Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38605980_38605987delCA2580069739SCN5Ac.1305_1312del (p.Gln435HisfsTer22)
c.1176_1183del (p.Gln392HisfsTer22)
ClinVar
3g.38605979G>ACA057504SCN5Ac.1310C>T (p.Ala437Val)
c.1181C>T (p.Ala394Val)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38605979G>CCA352148407SCN5Ac.1310C>G (p.Ala437Gly)
c.1181C>G (p.Ala394Gly)
3g.38605979G=CA1358585923SCN5Ac.1310C= (p.Ala437=)
c.1181C= (p.Ala394=)
3g.38605979G>TCA352148405SCN5Ac.1310C>A (p.Ala437Asp)
c.1181C>A (p.Ala394Asp)
3g.38605980C>ACA352148413SCN5Ac.1309G>T (p.Ala437Ser)
c.1180G>T (p.Ala394Ser)
3g.38605980C=CA1358585924SCN5Ac.1309G= (p.Ala437=)
c.1180G= (p.Ala394=)
3g.38605980C>GCA352148410SCN5Ac.1309G>C (p.Ala437Pro)
c.1180G>C (p.Ala394Pro)
3g.38605980C>TCA352148412SCN5Ac.1309G>A (p.Ala437Thr)
c.1180G>A (p.Ala394Thr)
dbSNP gnomAD v3 gnomAD v4
3g.38605981C>ACA352148415SCN5Ac.1308G>T (p.Glu436Asp)
c.1179G>T (p.Glu393Asp)
3g.38605981C=CA1358585925SCN5Ac.1308G= (p.Glu436=)
c.1179G= (p.Glu393=)
3g.38605981C>GCA352148416SCN5Ac.1308G>C (p.Glu436Asp)
c.1179G>C (p.Glu393Asp)
3g.38605981C>TCA057493SCN5Ac.1308G>A (p.Glu436=)
c.1179G>A (p.Glu393=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38605982T>ACA352148419SCN5Ac.1307A>T (p.Glu436Val)
c.1178A>T (p.Glu393Val)
3g.38605982T>CCA352148421SCN5Ac.1307A>G (p.Glu436Gly)
c.1178A>G (p.Glu393Gly)
3g.38605982T>GCA352148423SCN5Ac.1307A>C (p.Glu436Ala)
c.1178A>C (p.Glu393Ala)
3g.38605983C>ACA352148425SCN5Ac.1306G>T (p.Glu436Ter)
c.1177G>T (p.Glu393Ter)
dbSNP
3g.38605983C=CA1358585926SCN5Ac.1306G= (p.Glu436=)
c.1177G= (p.Glu393=)
3g.38605983C>GCA352148426SCN5Ac.1306G>C (p.Glu436Gln)
c.1177G>C (p.Glu393Gln)
3g.38605983C>TCA352148428SCN5Ac.1306G>A (p.Glu436Lys)
c.1177G>A (p.Glu393Lys)
ClinVar dbSNP gnomAD v4
3g.38605984C>ACA352148430SCN5Ac.1305G>T (p.Gln435His)
c.1176G>T (p.Gln392His)
3g.38605984C>GCA352148431SCN5Ac.1305G>C (p.Gln435His)
c.1176G>C (p.Gln392His)
3g.38605984C>TCA433137535SCN5Ac.1305G>A (p.Gln435=)
c.1176G>A (p.Gln392=)
3g.38605985T>ACA352148436SCN5Ac.1304A>T (p.Gln435Leu)
c.1175A>T (p.Gln392Leu)
3g.38605985T>CCA352148434SCN5Ac.1304A>G (p.Gln435Arg)
c.1175A>G (p.Gln392Arg)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38605985T>GCA352148432SCN5Ac.1304A>C (p.Gln435Pro)
c.1175A>C (p.Gln392Pro)
3g.38605985T=CA1358585927SCN5Ac.1304A= (p.Gln435=)
c.1175A= (p.Gln392=)
3g.38605986G>ACA72940317SCN5Ac.1303C>T (p.Gln435Ter)
c.1174C>T (p.Gln392Ter)
dbSNP gnomAD v4
3g.38605986G>CCA352148439SCN5Ac.1303C>G (p.Gln435Glu)
c.1174C>G (p.Gln392Glu)
3g.38605986G=CA1358585928SCN5Ac.1303C= (p.Gln435=)
c.1174C= (p.Gln392=)
3g.38605986G>TCA352148441SCN5Ac.1303C>A (p.Gln435Lys)
c.1174C>A (p.Gln392Lys)
3g.38605987G>ACA014675SCN5Ac.1302C>T (p.Phe434=)
c.1173C>T (p.Phe391=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38605987G>CCA352148443SCN5Ac.1302C>G (p.Phe434Leu)
c.1173C>G (p.Phe391Leu)
3g.38605987G=CA1358585929SCN5Ac.1302C= (p.Phe434=)
c.1173C= (p.Phe391=)
3g.38605987G>TCA352148445SCN5Ac.1302C>A (p.Phe434Leu)
c.1173C>A (p.Phe391Leu)
3g.38605988A>CCA352148446SCN5Ac.1301T>G (p.Phe434Cys)
c.1172T>G (p.Phe391Cys)
3g.38605988A>GCA352148448SCN5Ac.1301T>C (p.Phe434Ser)
c.1172T>C (p.Phe391Ser)
3g.38605988A>TCA352148449SCN5Ac.1301T>A (p.Phe434Tyr)
c.1172T>A (p.Phe391Tyr)
3g.38605989A=CA1358585930SCN5Ac.1300T= (p.Phe434=)
c.1171T= (p.Phe391=)
3g.38605989A>CCA352148451SCN5Ac.1300T>G (p.Phe434Val)
c.1171T>G (p.Phe391Val)
dbSNP gnomAD v3 gnomAD v4
3g.38605989A>GCA352148453SCN5Ac.1300T>C (p.Phe434Leu)
c.1171T>C (p.Phe391Leu)
3g.38605989A>TCA352148455SCN5Ac.1300T>A (p.Phe434Ile)
c.1171T>A (p.Phe391Ile)
ClinVar
3g.38605990G>ACA057477SCN5Ac.1299C>T (p.Arg433=)
c.1170C>T (p.Arg390=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38605990G>CCA433137538SCN5Ac.1299C>G (p.Arg433=)
c.1170C>G (p.Arg390=)
3g.38605990G=CA1358585931SCN5Ac.1299C= (p.Arg433=)
c.1170C= (p.Arg390=)
3g.38605990G>TCA433137539SCN5Ac.1299C>A (p.Arg433=)
c.1170C>A (p.Arg390=)
3g.38605991C>ACA352148459SCN5Ac.1298G>T (p.Arg433Leu)
c.1169G>T (p.Arg390Leu)
gnomAD v4
3g.38605991C=CA1358585932SCN5Ac.1298G= (p.Arg433=)
c.1169G= (p.Arg390=)
3g.38605991C>GCA352148460SCN5Ac.1298G>C (p.Arg433Pro)
c.1169G>C (p.Arg390Pro)
3g.38605991C>TCA72940330SCN5Ac.1298G>A (p.Arg433His)
c.1169G>A (p.Arg390His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38605992G>ACA057469SCN5Ac.1297C>T (p.Arg433Cys)
c.1168C>T (p.Arg390Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38605992G>CCA352148463SCN5Ac.1297C>G (p.Arg433Gly)
c.1168C>G (p.Arg390Gly)
3g.38605992G=CA1358585933SCN5Ac.1297C= (p.Arg433=)
c.1168C= (p.Arg390=)
3g.38605992G>TCA057456SCN5Ac.1297C>A (p.Arg433Ser)
c.1168C>A (p.Arg390Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38605993C>ACA352148467SCN5Ac.1296G>T (p.Lys432Asn)
c.1167G>T (p.Lys389Asn)
3g.38605993C=CA1358585934SCN5Ac.1296G= (p.Lys432=)
c.1167G= (p.Lys389=)
3g.38605993C>GCA352148469SCN5Ac.1296G>C (p.Lys432Asn)
c.1167G>C (p.Lys389Asn)
3g.38605993C>TCA433137540SCN5Ac.1296G>A (p.Lys432=)
c.1167G>A (p.Lys389=)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38605994T>ACA352148471SCN5Ac.1295A>T (p.Lys432Met)
c.1166A>T (p.Lys389Met)
3g.38605994T>CCA352148472SCN5Ac.1295A>G (p.Lys432Arg)
c.1166A>G (p.Lys389Arg)
dbSNP
3g.38605994T>GCA352148473SCN5Ac.1295A>C (p.Lys432Thr)
c.1166A>C (p.Lys389Thr)
3g.38605995T>ACA352148477SCN5Ac.1294A>T (p.Lys432Ter)
c.1165A>T (p.Lys389Ter)
dbSNP
3g.38605995T>CCA352148478SCN5Ac.1294A>G (p.Lys432Glu)
c.1165A>G (p.Lys389Glu)
3g.38605995T>GCA352148480SCN5Ac.1294A>C (p.Lys432Gln)
c.1165A>C (p.Lys389Gln)
3g.38605995T=CA1358585935SCN5Ac.1294A= (p.Lys432=)
c.1165A= (p.Lys389=)
3g.38605996T>ACA352148483SCN5Ac.1293A>T (p.Glu431Asp)
c.1164A>T (p.Glu388Asp)
3g.38605996T>CCA433137545SCN5Ac.1293A>G (p.Glu431=)
c.1164A>G (p.Glu388=)
3g.38605996T>GCA352148484SCN5Ac.1293A>C (p.Glu431Asp)
c.1164A>C (p.Glu388Asp)
3g.38605997T>ACA352148488SCN5Ac.1292A>T (p.Glu431Val)
c.1163A>T (p.Glu388Val)
3g.38605997T>CCA352148492SCN5Ac.1292A>G (p.Glu431Gly)
c.1163A>G (p.Glu388Gly)
3g.38605997T>GCA352148490SCN5Ac.1292A>C (p.Glu431Ala)
c.1163A>C (p.Glu388Ala)
3g.38605998C>ACA352148493SCN5Ac.1291G>T (p.Glu431Ter)
c.1162G>T (p.Glu388Ter)
dbSNP
3g.38605998C=CA1358585936SCN5Ac.1291G= (p.Glu431=)
c.1162G= (p.Glu388=)
3g.38605998C>GCA352148495SCN5Ac.1291G>C (p.Glu431Gln)
c.1162G>C (p.Glu388Gln)
3g.38605998C>TCA352148498SCN5Ac.1291G>A (p.Glu431Lys)
c.1162G>A (p.Glu388Lys)
3g.38605999C>ACA352148501SCN5Ac.1290G>T (p.Lys430Asn)
c.1161G>T (p.Lys387Asn)
3g.38605999C>GCA352148502SCN5Ac.1290G>C (p.Lys430Asn)
c.1161G>C (p.Lys387Asn)
3g.38605999C>TCA433137547SCN5Ac.1290G>A (p.Lys430=)
c.1161G>A (p.Lys387=)
3g.38606000T>ACA352148504SCN5Ac.1289A>T (p.Lys430Met)
c.1160A>T (p.Lys387Met)
3g.38606000T>CCA352148506SCN5Ac.1289A>G (p.Lys430Arg)
c.1160A>G (p.Lys387Arg)
3g.38606000T>GCA352148508SCN5Ac.1289A>C (p.Lys430Thr)
c.1160A>C (p.Lys387Thr)
3g.38606001T>ACA352148510SCN5Ac.1288A>T (p.Lys430Ter)
c.1159A>T (p.Lys387Ter)
dbSNP
3g.38606001T>CCA352148512SCN5Ac.1288A>G (p.Lys430Glu)
c.1159A>G (p.Lys387Glu)
3g.38606001T>GCA352148514SCN5Ac.1288A>C (p.Lys430Gln)
c.1159A>C (p.Lys387Gln)
3g.38606001T=CA1358585938SCN5Ac.1288A= (p.Lys430=)
c.1159A= (p.Lys387=)
3g.38606001_38606004delinsTCTCCA1358585937SCN5Ac.1285_1288delinsGAGA (p.Glu429=)
c.1156_1159delinsGAGA (p.Glu386=)
3g.38606002C>ACA352148519SCN5Ac.1287G>T (p.Glu429Asp)
c.1158G>T (p.Glu386Asp)
ClinVar dbSNP
3g.38606002C=CA1358585939SCN5Ac.1287G= (p.Glu429=)
c.1158G= (p.Glu386=)
3g.38606002C>GCA352148521SCN5Ac.1287G>C (p.Glu429Asp)
c.1158G>C (p.Glu386Asp)
3g.38606002C>TCA057438SCN5Ac.1287G>A (p.Glu429=)
c.1158G>A (p.Glu386=)
ClinVar dbSNP ExAC gnomAD v2
3g.38606005_38606007delCA057434SCN5Ac.1285_1287del (p.Glu429del)
c.1156_1158del (p.Glu386del)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38606003T>ACA352148525SCN5Ac.1286A>T (p.Glu429Val)
c.1157A>T (p.Glu386Val)
3g.38606003T>CCA352148523SCN5Ac.1286A>G (p.Glu429Gly)
c.1157A>G (p.Glu386Gly)
ClinVar dbSNP
3g.38606003T>GCA352148526SCN5Ac.1286A>C (p.Glu429Ala)
c.1157A>C (p.Glu386Ala)
3g.38606004C>ACA352148528SCN5Ac.1285G>T (p.Glu429Ter)
c.1156G>T (p.Glu386Ter)
dbSNP
3g.38606004C=CA1358585940SCN5Ac.1285G= (p.Glu429=)
c.1156G= (p.Glu386=)
3g.38606004C>GCA352148530SCN5Ac.1285G>C (p.Glu429Gln)
c.1156G>C (p.Glu386Gln)
ClinVar dbSNP
3g.38606004C>TCA352148532SCN5Ac.1285G>A (p.Glu429Lys)
c.1156G>A (p.Glu386Lys)
dbSNP gnomAD v2 gnomAD v4
3g.38606005C>ACA352148534SCN5Ac.1284G>T (p.Glu428Asp)
c.1155G>T (p.Glu385Asp)
3g.38606005C>GCA352148536SCN5Ac.1284G>C (p.Glu428Asp)
c.1155G>C (p.Glu385Asp)
3g.38606005C>TCA433137550SCN5Ac.1284G>A (p.Glu428=)
c.1155G>A (p.Glu385=)
dbSNP COSMIC COSMIC COSMIC
3g.38606006T>ACA352148538SCN5Ac.1283A>T (p.Glu428Val)
c.1154A>T (p.Glu385Val)
3g.38606006T>CCA352148540SCN5Ac.1283A>G (p.Glu428Gly)
c.1154A>G (p.Glu385Gly)
3g.38606006T>GCA352148541SCN5Ac.1283A>C (p.Glu428Ala)
c.1154A>C (p.Glu385Ala)
3g.38606007C>ACA352148542SCN5Ac.1282G>T (p.Glu428Ter)
c.1153G>T (p.Glu385Ter)
dbSNP
3g.38606007C=CA1358585941SCN5Ac.1282G= (p.Glu428=)
c.1153G= (p.Glu385=)
3g.38606007C>GCA352148543SCN5Ac.1282G>C (p.Glu428Gln)
c.1153G>C (p.Glu385Gln)
gnomAD v4
3g.38606007C>TCA014651SCN5Ac.1282G>A (p.Glu428Lys)
c.1153G>A (p.Glu385Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38606008G>ACA014633SCN5Ac.1281C>T (p.Thr427=)
c.1152C>T (p.Thr384=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38606008G>CCA433137553SCN5Ac.1281C>G (p.Thr427=)
c.1152C>G (p.Thr384=)
3g.38606008G=CA1358585942SCN5Ac.1281C= (p.Thr427=)
c.1152C= (p.Thr384=)
3g.38606008G>TCA433137554SCN5Ac.1281C>A (p.Thr427=)
c.1152C>A (p.Thr384=)
3g.38606009G>ACA352148548SCN5Ac.1280C>T (p.Thr427Ile)
c.1151C>T (p.Thr384Ile)
3g.38606009G>CCA352148544SCN5Ac.1280C>G (p.Thr427Ser)
c.1151C>G (p.Thr384Ser)
3g.38606009G=CA1358585943SCN5Ac.1280C= (p.Thr427=)
c.1151C= (p.Thr384=)
3g.38606009G>TCA352148545SCN5Ac.1280C>A (p.Thr427Asn)
c.1151C>A (p.Thr384Asn)
ClinVar dbSNP
3g.38606010T>ACA352148550SCN5Ac.1279A>T (p.Thr427Ser)
c.1150A>T (p.Thr384Ser)
3g.38606010T>CCA352148551SCN5Ac.1279A>G (p.Thr427Ala)
c.1150A>G (p.Thr384Ala)
3g.38606010T>GCA352148553SCN5Ac.1279A>C (p.Thr427Pro)
c.1150A>C (p.Thr384Pro)
3g.38606011C>ACA352148554SCN5Ac.1278G>T (p.Glu426Asp)
c.1149G>T (p.Glu383Asp)
3g.38606011C>GCA352148557SCN5Ac.1278G>C (p.Glu426Asp)
c.1149G>C (p.Glu383Asp)
3g.38606011C>TCA433137557SCN5Ac.1278G>A (p.Glu426=)
c.1149G>A (p.Glu383=)
3g.38606012T>ACA352148560SCN5Ac.1277A>T (p.Glu426Val)
c.1148A>T (p.Glu383Val)
3g.38606012T>CCA352148561SCN5Ac.1277A>G (p.Glu426Gly)
c.1148A>G (p.Glu383Gly)
3g.38606012T>GCA352148563SCN5Ac.1277A>C (p.Glu426Ala)
c.1148A>C (p.Glu383Ala)
3g.38606013C>ACA352148565SCN5Ac.1276G>T (p.Glu426Ter)
c.1147G>T (p.Glu383Ter)
dbSNP
3g.38606013C=CA1358585944SCN5Ac.1276G= (p.Glu426=)
c.1147G= (p.Glu383=)
3g.38606013C>GCA352148567SCN5Ac.1276G>C (p.Glu426Gln)
c.1147G>C (p.Glu383Gln)
3g.38606013C>TCA352148569SCN5Ac.1276G>A (p.Glu426Lys)
c.1147G>A (p.Glu383Lys)
3g.38606014A>CCA433137558SCN5Ac.1275T>G (p.Ala425=)
c.1146T>G (p.Ala382=)
3g.38606014A>GCA433137559SCN5Ac.1275T>C (p.Ala425=)
c.1146T>C (p.Ala382=)
3g.38606014A>TCA433137560SCN5Ac.1275T>A (p.Ala425=)
c.1146T>A (p.Ala382=)
3g.38606015G>ACA352148573SCN5Ac.1274C>T (p.Ala425Val)
c.1145C>T (p.Ala382Val)
3g.38606015G>CCA352148571SCN5Ac.1274C>G (p.Ala425Gly)
c.1145C>G (p.Ala382Gly)
3g.38606015G>TCA352148570SCN5Ac.1274C>A (p.Ala425Asp)
c.1145C>A (p.Ala382Asp)
3g.38606016C>ACA352148576SCN5Ac.1273G>T (p.Ala425Ser)
c.1144G>T (p.Ala382Ser)
3g.38606016C=CA1358585945SCN5Ac.1273G= (p.Ala425=)
c.1144G= (p.Ala382=)
3g.38606016C>GCA057417SCN5Ac.1273G>C (p.Ala425Pro)
c.1144G>C (p.Ala382Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38606016C>TCA014623SCN5Ac.1273G>A (p.Ala425Thr)
c.1144G>A (p.Ala382Thr)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38606017G>ACA057412SCN5Ac.1272C>T (p.Ile424=)
c.1143C>T (p.Ile381=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38606017G>CCA057406SCN5Ac.1272C>G (p.Ile424Met)
c.1143C>G (p.Ile381Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38606017G=CA1358585946SCN5Ac.1272C= (p.Ile424=)
c.1143C= (p.Ile381=)
3g.38606017G>TCA433137562SCN5Ac.1272C>A (p.Ile424=)
c.1143C>A (p.Ile381=)
3g.38606018A>CCA352148588SCN5Ac.1271T>G (p.Ile424Ser)
c.1142T>G (p.Ile381Ser)
3g.38606018A>GCA352148586SCN5Ac.1271T>C (p.Ile424Thr)
c.1142T>C (p.Ile381Thr)
3g.38606018A>TCA352148584SCN5Ac.1271T>A (p.Ile424Asn)
c.1142T>A (p.Ile381Asn)
3g.38606019T>ACA352148590SCN5Ac.1270A>T (p.Ile424Phe)
c.1141A>T (p.Ile381Phe)
3g.38606019T>CCA352148592SCN5Ac.1270A>G (p.Ile424Val)
c.1141A>G (p.Ile381Val)
gnomAD v4
3g.38606019T>GCA352148594SCN5Ac.1270A>C (p.Ile424Leu)
c.1141A>C (p.Ile381Leu)
3g.38606020G>ACA433137563SCN5Ac.1269C>T (p.Thr423=)
c.1140C>T (p.Thr380=)
ClinVar dbSNP gnomAD v4
3g.38606020G>CCA433137564SCN5Ac.1269C>G (p.Thr423=)
c.1140C>G (p.Thr380=)
3g.38606020G>TCA433137565SCN5Ac.1269C>A (p.Thr423=)
c.1140C>A (p.Thr380=)
3g.38606021G>ACA352148597SCN5Ac.1268C>T (p.Thr423Ile)
c.1139C>T (p.Thr380Ile)
dbSNP gnomAD v4
3g.38606021G>CCA352148598SCN5Ac.1268C>G (p.Thr423Ser)
c.1139C>G (p.Thr380Ser)
3g.38606021G=CA1358585947SCN5Ac.1268C= (p.Thr423=)
c.1139C= (p.Thr380=)
3g.38606021G>TCA352148599SCN5Ac.1268C>A (p.Thr423Asn)
c.1139C>A (p.Thr380Asn)
3g.38606022T>ACA352148601SCN5Ac.1267A>T (p.Thr423Ser)
c.1138A>T (p.Thr380Ser)
3g.38606022T>CCA352148605SCN5Ac.1267A>G (p.Thr423Ala)
c.1138A>G (p.Thr380Ala)
gnomAD v4
3g.38606022T>GCA352148603SCN5Ac.1267A>C (p.Thr423Pro)
c.1138A>C (p.Thr380Pro)
dbSNP
3g.38606022T=CA1358585948SCN5Ac.1267A= (p.Thr423=)
c.1138A= (p.Thr380=)
3g.38606023G>ACA433137566SCN5Ac.1266C>T (p.Ala422=)
c.1137C>T (p.Ala379=)
ClinVar dbSNP
3g.38606023G>CCA433137567SCN5Ac.1266C>G (p.Ala422=)
c.1137C>G (p.Ala379=)
3g.38606023G>TCA433137568SCN5Ac.1266C>A (p.Ala422=)
c.1137C>A (p.Ala379=)
3g.38606024G>ACA352148607SCN5Ac.1265C>T (p.Ala422Val)
c.1136C>T (p.Ala379Val)
3g.38606024G>CCA352148608SCN5Ac.1265C>G (p.Ala422Gly)
c.1136C>G (p.Ala379Gly)
gnomAD v4
3g.38606024G>TCA352148610SCN5Ac.1265C>A (p.Ala422Asp)
c.1136C>A (p.Ala379Asp)
3g.38606025C>ACA352148611SCN5Ac.1264G>T (p.Ala422Ser)
c.1135G>T (p.Ala379Ser)
3g.38606025C>GCA352148613SCN5Ac.1264G>C (p.Ala422Pro)
c.1135G>C (p.Ala379Pro)
3g.38606025C>TCA352148615SCN5Ac.1264G>A (p.Ala422Thr)
c.1135G>A (p.Ala379Thr)
ClinVar dbSNP
3g.38606026T>ACA352148617SCN5Ac.1263A>T (p.Gln421His)
c.1134A>T (p.Gln378His)
3g.38606026T>CCA433137569SCN5Ac.1263A>G (p.Gln421=)
c.1134A>G (p.Gln378=)
3g.38606026T>GCA352148619SCN5Ac.1263A>C (p.Gln421His)
c.1134A>C (p.Gln378His)
3g.38606027T>ACA352148621SCN5Ac.1262A>T (p.Gln421Leu)
c.1133A>T (p.Gln378Leu)
3g.38606027T>CCA352148623SCN5Ac.1262A>G (p.Gln421Arg)
c.1133A>G (p.Gln378Arg)
3g.38606027T>GCA352148625SCN5Ac.1262A>C (p.Gln421Pro)
c.1133A>C (p.Gln378Pro)
ClinVar dbSNP
3g.38606027T=CA1358585949SCN5Ac.1262A= (p.Gln421=)
c.1133A= (p.Gln378=)
3g.38606028G>ACA72940336SCN5Ac.1261C>T (p.Gln421Ter)
c.1132C>T (p.Gln378Ter)
dbSNP
3g.38606028G>CCA352148628SCN5Ac.1261C>G (p.Gln421Glu)
c.1132C>G (p.Gln378Glu)
3g.38606028G=CA1358585950SCN5Ac.1261C= (p.Gln421=)
c.1132C= (p.Gln378=)
3g.38606028G>TCA352148627SCN5Ac.1261C>A (p.Gln421Lys)
c.1132C>A (p.Gln378Lys)
3g.38606029G>ACA433137570SCN5Ac.1260C>T (p.Asn420=)
c.1131C>T (p.Asn377=)
3g.38606029G>CCA352148632SCN5Ac.1260C>G (p.Asn420Lys)
c.1131C>G (p.Asn377Lys)
3g.38606029G>TCA352148631SCN5Ac.1260C>A (p.Asn420Lys)
c.1131C>A (p.Asn377Lys)
3g.38606030T>ACA352148634SCN5Ac.1259A>T (p.Asn420Ile)
c.1130A>T (p.Asn377Ile)
3g.38606030T>CCA352148635SCN5Ac.1259A>G (p.Asn420Ser)
c.1130A>G (p.Asn377Ser)
3g.38606030T>GCA352148636SCN5Ac.1259A>C (p.Asn420Thr)
c.1130A>C (p.Asn377Thr)
3g.38606031T>ACA352148637SCN5Ac.1258A>T (p.Asn420Tyr)
c.1129A>T (p.Asn377Tyr)
3g.38606031T>CCA352148638SCN5Ac.1258A>G (p.Asn420Asp)
c.1129A>G (p.Asn377Asp)
3g.38606031T>GCA352148640SCN5Ac.1258A>C (p.Asn420His)
c.1129A>C (p.Asn377His)
3g.38606032T>ACA352148643SCN5Ac.1257A>T (p.Gln419His)
c.1128A>T (p.Gln376His)
3g.38606032T>CCA433137571SCN5Ac.1257A>G (p.Gln419=)
c.1128A>G (p.Gln376=)
3g.38606032T>GCA352148645SCN5Ac.1257A>C (p.Gln419His)
c.1128A>C (p.Gln376His)
3g.38606033T>ACA352148647SCN5Ac.1256A>T (p.Gln419Leu)
c.1127A>T (p.Gln376Leu)
3g.38606033T>CCA352148648SCN5Ac.1256A>G (p.Gln419Arg)
c.1127A>G (p.Gln376Arg)
3g.38606033T>GCA16604921SCN5Ac.1256A>C (p.Gln419Pro)
c.1127A>C (p.Gln376Pro)
ClinVar dbSNP
3g.38606033T=CA1358585951SCN5Ac.1256A= (p.Gln419=)
c.1127A= (p.Gln376=)
3g.38606034G>ACA16043398SCN5Ac.1255C>T (p.Gln419Ter)
c.1126C>T (p.Gln376Ter)
ClinVar dbSNP
3g.38606034G>CCA352148654SCN5Ac.1255C>G (p.Gln419Glu)
c.1126C>G (p.Gln376Glu)
ClinVar dbSNP
3g.38606034G=CA1358585952SCN5Ac.1255C= (p.Gln419=)
c.1126C= (p.Gln376=)
3g.38606034G>TCA352148651SCN5Ac.1255C>A (p.Gln419Lys)
c.1126C>A (p.Gln376Lys)
3g.38606035C>ACA352148656SCN5Ac.1254G>T (p.Glu418Asp)
c.1125G>T (p.Glu375Asp)
3g.38606035C>GCA352148658SCN5Ac.1254G>C (p.Glu418Asp)
c.1125G>C (p.Glu375Asp)
3g.38606035C>TCA433137572SCN5Ac.1254G>A (p.Glu418=)
c.1125G>A (p.Glu375=)
gnomAD v4
3g.38606036T>ACA352148660SCN5Ac.1253A>T (p.Glu418Val)
c.1124A>T (p.Glu375Val)
3g.38606036T>CCA352148661SCN5Ac.1253A>G (p.Glu418Gly)
c.1124A>G (p.Glu375Gly)
ClinVar
3g.38606036T>GCA352148664SCN5Ac.1253A>C (p.Glu418Ala)
c.1124A>C (p.Glu375Ala)
3g.38606037C>ACA352012SCN5Ac.1252G>T (p.Glu418Ter)
c.1123G>T (p.Glu375Ter)
ClinVar dbSNP
3g.38606037C=CA1358585953SCN5Ac.1252G= (p.Glu418=)
c.1123G= (p.Glu375=)
3g.38606037C>GCA352148666SCN5Ac.1252G>C (p.Glu418Gln)
c.1123G>C (p.Glu375Gln)
3g.38606037C>TCA352148668SCN5Ac.1252G>A (p.Glu418Lys)
c.1123G>A (p.Glu375Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38606038C>ACA352148671SCN5Ac.1251G>T (p.Glu417Asp)
c.1122G>T (p.Glu374Asp)
3g.38606038C>GCA352148673SCN5Ac.1251G>C (p.Glu417Asp)
c.1122G>C (p.Glu374Asp)
3g.38606038C>TCA433137573SCN5Ac.1251G>A (p.Glu417=)
c.1122G>A (p.Glu374=)
ClinVar COSMIC COSMIC COSMIC
3g.38606039T>ACA352148674SCN5Ac.1250A>T (p.Glu417Val)
c.1121A>T (p.Glu374Val)
3g.38606039T>CCA352148676SCN5Ac.1250A>G (p.Glu417Gly)
c.1121A>G (p.Glu374Gly)
3g.38606039T>GCA352148678SCN5Ac.1250A>C (p.Glu417Ala)
c.1121A>C (p.Glu374Ala)
3g.38606040C>ACA352148684SCN5Ac.1249G>T (p.Glu417Ter)
c.1120G>T (p.Glu374Ter)
dbSNP
3g.38606040C=CA1358585954SCN5Ac.1249G= (p.Glu417=)
c.1120G= (p.Glu374=)
3g.38606040C>GCA352148683SCN5Ac.1249G>C (p.Glu417Gln)
c.1120G>C (p.Glu374Gln)
3g.38606040C>TCA352148680SCN5Ac.1249G>A (p.Glu417Lys)
c.1120G>A (p.Glu374Lys)
3g.38606041A>CCA352148686SCN5Ac.1248T>G (p.Tyr416Ter)
c.1119T>G (p.Tyr373Ter)
3g.38606041A>GCA433137574SCN5Ac.1248T>C (p.Tyr416=)
c.1119T>C (p.Tyr373=)
3g.38606041A>TCA352148687SCN5Ac.1248T>A (p.Tyr416Ter)
c.1119T>A (p.Tyr373Ter)
3g.38606042T>ACA352148688SCN5Ac.1247A>T (p.Tyr416Phe)
c.1118A>T (p.Tyr373Phe)
3g.38606042T>CCA014608SCN5Ac.1247A>G (p.Tyr416Cys)
c.1118A>G (p.Tyr373Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38606042T>GCA352148690SCN5Ac.1247A>C (p.Tyr416Ser)
c.1118A>C (p.Tyr373Ser)
3g.38606042T=CA1358585955SCN5Ac.1247A= (p.Tyr416=)
c.1118A= (p.Tyr373=)
3g.38606043delCA2580069740SCN5Ac.1246del (p.Tyr416MetfsTer?)
c.1117del (p.Tyr373MetfsTer?)
ClinVar
3g.38606043A>CCA352148692SCN5Ac.1246T>G (p.Tyr416Asp)
c.1117T>G (p.Tyr373Asp)
3g.38606043A>GCA352148694SCN5Ac.1246T>C (p.Tyr416His)
c.1117T>C (p.Tyr373His)
3g.38606043A>TCA352148696SCN5Ac.1246T>A (p.Tyr416Asn)
c.1117T>A (p.Tyr373Asn)
3g.38606044G>ACA433137577SCN5Ac.1245C>T (p.Ala415=)
c.1116C>T (p.Ala372=)
ClinVar dbSNP
3g.38606044G>CCA433137575SCN5Ac.1245C>G (p.Ala415=)
c.1116C>G (p.Ala372=)
3g.38606044G>TCA433137576SCN5Ac.1245C>A (p.Ala415=)
c.1116C>A (p.Ala372=)
3g.38606045G>ACA352148698SCN5Ac.1244C>T (p.Ala415Val)
c.1115C>T (p.Ala372Val)
3g.38606045G>CCA352148699SCN5Ac.1244C>G (p.Ala415Gly)
c.1115C>G (p.Ala372Gly)
3g.38606045G>TCA352148701SCN5Ac.1244C>A (p.Ala415Asp)
c.1115C>A (p.Ala372Asp)
3g.38606046C>ACA352148703SCN5Ac.1243G>T (p.Ala415Ser)
c.1114G>T (p.Ala372Ser)
gnomAD v4
3g.38606046C=CA1358585956SCN5Ac.1243G= (p.Ala415=)
c.1114G= (p.Ala372=)
3g.38606046C>GCA352148705SCN5Ac.1243G>C (p.Ala415Pro)
c.1114G>C (p.Ala372Pro)
ClinVar dbSNP
3g.38606046C>TCA057393SCN5Ac.1243G>A (p.Ala415Thr)
c.1114G>A (p.Ala372Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38606047C>ACA352148708SCN5Ac.1242G>T (p.Met414Ile)
c.1113G>T (p.Met371Ile)
ClinVar
3g.38606047C>GCA352148707SCN5Ac.1242G>C (p.Met414Ile)
c.1113G>C (p.Met371Ile)
3g.38606047C>TCA352148706SCN5Ac.1242G>A (p.Met414Ile)
c.1113G>A (p.Met371Ile)
3g.38606048A>CCA352148709SCN5Ac.1241T>G (p.Met414Arg)
c.1112T>G (p.Met371Arg)
3g.38606048A>GCA352148711SCN5Ac.1241T>C (p.Met414Thr)
c.1112T>C (p.Met371Thr)
3g.38606048A>TCA352148712SCN5Ac.1241T>A (p.Met414Lys)
c.1112T>A (p.Met371Lys)
3g.38606049T>ACA352148713SCN5Ac.1240A>T (p.Met414Leu)
c.1111A>T (p.Met371Leu)
3g.38606049T>CCA352148716SCN5Ac.1240A>G (p.Met414Val)
c.1111A>G (p.Met371Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38606049T>GCA352148717SCN5Ac.1240A>C (p.Met414Leu)
c.1111A>C (p.Met371Leu)
3g.38606049T=CA1358585957SCN5Ac.1240A= (p.Met414=)
c.1111A= (p.Met371=)
3g.38606050T>ACA433137580SCN5Ac.1239A>T (p.Ala413=)
c.1110A>T (p.Ala370=)
3g.38606050T>CCA433137579SCN5Ac.1239A>G (p.Ala413=)
c.1110A>G (p.Ala370=)
3g.38606050T>GCA433137578SCN5Ac.1239A>C (p.Ala413=)
c.1110A>C (p.Ala370=)
3g.38606051G>ACA352148719SCN5Ac.1238C>T (p.Ala413Val)
c.1109C>T (p.Ala370Val)
3g.38606051G>CCA352148720SCN5Ac.1238C>G (p.Ala413Gly)
c.1109C>G (p.Ala370Gly)
3g.38606051G=CA1358585958SCN5Ac.1238C= (p.Ala413=)
c.1109C= (p.Ala370=)
3g.38606051G>TCA014593SCN5Ac.1238C>A (p.Ala413Glu)
c.1109C>A (p.Ala370Glu)
ClinVar dbSNP
3g.38606052C>ACA10576617SCN5Ac.1237G>T (p.Ala413Ser)
c.1108G>T (p.Ala370Ser)
ClinVar dbSNP gnomAD v4
3g.38606052C=CA1358585959SCN5Ac.1237G= (p.Ala413=)
c.1108G= (p.Ala370=)
3g.38606052C>GCA352148724SCN5Ac.1237G>C (p.Ala413Pro)
c.1108G>C (p.Ala370Pro)
3g.38606052C>TCA014582SCN5Ac.1237G>A (p.Ala413Thr)
c.1108G>A (p.Ala370Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38606053G>ACA014570SCN5Ac.1236C>T (p.Val412=)
c.1107C>T (p.Val369=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38606053G>CCA433137581SCN5Ac.1236C>G (p.Val412=)
c.1107C>G (p.Val369=)
ClinVar
3g.38606053G=CA1358585960SCN5Ac.1236C= (p.Val412=)
c.1107C= (p.Val369=)
3g.38606053G>TCA433137582SCN5Ac.1236C>A (p.Val412=)
c.1107C>A (p.Val369=)
COSMIC
3g.38606054A>CCA352148729SCN5Ac.1235T>G (p.Val412Gly)
c.1106T>G (p.Val369Gly)
3g.38606054A>GCA352148730SCN5Ac.1235T>C (p.Val412Ala)
c.1106T>C (p.Val369Ala)
3g.38606054A>TCA352148728SCN5Ac.1235T>A (p.Val412Asp)
c.1106T>A (p.Val369Asp)
3g.38606055C>ACA352148734SCN5Ac.1234G>T (p.Val412Phe)
c.1105G>T (p.Val369Phe)
3g.38606055C>GCA352148732SCN5Ac.1234G>C (p.Val412Leu)
c.1105G>C (p.Val369Leu)
3g.38606055C>TCA352148735SCN5Ac.1234G>A (p.Val412Ile)
c.1105G>A (p.Val369Ile)
3g.38606056delCA2586971905SCN5Ac.1234del (p.Val412SerfsTer?)
c.1105del (p.Val369SerfsTer?)
ClinVar
3g.38606056C>ACA433137583SCN5Ac.1233G>T (p.Val411=)
c.1104G>T (p.Val368=)
ClinVar dbSNP
3g.38606056C=CA1358585961SCN5Ac.1233G= (p.Val411=)
c.1104G= (p.Val368=)
3g.38606056C>GCA433137584SCN5Ac.1233G>C (p.Val411=)
c.1104G>C (p.Val368=)
3g.38606056C>TCA433137585SCN5Ac.1233G>A (p.Val411=)
c.1104G>A (p.Val368=)
dbSNP gnomAD v2 gnomAD v4
3g.38606057A=CA1358585962SCN5Ac.1232T= (p.Val411=)
c.1103T= (p.Val368=)
3g.38606057A>CCA352148736SCN5Ac.1232T>G (p.Val411Gly)
c.1103T>G (p.Val368Gly)
3g.38606057A>GCA352148738SCN5Ac.1232T>C (p.Val411Ala)
c.1103T>C (p.Val368Ala)
dbSNP
3g.38606057A>TCA352148737SCN5Ac.1232T>A (p.Val411Glu)
c.1103T>A (p.Val368Glu)
3g.38606058C>ACA352148739SCN5Ac.1231G>T (p.Val411Leu)
c.1102G>T (p.Val368Leu)
3g.38606058C=CA1358585963SCN5Ac.1231G= (p.Val411=)
c.1102G= (p.Val368=)
3g.38606058C>GCA352148742SCN5Ac.1231G>C (p.Val411Leu)
c.1102G>C (p.Val368Leu)
3g.38606058C>TCA014560SCN5Ac.1231G>A (p.Val411Met)
c.1102G>A (p.Val368Met)
ClinVar dbSNP
3g.38606058_38606059delinsCGCA1358585964SCN5Ac.1230_1231delinsCG (p.Ala410=)
c.1101_1102delinsCG (p.Ala367=)
3g.38606059G>ACA057374SCN5Ac.1230C>T (p.Ala410=)
c.1101C>T (p.Ala367=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38606059G>CCA433137586SCN5Ac.1230C>G (p.Ala410=)
c.1101C>G (p.Ala367=)
3g.38606059G=CA1358585966SCN5Ac.1230C= (p.Ala410=)
c.1101C= (p.Ala367=)
3g.38606059G>TCA433137587SCN5Ac.1230C>A (p.Ala410=)
c.1101C>A (p.Ala367=)
ClinVar gnomAD v4
3g.38606060delCA1358585965SCN5Ac.1230del (p.Val411TrpfsTer?)
c.1101del (p.Val368TrpfsTer?)
ClinVar dbSNP
3g.38606060G>ACA057370SCN5Ac.1229C>T (p.Ala410Val)
c.1100C>T (p.Ala367Val)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38606060G>CCA352148747SCN5Ac.1229C>G (p.Ala410Gly)
c.1100C>G (p.Ala367Gly)
3g.38606060G=CA1358585967SCN5Ac.1229C= (p.Ala410=)
c.1100C= (p.Ala367=)
3g.38606060G>TCA352148752SCN5Ac.1229C>A (p.Ala410Asp)
c.1100C>A (p.Ala367Asp)
3g.38606061C>ACA352148754SCN5Ac.1228G>T (p.Ala410Ser)
c.1099G>T (p.Ala367Ser)
3g.38606061C>GCA352148757SCN5Ac.1228G>C (p.Ala410Pro)
c.1099G>C (p.Ala367Pro)
3g.38606061C>TCA352148759SCN5Ac.1228G>A (p.Ala410Thr)
c.1099G>A (p.Ala367Thr)
3g.38606062C>ACA433137588SCN5Ac.1227G>T (p.Leu409=)
c.1098G>T (p.Leu366=)
3g.38606062C=CA1358585968SCN5Ac.1227G= (p.Leu409=)
c.1098G= (p.Leu366=)
3g.38606062C>GCA433137589SCN5Ac.1227G>C (p.Leu409=)
c.1098G>C (p.Leu366=)
3g.38606062C>TCA433137590SCN5Ac.1227G>A (p.Leu409=)
c.1098G>A (p.Leu366=)
dbSNP gnomAD v3 gnomAD v4
3g.38606062_38606063insTATGCA1139655785SCN5Ac.1226_1227insCATA (p.Ala410IlefsTer9)
c.1097_1098insCATA (p.Ala367IlefsTer9)
ClinVar dbSNP
3g.38606063A>CCA352148761SCN5Ac.1226T>G (p.Leu409Arg)
c.1097T>G (p.Leu366Arg)
3g.38606063A>GCA352148763SCN5Ac.1226T>C (p.Leu409Pro)
c.1097T>C (p.Leu366Pro)
3g.38606063A>TCA352148764SCN5Ac.1226T>A (p.Leu409Gln)
c.1097T>A (p.Leu366Gln)
3g.38606063_38606064delCA2697550810SCN5Ac.1225_1226del (p.Leu409GlyfsTer8)
c.1096_1097del (p.Leu366GlyfsTer8)
ClinVar
3g.38606064G>ACA433137591SCN5Ac.1225C>T (p.Leu409=)
c.1096C>T (p.Leu366=)
COSMIC COSMIC COSMIC
3g.38606064G>CCA014550SCN5Ac.1225C>G (p.Leu409Val)
c.1096C>G (p.Leu366Val)
ClinVar dbSNP
3g.38606064G=CA1358585969SCN5Ac.1225C= (p.Leu409=)
c.1096C= (p.Leu366=)
3g.38606064G>TCA352148767SCN5Ac.1225C>A (p.Leu409Met)
c.1096C>A (p.Leu366Met)
3g.38606065G>ACA433137592SCN5Ac.1224C>T (p.Ile408=)
c.1095C>T (p.Ile365=)
gnomAD v4 COSMIC COSMIC COSMIC
3g.38606065G>CCA352148770SCN5Ac.1224C>G (p.Ile408Met)
c.1095C>G (p.Ile365Met)
3g.38606065G>TCA433137593SCN5Ac.1224C>A (p.Ile408=)
c.1095C>A (p.Ile365=)
ClinVar
3g.38606066A>CCA352148772SCN5Ac.1223T>G (p.Ile408Ser)
c.1094T>G (p.Ile365Ser)
3g.38606066A>GCA352148773SCN5Ac.1223T>C (p.Ile408Thr)
c.1094T>C (p.Ile365Thr)
3g.38606066A>TCA352148775SCN5Ac.1223T>A (p.Ile408Asn)
c.1094T>A (p.Ile365Asn)
3g.38606067T>ACA352148778SCN5Ac.1222A>T (p.Ile408Phe)
c.1093A>T (p.Ile365Phe)
3g.38606067T>CCA352148779SCN5Ac.1222A>G (p.Ile408Val)
c.1093A>G (p.Ile365Val)
3g.38606067T>GCA352148780SCN5Ac.1222A>C (p.Ile408Leu)
c.1093A>C (p.Ile365Leu)
3g.38606068C>ACA433137595SCN5Ac.1221G>T (p.Leu407=)
c.1092G>T (p.Leu364=)
ClinVar dbSNP
3g.38606068C=CA1358585970SCN5Ac.1221G= (p.Leu407=)
c.1092G= (p.Leu364=)
3g.38606068C>GCA433137596SCN5Ac.1221G>C (p.Leu407=)
c.1092G>C (p.Leu364=)
ClinVar
3g.38606068C>TCA433137594SCN5Ac.1221G>A (p.Leu407=)
c.1092G>A (p.Leu364=)
COSMIC COSMIC COSMIC
3g.38606069A>CCA352148781SCN5Ac.1220T>G (p.Leu407Arg)
c.1091T>G (p.Leu364Arg)
3g.38606069A>GCA352148783SCN5Ac.1220T>C (p.Leu407Pro)
c.1091T>C (p.Leu364Pro)
3g.38606069A>TCA352148785SCN5Ac.1220T>A (p.Leu407Gln)
c.1091T>A (p.Leu364Gln)
3g.38606070G>ACA433137597SCN5Ac.1219C>T (p.Leu407=)
c.1090C>T (p.Leu364=)
dbSNP gnomAD v3 gnomAD v4
3g.38606070G>CCA352148786SCN5Ac.1219C>G (p.Leu407Val)
c.1090C>G (p.Leu364Val)
3g.38606070G=CA1358585971SCN5Ac.1219C= (p.Leu407=)
c.1090C= (p.Leu364=)
3g.38606070G>TCA352148787SCN5Ac.1219C>A (p.Leu407Met)
c.1090C>A (p.Leu364Met)
3g.38606071G>ACA057362SCN5Ac.1218C>T (p.Asn406=)
c.1089C>T (p.Asn363=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38606071G>CCA014540SCN5Ac.1218C>G (p.Asn406Lys)
c.1089C>G (p.Asn363Lys)
ClinVar dbSNP
3g.38606071G=CA1358585972SCN5Ac.1218C= (p.Asn406=)
c.1089C= (p.Asn363=)
3g.38606071G>TCA014532SCN5Ac.1218C>A (p.Asn406Lys)
c.1089C>A (p.Asn363Lys)
ClinVar dbSNP
3g.38606072T>ACA352148790SCN5Ac.1217A>T (p.Asn406Ile)
c.1088A>T (p.Asn363Ile)
ClinVar
3g.38606072T>CCA014519SCN5Ac.1217A>G (p.Asn406Ser)
c.1088A>G (p.Asn363Ser)
ClinVar dbSNP
3g.38606072T>GCA352148793SCN5Ac.1217A>C (p.Asn406Thr)
c.1088A>C (p.Asn363Thr)
3g.38606072T=CA1358585973SCN5Ac.1217A= (p.Asn406=)
c.1088A= (p.Asn363=)
3g.38606073T>ACA352148795SCN5Ac.1216A>T (p.Asn406Tyr)
c.1087A>T (p.Asn363Tyr)
3g.38606073T>CCA352148797SCN5Ac.1216A>G (p.Asn406Asp)
c.1087A>G (p.Asn363Asp)
3g.38606073T>GCA352148798SCN5Ac.1216A>C (p.Asn406His)
c.1087A>C (p.Asn363His)
3g.38606074C>ACA433137600SCN5Ac.1215G>T (p.Val405=)
c.1086G>T (p.Val362=)
3g.38606074C>GCA433137599SCN5Ac.1215G>C (p.Val405=)
c.1086G>C (p.Val362=)
3g.38606074C>TCA433137598SCN5Ac.1215G>A (p.Val405=)
c.1086G>A (p.Val362=)
3g.38606075A>CCA352148800SCN5Ac.1214T>G (p.Val405Gly)
c.1085T>G (p.Val362Gly)
gnomAD v4
3g.38606075A>GCA352148801SCN5Ac.1214T>C (p.Val405Ala)
c.1085T>C (p.Val362Ala)
3g.38606075A>TCA352148803SCN5Ac.1214T>A (p.Val405Glu)
c.1085T>A (p.Val362Glu)
3g.38606076C>ACA352148805SCN5Ac.1213G>T (p.Val405Leu)
c.1084G>T (p.Val362Leu)
3g.38606076C=CA1358585974SCN5Ac.1213G= (p.Val405=)
c.1084G= (p.Val362=)
3g.38606076C>GCA352148807SCN5Ac.1213G>C (p.Val405Leu)
c.1084G>C (p.Val362Leu)
ClinVar dbSNP
3g.38606076C>TCA352148809SCN5Ac.1213G>A (p.Val405Met)
c.1084G>A (p.Val362Met)
3g.38606077C>ACA433137601SCN5Ac.1212G>T (p.Leu404=)
c.1083G>T (p.Leu361=)
ClinVar dbSNP
3g.38606077C=CA1358585975SCN5Ac.1212G= (p.Leu404=)
c.1083G= (p.Leu361=)
3g.38606077C>GCA433137602SCN5Ac.1212G>C (p.Leu404=)
c.1083G>C (p.Leu361=)
dbSNP
3g.38606077C>TCA433137603SCN5Ac.1212G>A (p.Leu404=)
c.1083G>A (p.Leu361=)
3g.38606078A=CA1358585976SCN5Ac.1211T= (p.Leu404=)
c.1082T= (p.Leu361=)
3g.38606078A>CCA352148814SCN5Ac.1211T>G (p.Leu404Arg)
c.1082T>G (p.Leu361Arg)
3g.38606078A>GCA352148811SCN5Ac.1211T>C (p.Leu404Pro)
c.1082T>C (p.Leu361Pro)
3g.38606078A>TCA014506SCN5Ac.1211T>A (p.Leu404Gln)
c.1082T>A (p.Leu361Gln)
ClinVar dbSNP
3g.38606079G>ACA433137604SCN5Ac.1210C>T (p.Leu404=)
c.1081C>T (p.Leu361=)
gnomAD v4
3g.38606079G>CCA057353SCN5Ac.1210C>G (p.Leu404Val)
c.1081C>G (p.Leu361Val)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38606079G=CA1358585977SCN5Ac.1210C= (p.Leu404=)
c.1081C= (p.Leu361=)
3g.38606079G>TCA352148817SCN5Ac.1210C>A (p.Leu404Met)
c.1081C>A (p.Leu361Met)

Number of alleles fetched