176C>T (p.Thr59Ile)
|
rs757284999
|
0.00001
|
NM_001291303.3(FAT4):c.2641A>G (p.Ile881Val)
|
rs183643556
|
0.00001
|
NM_001291303.3(FAT4):c.2834A>G (p.Lys945Arg)
|
rs1376872414
|
0.00001
|
NM_001291303.3(FAT4):c.3236C>T (p.Pro1079Leu)
|
rs185325824
|
0.00001
|
NM_001291303.3(FAT4):c.5501T>G (p.Val1834Gly)
|
rs748063320
|
0.00001
|
NM_001291303.3(FAT4):c.6109G>A (p.Val2037Ile)
|
rs1192093557
|
0.00001
|
NM_001291303.3(FAT4):c.7516T>G (p.Ser2506Ala)
|
rs148603730
|
0.00001
|
NM_001291303.3(FAT4):c.8216C>A (p.Ser2739Tyr)
|
rs748854090
|
0.00001
|
NM_001291303.3(FAT4):c.10034A>G (p.Lys3345Arg)
|
|
|
NM_001291303.3(FAT4):c.10306A>T (p.Ile3436Phe)
|
|
|
NM_001291303.3(FAT4):c.10338C>G (p.Ile3446Met)
|
|
|
NM_001291303.3(FAT4):c.10379A>C (p.Gln3460Pro)
|
|
|
NM_001291303.3(FAT4):c.10490C>G (p.Ser3497Cys)
|
|
|
NM_001291303.3(FAT4):c.10847C>T (p.Ser3616Phe)
|
|
|
NM_001291303.3(FAT4):c.11219G>C (p.Ser3740Thr)
|
|
|
NM_001291303.3(FAT4):c.11290C>A (p.Leu3764Ile)
|
|
|
NM_001291303.3(FAT4):c.11294T>C (p.Leu3765Ser)
|
|
|
NM_001291303.3(FAT4):c.11296G>T (p.Ala3766Ser)
|
|
|
NM_001291303.3(FAT4):c.11420C>T (p.Ser3807Phe)
|
|
|
NM_001291303.3(FAT4):c.11528A>T (p.Glu3843Val)
|
|
|
NM_001291303.3(FAT4):c.11769C>A (p.Ser3923Arg)
|
|
|
NM_001291303.3(FAT4):c.11831G>A (p.Cys3944Tyr)
|
|
|
NM_001291303.3(FAT4):c.11926G>A (p.Glu3976Lys)
|
|
|
NM_001291303.3(FAT4):c.11945T>G (p.Phe3982Cys)
|
|
|
NM_001291303.3(FAT4):c.11966A>C (p.Glu3989Ala)
|
rs2126076090
|
|
NM_001291303.3(FAT4):c.12043T>C (p.Tyr4015His)
|
|
|
NM_001291303.3(FAT4):c.12131G>A (p.Gly4044Asp)
|
rs760328375
|
|
NM_001291303.3(FAT4):c.12249C>G (p.Asn4083Lys)
|
|
|
NM_001291303.3(FAT4):c.12271G>C (p.Val4091Leu)
|
rs2126082991
|
|
NM_001291303.3(FAT4):c.12301A>T (p.Thr4101Ser)
|
|
|
NM_001291303.3(FAT4):c.12543T>A (p.Asp4181Glu)
|
|
|
NM_001291303.3(FAT4):c.12575A>G (p.Glu4192Gly)
|
|
|
NM_001291303.3(FAT4):c.1262A>C (p.Lys421Thr)
|
|
|
NM_001291303.3(FAT4):c.12676A>C (p.Lys4226Gln)
|
|
|
NM_001291303.3(FAT4):c.12679C>T (p.Arg4227Trp)
|
|
|
NM_001291303.3(FAT4):c.12698A>G (p.Gln4233Arg)
|
|
|
NM_001291303.3(FAT4):c.12812C>T (p.Thr4271Ile)
|
|
|
NM_001291303.3(FAT4):c.13145G>T (p.Gly4382Val)
|
|
|
NM_001291303.3(FAT4):c.13163C>G (p.Ser4388Cys)
|
|
|
NM_001291303.3(FAT4):c.13192A>T (p.Ile4398Phe)
|
|
|
NM_001291303.3(FAT4):c.13606G>A (p.Ala4536Thr)
|
rs1212647138
|
|
NM_001291303.3(FAT4):c.13618A>G (p.Lys4540Glu)
|
|
|
NM_001291303.3(FAT4):c.13673T>C (p.Phe4558Ser)
|
|
|
NM_001291303.3(FAT4):c.13762A>G (p.Arg4588Gly)
|
|
|
NM_001291303.3(FAT4):c.1378A>G (p.Ser460Gly)
|
|
|
NM_001291303.3(FAT4):c.13820T>C (p.Ile4607Thr)
|
|
|
NM_001291303.3(FAT4):c.13934G>A (p.Arg4645His)
|
|
|
NM_001291303.3(FAT4):c.13966C>T (p.His4656Tyr)
|
|
|
NM_001291303.3(FAT4):c.14032C>G (p.Pro4678Ala)
|
|
|
NM_001291303.3(FAT4):c.14033C>A (p.Pro4678His)
|
|
|
NM_001291303.3(FAT4):c.14048G>A (p.Gly4683Asp)
|
|
|
NM_001291303.3(FAT4):c.14089C>G (p.Pro4697Ala)
|
|
|
NM_001291303.3(FAT4):c.14384A>G (p.Glu4795Gly)
|
|
|
NM_001291303.3(FAT4):c.14431G>A (p.Asp4811Asn)
|
|
|
NM_001291303.3(FAT4):c.14479A>G (p.Arg4827Gly)
|
|
|
NM_001291303.3(FAT4):c.1462G>A (p.Ala488Thr)
|
|
|
NM_001291303.3(FAT4):c.14708G>C (p.Gly4903Ala)
|
|
|
NM_001291303.3(FAT4):c.14719A>G (p.Thr4907Ala)
|
rs769212397
|
|
NM_001291303.3(FAT4):c.14815G>T (p.Gly4939Cys)
|
|
|
NM_001291303.3(FAT4):c.1532G>A (p.Arg511His)
|
|
|
NM_001291303.3(FAT4):c.1654A>G (p.Ile552Val)
|
|
|
NM_001291303.3(FAT4):c.1681C>T (p.Pro561Ser)
|
|
|
NM_001291303.3(FAT4):c.1714C>A (p.Leu572Ile)
|
|
|
NM_001291303.3(FAT4):c.172G>A (p.Gly58Ser)
|
|
|
NM_001291303.3(FAT4):c.1827C>A (p.Asp609Glu)
|
rs370300509
|
|
NM_001291303.3(FAT4):c.1855C>A (p.Arg619Ser)
|
|
|
NM_001291303.3(FAT4):c.192C>G (p.Ile64Met)
|
|
|
NM_001291303.3(FAT4):c.1966T>C (p.Ser656Pro)
|
rs1730743959
|
|
NM_001291303.3(FAT4):c.2126C>T (p.Thr709Ile)
|
|
|
NM_001291303.3(FAT4):c.2273C>G (p.Ala758Gly)
|
|
|
NM_001291303.3(FAT4):c.2458A>G (p.Met820Val)
|
|
|
NM_001291303.3(FAT4):c.2462A>G (p.Asp821Gly)
|
|
|
NM_001291303.3(FAT4):c.2494A>G (p.Thr832Ala)
|
|
|
NM_001291303.3(FAT4):c.25A>T (p.Thr9Ser)
|
|
|
NM_001291303.3(FAT4):c.2614A>G (p.Thr872Ala)
|
|
|
NM_001291303.3(FAT4):c.2665A>G (p.Asn889Asp)
|
|
|
NM_001291303.3(FAT4):c.2735T>C (p.Ile912Thr)
|
|
|
NM_001291303.3(FAT4):c.2947A>T (p.Thr983Ser)
|
|
|
NM_001291303.3(FAT4):c.2981C>T (p.Pro994Leu)
|
|
|
NM_001291303.3(FAT4):c.3178C>T (p.Arg1060Cys)
|
|
|
NM_001291303.3(FAT4):c.3288C>A (p.Asn1096Lys)
|
|
|
NM_001291303.3(FAT4):c.3317C>T (p.Thr1106Ile)
|
|
|
NM_001291303.3(FAT4):c.3509G>C (p.Arg1170Thr)
|
|
|
NM_001291303.3(FAT4):c.3577C>G (p.Gln1193Glu)
|
|
|
NM_001291303.3(FAT4):c.3580G>A (p.Ala1194Thr)
|
|
|
NM_001291303.3(FAT4):c.3683A>G (p.Gln1228Arg)
|
|
|
NM_001291303.3(FAT4):c.3809T>C (p.Ile1270Thr)
|
|
|
NM_001291303.3(FAT4):c.3908T>A (p.Ile1303Asn)
|
|
|
NM_001291303.3(FAT4):c.4168A>G (p.Ile1390Val)
|
|
|
NM_001291303.3(FAT4):c.4352T>C (p.Ile1451Thr)
|
|
|
NM_001291303.3(FAT4):c.4413A>G (p.Ile1471Met)
|
rs2125945055
|
|
NM_001291303.3(FAT4):c.4420G>A (p.Val1474Ile)
|
|
|
NM_001291303.3(FAT4):c.4595A>T (p.Gln1532Leu)
|
|
|
NM_001291303.3(FAT4):c.4745G>A (p.Gly1582Glu)
|
rs1553959187
|
|
NM_001291303.3(FAT4):c.4837T>A (p.Ser1613Thr)
|
|
|
NM_001291303.3(FAT4):c.4907C>T (p.Thr1636Ile)
|
|
|
NM_001291303.3(FAT4):c.4937C>T (p.Thr1646Ile)
|
|
|
NM_001291303.3(FAT4):c.5134A>T (p.Ile1712Leu)
|
|
|
NM_001291303.3(FAT4):c.518C>T (p.Ser173Phe)
|
|
|
NM_001291303.3(FAT4):c.5261G>A (p.Gly1754Glu)
|
|
|
NM_001291303.3(FAT4):c.5347G>T (p.Ala1783Ser)
|
|
|
NM_001291303.3(FAT4):c.5419C>T (p.Arg1807Cys)
|
|
|
NM_001291303.3(FAT4):c.5520A>C (p.Lys1840Asn)
|
|
|
NM_001291303.3(FAT4):c.5549T>C (p.Ile1850Thr)
|
|
|
NM_001291303.3(FAT4):c.5884A>T (p.Thr1962Ser)
|
rs749792331
|
|
NM_001291303.3(FAT4):c.5962A>G (p.Ser1988Gly)
|
|
|
NM_001291303.3(FAT4):c.6001A>G (p.Lys2001Glu)
|
|
|
NM_001291303.3(FAT4):c.6066C>G (p.Asp2022Glu)
|
|
|
NM_001291303.3(FAT4):c.6170C>T (p.Thr2057Ile)
|
|
|
NM_001291303.3(FAT4):c.617G>A (p.Gly206Asp)
|
|
|
NM_001291303.3(FAT4):c.6223A>G (p.Thr2075Ala)
|
|
|
NM_001291303.3(FAT4):c.6287A>G (p.Lys2096Arg)
|
|
|
NM_001291303.3(FAT4):c.6424G>T (p.Val2142Phe)
|
|
|
NM_001291303.3(FAT4):c.6448A>G (p.Asn2150Asp)
|
|
|
NM_001291303.3(FAT4):c.6517A>T (p.Ile2173Leu)
|
|
|
NM_001291303.3(FAT4):c.6535G>T (p.Ala2179Ser)
|
|
|
NM_001291303.3(FAT4):c.6637G>T (p.Val2213Phe)
|
|
|
NM_001291303.3(FAT4):c.6640G>T (p.Ala2214Ser)
|
rs149686118
|
|
NM_001291303.3(FAT4):c.6826C>T (p.Pro2276Ser)
|
|
|
NM_001291303.3(FAT4):c.6905G>C (p.Gly2302Ala)
|
rs143204873
|
|
NM_001291303.3(FAT4):c.6946C>G (p.Leu2316Val)
|
|
|
NM_001291303.3(FAT4):c.7018G>C (p.Gly2340Arg)
|
|
|
NM_001291303.3(FAT4):c.7025C>T (p.Pro2342Leu)
|
|
|
NM_001291303.3(FAT4):c.7151T>C (p.Leu2384Ser)
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NM_001291303.3(FAT4):c.7163C>T (p.Ala2388Val)
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NM_001291303.3(FAT4):c.727A>C (p.Ile243Leu)
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NM_001291303.3(FAT4):c.7400G>A (p.Arg2467Lys)
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NM_001291303.3(FAT4):c.7444C>A (p.Leu2482Ile)
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NM_001291303.3(FAT4):c.7451G>A (p.Gly2484Asp)
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NM_001291303.3(FAT4):c.7593C>G (p.Asn2531Lys)
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NM_001291303.3(FAT4):c.772G>C (p.Gly258Arg)
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NM_001291303.3(FAT4):c.7799C>A (p.Pro2600His)
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NM_001291303.3(FAT4):c.785A>G (p.Asp262Gly)
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NM_001291303.3(FAT4):c.7979C>G (p.Thr2660Arg)
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rs761286125
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NM_001291303.3(FAT4):c.8067A>G (p.Ile2689Met)
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NM_001291303.3(FAT4):c.8147A>T (p.Asn2716Ile)
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NM_001291303.3(FAT4):c.8211A>T (p.Lys2737Asn)
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NM_001291303.3(FAT4):c.8444A>G (p.Asp2815Gly)
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rs763149272
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NM_001291303.3(FAT4):c.8450G>T (p.Ser2817Ile)
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NM_001291303.3(FAT4):c.8470C>A (p.Pro2824Thr)
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NM_001291303.3(FAT4):c.8549A>G (p.His2850Arg)
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NM_001291303.3(FAT4):c.8566G>A (p.Val2856Ile)
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NM_001291303.3(FAT4):c.8723A>G (p.Gln2908Arg)
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NM_001291303.3(FAT4):c.8764A>T (p.Ile2922Phe)
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NM_001291303.3(FAT4):c.8862A>G (p.Ile2954Met)
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NM_001291303.3(FAT4):c.8920A>C (p.Asn2974His)
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rs1205109272
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NM_001291303.3(FAT4):c.8962A>C (p.Ser2988Arg)
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NM_001291303.3(FAT4):c.8987A>G (p.Lys2996Arg)
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NM_001291303.3(FAT4):c.9112A>G (p.Asn3038Asp)
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NM_001291303.3(FAT4):c.9358G>T (p.Ala3120Ser)
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NM_001291303.3(FAT4):c.9379A>G (p.Lys3127Glu)
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NM_001291303.3(FAT4):c.9487G>C (p.Glu3163Gln)
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