NM_000487.6(ARSA):c.656G>A (p.Arg219His)
|
rs148403406
|
0.00021
|
NM_000487.6(ARSA):c.605G>A (p.Arg202His)
|
rs201794808
|
0.00019
|
NM_000487.6(ARSA):c.680C>G (p.Ser227Cys)
|
rs138468395
|
0.00019
|
NM_000487.6(ARSA):c.14C>T (p.Ala5Val)
|
rs201315540
|
0.00018
|
NM_000487.6(ARSA):c.1258A>C (p.Ser420Arg)
|
rs139073195
|
0.00013
|
NM_000487.6(ARSA):c.728G>A (p.Arg243His)
|
rs142142638
|
0.00008
|
NM_000487.6(ARSA):c.1334G>T (p.Gly445Val)
|
rs540762357
|
0.00007
|
NM_000487.6(ARSA):c.637G>A (p.Asp213Asn)
|
rs369786038
|
0.00006
|
NM_000487.6(ARSA):c.825G>T (p.Glu275Asp)
|
rs907795869
|
0.00006
|
NM_000487.6(ARSA):c.325G>A (p.Val109Met)
|
rs746259972
|
0.00004
|
NM_000487.6(ARSA):c.492C>G (p.Phe164Leu)
|
rs745605987
|
0.00004
|
NM_000487.6(ARSA):c.601G>T (p.Ala201Ser)
|
rs377625311
|
0.00004
|
NM_000487.6(ARSA):c.1157G>A (p.Arg386His)
|
rs747155690
|
0.00003
|
NM_000487.6(ARSA):c.13G>A (p.Ala5Thr)
|
rs765893073
|
0.00003
|
NM_000487.6(ARSA):c.1441C>T (p.Arg481Trp)
|
rs747443475
|
0.00003
|
NM_000487.6(ARSA):c.1442G>A (p.Arg481Gln)
|
rs776116011
|
0.00003
|
NM_000487.6(ARSA):c.1444G>A (p.Gly482Ser)
|
rs377717242
|
0.00003
|
NM_000487.6(ARSA):c.229G>T (p.Ala77Ser)
|
rs763880042
|
0.00003
|
NM_000487.6(ARSA):c.470C>T (p.Pro157Leu)
|
rs74315464
|
0.00003
|
NM_000487.6(ARSA):c.514G>A (p.Gly172Ser)
|
rs74315271
|
0.00003
|
NM_000487.6(ARSA):c.902G>A (p.Arg301Gln)
|
rs573456864
|
0.00003
|
NM_000487.6(ARSA):c.1450G>C (p.Asp484His)
|
rs749061034
|
0.00002
|
NM_000487.6(ARSA):c.1489C>T (p.Pro497Ser)
|
rs1250959266
|
0.00002
|
NM_000487.6(ARSA):c.343G>A (p.Ala115Thr)
|
rs1421381874
|
0.00002
|
NM_000487.6(ARSA):c.592G>A (p.Gly198Arg)
|
rs144393886
|
0.00002
|
NM_000487.6(ARSA):c.604C>T (p.Arg202Cys)
|
rs374482942
|
0.00002
|
NM_000487.6(ARSA):c.629T>A (p.Leu210His)
|
rs762593908
|
0.00002
|
NM_000487.6(ARSA):c.684C>T (p.His228=)
|
rs762695598
|
0.00002
|
NM_000487.6(ARSA):c.855-3C>T
|
rs1338786023
|
0.00002
|
NM_000487.6(ARSA):c.1063T>G (p.Leu355Val)
|
rs763446964
|
0.00001
|
NM_000487.6(ARSA):c.1106A>C (p.Lys369Thr)
|
rs200901626
|
0.00001
|
NM_000487.6(ARSA):c.1211-5C>G
|
rs778131215
|
0.00001
|
NM_000487.6(ARSA):c.1277A>G (p.Glu426Gly)
|
rs376220189
|
0.00001
|
NM_000487.6(ARSA):c.131C>T (p.Pro44Leu)
|
rs1340814173
|
0.00001
|
NM_000487.6(ARSA):c.1321T>G (p.Tyr441Asp)
|
rs2082645489
|
0.00001
|
NM_000487.6(ARSA):c.134G>C (p.Ser45Thr)
|
rs867624246
|
0.00001
|
NM_000487.6(ARSA):c.135C>A (p.Ser45Arg)
|
rs375493957
|
0.00001
|
NM_000487.6(ARSA):c.1415T>C (p.Val472Ala)
|
rs978574508
|
0.00001
|
NM_000487.6(ARSA):c.1423G>A (p.Gly475Ser)
|
rs1017776709
|
0.00001
|
NM_000487.6(ARSA):c.1445G>A (p.Gly482Asp)
|
rs745438306
|
0.00001
|
NM_000487.6(ARSA):c.1522C>T (p.His508Tyr)
|
rs1278738755
|
0.00001
|
NM_000487.6(ARSA):c.242G>C (p.Gly81Ala)
|
rs1389990700
|
0.00001
|
NM_000487.6(ARSA):c.25C>T (p.Leu9Phe)
|
rs886057658
|
0.00001
|
NM_000487.6(ARSA):c.350G>A (p.Gly117Asp)
|
rs1433109241
|
0.00001
|
NM_000487.6(ARSA):c.499G>T (p.Ala167Ser)
|
rs578188411
|
0.00001
|
NM_000487.6(ARSA):c.56T>C (p.Val19Ala)
|
rs1235007867
|
0.00001
|
NM_000487.6(ARSA):c.610A>G (p.Met204Val)
|
rs1569080377
|
0.00001
|
NM_000487.6(ARSA):c.727C>T (p.Arg243Cys)
|
rs369593442
|
0.00001
|
NM_000487.6(ARSA):c.867G>A (p.Met289Ile)
|
rs761919002
|
0.00001
|
NM_000487.6(ARSA):c.878G>A (p.Arg293Gln)
|
rs373866455
|
0.00001
|
NM_000487.6(ARSA):c.970A>G (p.Ile324Val)
|
rs557527090
|
0.00001
|
NM_000487.6(ARSA):c.971T>C (p.Ile324Thr)
|
rs1338627220
|
0.00001
|
NM_000487.6(ARSA):c.1012C>G (p.Leu338Val)
|
rs2146719624
|
|
NM_000487.6(ARSA):c.1030G>C (p.Ala344Pro)
|
|
|
NM_000487.6(ARSA):c.104A>G (p.Tyr35Cys)
|
rs74315268
|
|
NM_000487.6(ARSA):c.104A>T (p.Tyr35Phe)
|
|
|
NM_000487.6(ARSA):c.1052C>T (p.Pro351Leu)
|
|
|
NM_000487.6(ARSA):c.10G>A (p.Gly4Arg)
|
|
|
NM_000487.6(ARSA):c.1107G>C (p.Lys369Asn)
|
rs199476369
|
|
NM_000487.6(ARSA):c.1108-12C>G
|
rs757806374
|
|
NM_000487.6(ARSA):c.1118A>C (p.Gln373Pro)
|
|
|
NM_000487.6(ARSA):c.1149C>A (p.Asp383Glu)
|
|
|
NM_000487.6(ARSA):c.1157G>C (p.Arg386Pro)
|
rs747155690
|
|
NM_000487.6(ARSA):c.1162G>T (p.Val388Phe)
|
rs1222719732
|
|
NM_000487.6(ARSA):c.116G>A (p.Gly39Asp)
|
|
|
NM_000487.6(ARSA):c.1171G>C (p.Val391Leu)
|
|
|
NM_000487.6(ARSA):c.1177_1178delinsGG (p.Thr393Gly)
|
rs2146717703
|
|
NM_000487.6(ARSA):c.1211-2A>G
|
rs74925710
|
|
NM_000487.6(ARSA):c.1211-3C>T
|
|
|
NM_000487.6(ARSA):c.1252G>A (p.Ala418Thr)
|
|
|
NM_000487.6(ARSA):c.1256C>A (p.Ser419Tyr)
|
rs998702737
|
|
NM_000487.6(ARSA):c.1280C>T (p.Pro427Leu)
|
|
|
NM_000487.6(ARSA):c.1294G>A (p.Asp432Asn)
|
|
|
NM_000487.6(ARSA):c.1298T>G (p.Leu433Arg)
|
rs2146716505
|
|
NM_000487.6(ARSA):c.1305G>A (p.Lys435=)
|
rs2146716483
|
|
NM_000487.6(ARSA):c.130C>A (p.Pro44Thr)
|
|
|
NM_000487.6(ARSA):c.1313G>A (p.Gly438Asp)
|
|
|
NM_000487.6(ARSA):c.1341G>A (p.Val447=)
|
|
|
NM_000487.6(ARSA):c.1363C>A (p.Leu455Met)
|
|
|
NM_000487.6(ARSA):c.1370C>T (p.Ala457Val)
|
|
|
NM_000487.6(ARSA):c.1376A>G (p.Lys459Arg)
|
|
|
NM_000487.6(ARSA):c.1385A>G (p.Gln462Arg)
|
rs2146716052
|
|
NM_000487.6(ARSA):c.1390C>T (p.Leu464Phe)
|
rs2146716030
|
|
NM_000487.6(ARSA):c.1397C>T (p.Ala466Val)
|
rs763065602
|
|
NM_000487.6(ARSA):c.1408_1419del (p.Ala470_Thr473del)
|
rs2082643081
|
|
NM_000487.6(ARSA):c.1417A>T (p.Thr473Ser)
|
rs1603444852
|
|
NM_000487.6(ARSA):c.1429A>T (p.Ser477Cys)
|
|
|
NM_000487.6(ARSA):c.1434G>C (p.Gln478His)
|
rs769169905
|
|
NM_000487.6(ARSA):c.1435G>A (p.Val479Met)
|
|
|
NM_000487.6(ARSA):c.1436T>C (p.Val479Ala)
|
|
|
NM_000487.6(ARSA):c.1439C>T (p.Ala480Val)
|
rs1490565534
|
|
NM_000487.6(ARSA):c.1446C>T (p.Gly482=)
|
rs759357711
|
|
NM_000487.6(ARSA):c.1453C>T (p.Pro485Ser)
|
|
|
NM_000487.6(ARSA):c.1456G>A (p.Ala486Thr)
|
|
|
NM_000487.6(ARSA):c.1463A>G (p.Gln488Arg)
|
rs2146715572
|
|
NM_000487.6(ARSA):c.1472G>A (p.Cys491Tyr)
|
rs1060499585
|
|
NM_000487.6(ARSA):c.1480G>A (p.Gly494Ser)
|
rs144323513
|
|
NM_000487.6(ARSA):c.1492C>A (p.Arg498Ser)
|
|
|
NM_000487.6(ARSA):c.1492C>T (p.Arg498Cys)
|
|
|
NM_000487.6(ARSA):c.1492del (p.Arg498fs)
|
|
|
NM_000487.6(ARSA):c.1516G>T (p.Asp506Tyr)
|
rs764345345
|
|
NM_000487.6(ARSA):c.151C>G (p.Leu51Val)
|
rs1348625953
|
|
NM_000487.6(ARSA):c.1523A>G (p.His508Arg)
|
rs2082640761
|
|
NM_000487.6(ARSA):c.154G>A (p.Asp52Asn)
|
rs2146728012
|
|
NM_000487.6(ARSA):c.169G>A (p.Gly57Arg)
|
|
|
NM_000487.6(ARSA):c.173G>T (p.Gly58Val)
|
rs2082698425
|
|
NM_000487.6(ARSA):c.176T>C (p.Leu59Pro)
|
|
|
NM_000487.6(ARSA):c.17C>T (p.Pro6Leu)
|
|
|
NM_000487.6(ARSA):c.196G>A (p.Val66Met)
|
|
|
NM_000487.6(ARSA):c.200C>T (p.Pro67Leu)
|
rs765558965
|
|
NM_000487.6(ARSA):c.205T>C (p.Ser69Pro)
|
rs2146727641
|
|
NM_000487.6(ARSA):c.221C>G (p.Ser74Cys)
|
rs2146727534
|
|
NM_000487.6(ARSA):c.225-15T>C
|
|
|
NM_000487.6(ARSA):c.225-3C>G
|
rs756812838
|
|
NM_000487.6(ARSA):c.231_232delinsTT (p.Leu78Phe)
|
rs1603445011
|
|
NM_000487.6(ARSA):c.247C>T (p.Leu83Phe)
|
rs1603445008
|
|
NM_000487.6(ARSA):c.25C>A (p.Leu9Ile)
|
|
|
NM_000487.6(ARSA):c.264C>T (p.Gly88=)
|
|
|
NM_000487.6(ARSA):c.278T>G (p.Val93Gly)
|
rs2146726476
|
|
NM_000487.6(ARSA):c.28C>G (p.Leu10Val)
|
rs911532602
|
|
NM_000487.6(ARSA):c.295C>T (p.Arg99Trp)
|
|
|
NM_000487.6(ARSA):c.296G>A (p.Arg99Gln)
|
rs759295985
|
|
NM_000487.6(ARSA):c.296G>C (p.Arg99Pro)
|
rs759295985
|
|
NM_000487.6(ARSA):c.296G>T (p.Arg99Leu)
|
rs759295985
|
|
NM_000487.6(ARSA):c.308C>G (p.Pro103Arg)
|
|
|
NM_000487.6(ARSA):c.323C>T (p.Thr108Ile)
|
|
|
NM_000487.6(ARSA):c.326T>C (p.Val109Ala)
|
|
|
NM_000487.6(ARSA):c.329C>T (p.Ala110Val)
|
rs1191014984
|
|
NM_000487.6(ARSA):c.347G>A (p.Arg116Gln)
|
rs754795152
|
|
NM_000487.6(ARSA):c.349G>A (p.Gly117Ser)
|
rs2146725948
|
|
NM_000487.6(ARSA):c.349G>C (p.Gly117Arg)
|
|
|
NM_000487.6(ARSA):c.355C>G (p.Leu119Val)
|
rs1569081347
|
|
NM_000487.6(ARSA):c.388G>A (p.Val130Met)
|
|
|
NM_000487.6(ARSA):c.38T>A (p.Leu13Gln)
|
|
|
NM_000487.6(ARSA):c.392G>A (p.Gly131Glu)
|
rs1336260427
|
|
NM_000487.6(ARSA):c.394C>T (p.Pro132Ser)
|
|
|
NM_000487.6(ARSA):c.419A>T (p.His140Leu)
|
rs2082687894
|
|
NM_000487.6(ARSA):c.424G>A (p.Gly142Ser)
|
rs2146725322
|
|
NM_000487.6(ARSA):c.446T>C (p.Ile149Thr)
|
|
|
NM_000487.6(ARSA):c.454T>A (p.Ser152Thr)
|
|
|
NM_000487.6(ARSA):c.455C>G (p.Ser152Cys)
|
|
|
NM_000487.6(ARSA):c.460G>C (p.Asp154His)
|
|
|
NM_000487.6(ARSA):c.465+3A>G
|
rs2082686619
|
|
NM_000487.6(ARSA):c.465+5G>A
|
rs752777806
|
|
NM_000487.6(ARSA):c.473G>C (p.Cys158Ser)
|
rs1226689808
|
|
NM_000487.6(ARSA):c.484A>G (p.Thr162Ala)
|
|
|
NM_000487.6(ARSA):c.485C>G (p.Thr162Ser)
|
|
|
NM_000487.6(ARSA):c.488G>A (p.Cys163Tyr)
|
rs1430695346
|
|
NM_000487.6(ARSA):c.498G>A (p.Pro166=)
|
|
|
NM_000487.6(ARSA):c.511G>T (p.Asp171Tyr)
|
rs74315466
|
|
NM_000487.6(ARSA):c.518G>A (p.Gly173Asp)
|
|
|
NM_000487.6(ARSA):c.535G>A (p.Val179Ile)
|
|
|
NM_000487.6(ARSA):c.558C>A (p.Asn186Lys)
|
|
|
NM_000487.6(ARSA):c.562T>G (p.Ser188Ala)
|
rs1428555439
|
|
NM_000487.6(ARSA):c.565G>A (p.Val189Met)
|
|
|
NM_000487.6(ARSA):c.568G>C (p.Glu190Gln)
|
|
|
NM_000487.6(ARSA):c.571G>A (p.Ala191Thr)
|
rs2146723680
|
|
NM_000487.6(ARSA):c.577C>T (p.Pro193Ser)
|
|
|
NM_000487.6(ARSA):c.619G>A (p.Ala207Thr)
|
|
|
NM_000487.6(ARSA):c.620C>T (p.Ala207Val)
|
rs759098239
|
|
NM_000487.6(ARSA):c.633G>A (p.Met211Ile)
|
rs773059458
|
|
NM_000487.6(ARSA):c.635C>G (p.Ala212Gly)
|
|
|
NM_000487.6(ARSA):c.646C>T (p.Arg216Cys)
|
|
|
NM_000487.6(ARSA):c.658C>A (p.Pro220Thr)
|
|
|
NM_000487.6(ARSA):c.698C>G (p.Pro233Arg)
|
|
|
NM_000487.6(ARSA):c.724G>A (p.Glu242Lys)
|
rs757891932
|
|
NM_000487.6(ARSA):c.725A>G (p.Glu242Gly)
|
rs1403824251
|
|
NM_000487.6(ARSA):c.761T>C (p.Met254Thr)
|
rs1200786946
|
|
NM_000487.6(ARSA):c.781G>A (p.Gly261Arg)
|
rs138850940
|
|
NM_000487.6(ARSA):c.782G>A (p.Gly261Glu)
|
|
|
NM_000487.6(ARSA):c.800T>C (p.Ile267Thr)
|
|
|
NM_000487.6(ARSA):c.802G>A (p.Gly268Arg)
|
rs1404723529
|
|
NM_000487.6(ARSA):c.818T>C (p.Leu273Pro)
|
|
|
NM_000487.6(ARSA):c.820G>A (p.Glu274Lys)
|
|
|
NM_000487.6(ARSA):c.823G>A (p.Glu275Lys)
|
|
|
NM_000487.6(ARSA):c.823G>C (p.Glu275Gln)
|
|
|
NM_000487.6(ARSA):c.854G>A (p.Gly285Glu)
|
|
|
NM_000487.6(ARSA):c.913G>A (p.Gly305Arg)
|
rs2146720596
|
|
NM_000487.6(ARSA):c.937C>G (p.Arg313Gly)
|
rs551472773
|
|
NM_000487.6(ARSA):c.942G>T (p.Glu314Asp)
|
rs199476390
|
|
NM_000487.6(ARSA):c.953C>T (p.Ala318Val)
|
rs997702399
|
|
NM_000487.6(ARSA):c.967C>T (p.His323Tyr)
|
rs920501988
|
|
NM_000487.6(ARSA):c.973G>A (p.Ala325Thr)
|
|
|
NM_000487.6(ARSA):c.978C>T (p.Pro326=)
|
|
|
NM_000487.6(ARSA):c.980-21_980-20delinsCT
|
|
|
NM_000487.6(ARSA):c.981C>T (p.Gly327=)
|
|
|
NM_000487.6(ARSA):c.986C>G (p.Thr329Ser)
|
|
|