Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38566521_38566523delCA2580069777SCN5Ac.3724_3726del (p.Asp1242del)
c.3727_3729del (p.Asp1243del)
c.3565_3567del (p.Asp1189del)
c.3598_3600del (p.Asp1200del)
 ClinVar
3g.38566522C>ACA352149270SCN5Ac.3724G>T (p.Asp1242Tyr)
c.3727G>T (p.Asp1243Tyr)
c.3565G>T (p.Asp1189Tyr)
c.3598G>T (p.Asp1200Tyr)
 ClinVar
3g.38566522C=CA1358569704SCN5Ac.3724G= (p.Asp1242=)
c.3727G= (p.Asp1243=)
c.3565G= (p.Asp1189=)
c.3598G= (p.Asp1200=)
3g.38566522C>GCA352149272SCN5Ac.3724G>C (p.Asp1242His)
c.3727G>C (p.Asp1243His)
c.3565G>C (p.Asp1189His)
c.3598G>C (p.Asp1200His)
3g.38566522C>TCA017472SCN5Ac.3724G>A (p.Asp1242Asn)
c.3727G>A (p.Asp1243Asn)
c.3565G>A (p.Asp1189Asn)
c.3598G>A (p.Asp1200Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38566523G>ACA062223SCN5Ac.3723C>T (p.Ala1241=)
c.3726C>T (p.Ala1242=)
c.3564C>T (p.Ala1188=)
c.3597C>T (p.Ala1199=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38566523G>CCA433136863SCN5Ac.3723C>G (p.Ala1241=)
c.3726C>G (p.Ala1242=)
c.3564C>G (p.Ala1188=)
c.3597C>G (p.Ala1199=)
 ClinVar
3g.38566523G=CA1358569709SCN5Ac.3723C= (p.Ala1241=)
c.3726C= (p.Ala1242=)
c.3564C= (p.Ala1188=)
c.3597C= (p.Ala1199=)
3g.38566523G>TCA433136865SCN5Ac.3723C>A (p.Ala1241=)
c.3726C>A (p.Ala1242=)
c.3564C>A (p.Ala1188=)
c.3597C>A (p.Ala1199=)
3g.38566524G>ACA352149277SCN5Ac.3722C>T (p.Ala1241Val)
c.3725C>T (p.Ala1242Val)
c.3563C>T (p.Ala1188Val)
c.3596C>T (p.Ala1199Val)
 COSMIC COSMIC COSMIC
3g.38566524G>CCA352149279SCN5Ac.3722C>G (p.Ala1241Gly)
c.3725C>G (p.Ala1242Gly)
c.3563C>G (p.Ala1188Gly)
c.3596C>G (p.Ala1199Gly)
 gnomAD v4
3g.38566524G>TCA352149280SCN5Ac.3722C>A (p.Ala1241Asp)
c.3725C>A (p.Ala1242Asp)
c.3563C>A (p.Ala1188Asp)
c.3596C>A (p.Ala1199Asp)
3g.38566525C>ACA352149282SCN5Ac.3721G>T (p.Ala1241Ser)
c.3724G>T (p.Ala1242Ser)
c.3562G>T (p.Ala1188Ser)
c.3595G>T (p.Ala1199Ser)
3g.38566525C>GCA352149284SCN5Ac.3721G>C (p.Ala1241Pro)
c.3724G>C (p.Ala1242Pro)
c.3562G>C (p.Ala1188Pro)
c.3595G>C (p.Ala1199Pro)
3g.38566525C>TCA352149285SCN5Ac.3721G>A (p.Ala1241Thr)
c.3724G>A (p.Ala1242Thr)
c.3562G>A (p.Ala1188Thr)
c.3595G>A (p.Ala1199Thr)
3g.38566526A=CA1358569713SCN5Ac.3720T= (p.Tyr1240=)
c.3723T= (p.Tyr1241=)
c.3561T= (p.Tyr1187=)
c.3594T= (p.Tyr1198=)
3g.38566526A>CCA352149286SCN5Ac.3720T>G (p.Tyr1240Ter)
c.3723T>G (p.Tyr1241Ter)
c.3561T>G (p.Tyr1187Ter)
c.3594T>G (p.Tyr1198Ter)
3g.38566526A>GCA433136869SCN5Ac.3720T>C (p.Tyr1240=)
c.3723T>C (p.Tyr1241=)
c.3561T>C (p.Tyr1187=)
c.3594T>C (p.Tyr1198=)
 dbSNP gnomAD v2 gnomAD v4
3g.38566526A>TCA352149287SCN5Ac.3720T>A (p.Tyr1240Ter)
c.3723T>A (p.Tyr1241Ter)
c.3561T>A (p.Tyr1187Ter)
c.3594T>A (p.Tyr1198Ter)
3g.38566527T>ACA352149292SCN5Ac.3719A>T (p.Tyr1240Phe)
c.3722A>T (p.Tyr1241Phe)
c.3560A>T (p.Tyr1187Phe)
c.3593A>T (p.Tyr1198Phe)
3g.38566527T>CCA352149290SCN5Ac.3719A>G (p.Tyr1240Cys)
c.3722A>G (p.Tyr1241Cys)
c.3560A>G (p.Tyr1187Cys)
c.3593A>G (p.Tyr1198Cys)
 ClinVar dbSNP gnomAD v4
3g.38566527T>GCA017466SCN5Ac.3719A>C (p.Tyr1240Ser)
c.3722A>C (p.Tyr1241Ser)
c.3560A>C (p.Tyr1187Ser)
c.3593A>C (p.Tyr1198Ser)
 ClinVar dbSNP gnomAD v4
3g.38566527T=CA1358569716SCN5Ac.3719A= (p.Tyr1240=)
c.3722A= (p.Tyr1241=)
c.3560A= (p.Tyr1187=)
c.3593A= (p.Tyr1198=)
3g.38566528A>CCA352149294SCN5Ac.3718T>G (p.Tyr1240Asp)
c.3721T>G (p.Tyr1241Asp)
c.3559T>G (p.Tyr1187Asp)
c.3592T>G (p.Tyr1198Asp)
3g.38566528A>GCA352149296SCN5Ac.3718T>C (p.Tyr1240His)
c.3721T>C (p.Tyr1241His)
c.3559T>C (p.Tyr1187His)
c.3592T>C (p.Tyr1198His)
3g.38566528A>TCA352149298SCN5Ac.3718T>A (p.Tyr1240Asn)
c.3721T>A (p.Tyr1241Asn)
c.3559T>A (p.Tyr1187Asn)
c.3592T>A (p.Tyr1198Asn)
 COSMIC
3g.38566529C>ACA352149300SCN5Ac.3717G>T (p.Glu1239Asp)
c.3720G>T (p.Glu1240Asp)
c.3558G>T (p.Glu1186Asp)
c.3591G>T (p.Glu1197Asp)
3g.38566529C>GCA352149301SCN5Ac.3717G>C (p.Glu1239Asp)
c.3720G>C (p.Glu1240Asp)
c.3558G>C (p.Glu1186Asp)
c.3591G>C (p.Glu1197Asp)
3g.38566529C>TCA433136878SCN5Ac.3717G>A (p.Glu1239=)
c.3720G>A (p.Glu1240=)
c.3558G>A (p.Glu1186=)
c.3591G>A (p.Glu1197=)
3g.38566530T>ACA352149304SCN5Ac.3716A>T (p.Glu1239Val)
c.3719A>T (p.Glu1240Val)
c.3557A>T (p.Glu1186Val)
c.3590A>T (p.Glu1197Val)
3g.38566530T>CCA352149306SCN5Ac.3716A>G (p.Glu1239Gly)
c.3719A>G (p.Glu1240Gly)
c.3557A>G (p.Glu1186Gly)
c.3590A>G (p.Glu1197Gly)
3g.38566530T>GCA352149308SCN5Ac.3716A>C (p.Glu1239Ala)
c.3719A>C (p.Glu1240Ala)
c.3557A>C (p.Glu1186Ala)
c.3590A>C (p.Glu1197Ala)
 dbSNP
3g.38566530T=CA1358569721SCN5Ac.3716A= (p.Glu1239=)
c.3719A= (p.Glu1240=)
c.3557A= (p.Glu1186=)
c.3590A= (p.Glu1197=)
3g.38566531C>ACA352149310SCN5Ac.3715G>T (p.Glu1239Ter)
c.3718G>T (p.Glu1240Ter)
c.3556G>T (p.Glu1186Ter)
c.3589G>T (p.Glu1197Ter)
 dbSNP
3g.38566531C=CA1358569731SCN5Ac.3715G= (p.Glu1239=)
c.3718G= (p.Glu1240=)
c.3556G= (p.Glu1186=)
c.3589G= (p.Glu1197=)
3g.38566531C>GCA017461SCN5Ac.3715G>C (p.Glu1239Gln)
c.3718G>C (p.Glu1240Gln)
c.3556G>C (p.Glu1186Gln)
c.3589G>C (p.Glu1197Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38566531C>TCA352149312SCN5Ac.3715G>A (p.Glu1239Lys)
c.3718G>A (p.Glu1240Lys)
c.3556G>A (p.Glu1186Lys)
c.3589G>A (p.Glu1197Lys)
3g.38566532A>CCA433136881SCN5Ac.3714T>G (p.Leu1238=)
c.3717T>G (p.Leu1239=)
c.3555T>G (p.Leu1185=)
c.3588T>G (p.Leu1196=)
 gnomAD v4
3g.38566532A>GCA433136884SCN5Ac.3714T>C (p.Leu1238=)
c.3717T>C (p.Leu1239=)
c.3555T>C (p.Leu1185=)
c.3588T>C (p.Leu1196=)
3g.38566532A>TCA433136883SCN5Ac.3714T>A (p.Leu1238=)
c.3717T>A (p.Leu1239=)
c.3555T>A (p.Leu1185=)
c.3588T>A (p.Leu1196=)
3g.38566533delCA2577553238SCN5Ac.3714del (p.Glu1239SerfsTer?)
c.3717del (p.Glu1240SerfsTer?)
c.3555del (p.Glu1186SerfsTer?)
c.3588del (p.Glu1197SerfsTer?)
3g.38566533A=CA1358569733SCN5Ac.3713T= (p.Leu1238=)
c.3716T= (p.Leu1239=)
c.3554T= (p.Leu1185=)
c.3587T= (p.Leu1196=)
3g.38566533A>CCA352149314SCN5Ac.3713T>G (p.Leu1238Arg)
c.3716T>G (p.Leu1239Arg)
c.3554T>G (p.Leu1185Arg)
c.3587T>G (p.Leu1196Arg)
3g.38566533A>GCA017455SCN5Ac.3713T>C (p.Leu1238Pro)
c.3716T>C (p.Leu1239Pro)
c.3554T>C (p.Leu1185Pro)
c.3587T>C (p.Leu1196Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38566533A>TCA352149316SCN5Ac.3713T>A (p.Leu1238His)
c.3716T>A (p.Leu1239His)
c.3554T>A (p.Leu1185His)
c.3587T>A (p.Leu1196His)
3g.38566534G>ACA352149322SCN5Ac.3712C>T (p.Leu1238Phe)
c.3715C>T (p.Leu1239Phe)
c.3553C>T (p.Leu1185Phe)
c.3586C>T (p.Leu1196Phe)
 gnomAD v4
3g.38566534G>CCA352149320SCN5Ac.3712C>G (p.Leu1238Val)
c.3715C>G (p.Leu1239Val)
c.3553C>G (p.Leu1185Val)
c.3586C>G (p.Leu1196Val)
3g.38566534G>TCA352149319SCN5Ac.3712C>A (p.Leu1238Ile)
c.3715C>A (p.Leu1239Ile)
c.3553C>A (p.Leu1185Ile)
c.3586C>A (p.Leu1196Ile)
3g.38566535C>ACA433136888SCN5Ac.3711G>T (p.Leu1237=)
c.3714G>T (p.Leu1238=)
c.3552G>T (p.Leu1184=)
c.3585G>T (p.Leu1195=)
3g.38566535C=CA1358569738SCN5Ac.3711G= (p.Leu1237=)
c.3714G= (p.Leu1238=)
c.3552G= (p.Leu1184=)
c.3585G= (p.Leu1195=)
3g.38566535C>GCA433136890SCN5Ac.3711G>C (p.Leu1237=)
c.3714G>C (p.Leu1238=)
c.3552G>C (p.Leu1184=)
c.3585G>C (p.Leu1195=)
3g.38566535C>TCA433136889SCN5Ac.3711G>A (p.Leu1237=)
c.3714G>A (p.Leu1238=)
c.3552G>A (p.Leu1184=)
c.3585G>A (p.Leu1195=)
 dbSNP gnomAD v4
3g.38566536A>CCA352149325SCN5Ac.3710T>G (p.Leu1237Arg)
c.3713T>G (p.Leu1238Arg)
c.3551T>G (p.Leu1184Arg)
c.3584T>G (p.Leu1195Arg)
3g.38566536A>GCA352149327SCN5Ac.3710T>C (p.Leu1237Pro)
c.3713T>C (p.Leu1238Pro)
c.3551T>C (p.Leu1184Pro)
c.3584T>C (p.Leu1195Pro)
3g.38566536A>TCA352149329SCN5Ac.3710T>A (p.Leu1237Gln)
c.3713T>A (p.Leu1238Gln)
c.3551T>A (p.Leu1184Gln)
c.3584T>A (p.Leu1195Gln)
3g.38566537G>ACA433136892SCN5Ac.3709C>T (p.Leu1237=)
c.3712C>T (p.Leu1238=)
c.3550C>T (p.Leu1184=)
c.3583C>T (p.Leu1195=)
3g.38566537G>CCA352149331SCN5Ac.3709C>G (p.Leu1237Val)
c.3712C>G (p.Leu1238Val)
c.3550C>G (p.Leu1184Val)
c.3583C>G (p.Leu1195Val)
3g.38566537G>TCA352149333SCN5Ac.3709C>A (p.Leu1237Met)
c.3712C>A (p.Leu1238Met)
c.3550C>A (p.Leu1184Met)
c.3583C>A (p.Leu1195Met)
 gnomAD v4
3g.38566538A>CCA433136894SCN5Ac.3708T>G (p.Val1236=)
c.3711T>G (p.Val1237=)
c.3549T>G (p.Val1183=)
c.3582T>G (p.Val1194=)
3g.38566538A>GCA433136895SCN5Ac.3708T>C (p.Val1236=)
c.3711T>C (p.Val1237=)
c.3549T>C (p.Val1183=)
c.3582T>C (p.Val1194=)
3g.38566538A>TCA433136896SCN5Ac.3708T>A (p.Val1236=)
c.3711T>A (p.Val1237=)
c.3549T>A (p.Val1183=)
c.3582T>A (p.Val1194=)
3g.38566539A>CCA352149335SCN5Ac.3707T>G (p.Val1236Gly)
c.3710T>G (p.Val1237Gly)
c.3548T>G (p.Val1183Gly)
c.3581T>G (p.Val1194Gly)
3g.38566539A>GCA352149337SCN5Ac.3707T>C (p.Val1236Ala)
c.3710T>C (p.Val1237Ala)
c.3548T>C (p.Val1183Ala)
c.3581T>C (p.Val1194Ala)
 ClinVar dbSNP gnomAD v4
3g.38566539A>TCA352149339SCN5Ac.3707T>A (p.Val1236Asp)
c.3710T>A (p.Val1237Asp)
c.3548T>A (p.Val1183Asp)
c.3581T>A (p.Val1194Asp)
3g.38566540C>ACA352149341SCN5Ac.3706G>T (p.Val1236Phe)
c.3709G>T (p.Val1237Phe)
c.3547G>T (p.Val1183Phe)
c.3580G>T (p.Val1194Phe)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38566540C=CA1358569743SCN5Ac.3706G= (p.Val1236=)
c.3709G= (p.Val1237=)
c.3547G= (p.Val1183=)
c.3580G= (p.Val1194=)
3g.38566540C>GCA352149343SCN5Ac.3706G>C (p.Val1236Leu)
c.3709G>C (p.Val1237Leu)
c.3547G>C (p.Val1183Leu)
c.3580G>C (p.Val1194Leu)
 gnomAD v4
3g.38566540C>TCA017449SCN5Ac.3706G>A (p.Val1236Ile)
c.3709G>A (p.Val1237Ile)
c.3547G>A (p.Val1183Ile)
c.3580G>A (p.Val1194Ile)
 ClinVar dbSNP gnomAD v4
3g.38566541C>ACA017441SCN5Ac.3705G>T (p.Lys1235Asn)
c.3708G>T (p.Lys1236Asn)
c.3546G>T (p.Lys1182Asn)
c.3579G>T (p.Lys1193Asn)
 ClinVar dbSNP gnomAD v4
3g.38566541C=CA1358569748SCN5Ac.3705G= (p.Lys1235=)
c.3708G= (p.Lys1236=)
c.3546G= (p.Lys1182=)
c.3579G= (p.Lys1193=)
3g.38566541C>GCA352149346SCN5Ac.3705G>C (p.Lys1235Asn)
c.3708G>C (p.Lys1236Asn)
c.3546G>C (p.Lys1182Asn)
c.3579G>C (p.Lys1193Asn)
3g.38566541C>TCA433136902SCN5Ac.3705G>A (p.Lys1235=)
c.3708G>A (p.Lys1236=)
c.3546G>A (p.Lys1182=)
c.3579G>A (p.Lys1193=)
 gnomAD v4
3g.38566542T>ACA352149351SCN5Ac.3704A>T (p.Lys1235Met)
c.3707A>T (p.Lys1236Met)
c.3545A>T (p.Lys1182Met)
c.3578A>T (p.Lys1193Met)
3g.38566542T>CCA017434SCN5Ac.3704A>G (p.Lys1235Arg)
c.3707A>G (p.Lys1236Arg)
c.3545A>G (p.Lys1182Arg)
c.3578A>G (p.Lys1193Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38566542T>GCA352149348SCN5Ac.3704A>C (p.Lys1235Thr)
c.3707A>C (p.Lys1236Thr)
c.3545A>C (p.Lys1182Thr)
c.3578A>C (p.Lys1193Thr)
3g.38566542T=CA1358569753SCN5Ac.3704A= (p.Lys1235=)
c.3707A= (p.Lys1236=)
c.3545A= (p.Lys1182=)
c.3578A= (p.Lys1193=)
3g.38566543T>ACA352149353SCN5Ac.3703A>T (p.Lys1235Ter)
c.3706A>T (p.Lys1236Ter)
c.3544A>T (p.Lys1182Ter)
c.3577A>T (p.Lys1193Ter)
 dbSNP
3g.38566543T>CCA352149355SCN5Ac.3703A>G (p.Lys1235Glu)
c.3706A>G (p.Lys1236Glu)
c.3544A>G (p.Lys1182Glu)
c.3577A>G (p.Lys1193Glu)
3g.38566543T>GCA352149357SCN5Ac.3703A>C (p.Lys1235Gln)
c.3706A>C (p.Lys1236Gln)
c.3544A>C (p.Lys1182Gln)
c.3577A>C (p.Lys1193Gln)
3g.38566543T=CA1358569757SCN5Ac.3703A= (p.Lys1235=)
c.3706A= (p.Lys1236=)
c.3544A= (p.Lys1182=)
c.3577A= (p.Lys1193=)
3g.38566544G>ACA433136906SCN5Ac.3702C>T (p.Ile1234=)
c.3705C>T (p.Ile1235=)
c.3543C>T (p.Ile1181=)
c.3576C>T (p.Ile1192=)
3g.38566544G>CCA352149359SCN5Ac.3702C>G (p.Ile1234Met)
c.3705C>G (p.Ile1235Met)
c.3543C>G (p.Ile1181Met)
c.3576C>G (p.Ile1192Met)
3g.38566544G>TCA433136907SCN5Ac.3702C>A (p.Ile1234=)
c.3705C>A (p.Ile1235=)
c.3543C>A (p.Ile1181=)
c.3576C>A (p.Ile1192=)
3g.38566545A>CCA352149361SCN5Ac.3701T>G (p.Ile1234Ser)
c.3704T>G (p.Ile1235Ser)
c.3542T>G (p.Ile1181Ser)
c.3575T>G (p.Ile1192Ser)
3g.38566545A>GCA352149364SCN5Ac.3701T>C (p.Ile1234Thr)
c.3704T>C (p.Ile1235Thr)
c.3542T>C (p.Ile1181Thr)
c.3575T>C (p.Ile1192Thr)
3g.38566545A>TCA352149365SCN5Ac.3701T>A (p.Ile1234Asn)
c.3704T>A (p.Ile1235Asn)
c.3542T>A (p.Ile1181Asn)
c.3575T>A (p.Ile1192Asn)
3g.38566546T>ACA352149366SCN5Ac.3700A>T (p.Ile1234Phe)
c.3703A>T (p.Ile1235Phe)
c.3541A>T (p.Ile1181Phe)
c.3574A>T (p.Ile1192Phe)
 gnomAD v4
3g.38566546T>CCA352149367SCN5Ac.3700A>G (p.Ile1234Val)
c.3703A>G (p.Ile1235Val)
c.3541A>G (p.Ile1181Val)
c.3574A>G (p.Ile1192Val)
3g.38566546T>GCA352149369SCN5Ac.3700A>C (p.Ile1234Leu)
c.3703A>C (p.Ile1235Leu)
c.3541A>C (p.Ile1181Leu)
c.3574A>C (p.Ile1192Leu)
3g.38566547G>ACA433136913SCN5Ac.3699C>T (p.Thr1233=)
c.3702C>T (p.Thr1234=)
c.3540C>T (p.Thr1180=)
c.3573C>T (p.Thr1191=)
 gnomAD v4
3g.38566547G>CCA433136915SCN5Ac.3699C>G (p.Thr1233=)
c.3702C>G (p.Thr1234=)
c.3540C>G (p.Thr1180=)
c.3573C>G (p.Thr1191=)
3g.38566547G>TCA433136916SCN5Ac.3699C>A (p.Thr1233=)
c.3702C>A (p.Thr1234=)
c.3540C>A (p.Thr1180=)
c.3573C>A (p.Thr1191=)
3g.38566548G>ACA352149371SCN5Ac.3698C>T (p.Thr1233Ile)
c.3701C>T (p.Thr1234Ile)
c.3539C>T (p.Thr1180Ile)
c.3572C>T (p.Thr1191Ile)
 ClinVar
3g.38566548G>CCA352149372SCN5Ac.3698C>G (p.Thr1233Ser)
c.3701C>G (p.Thr1234Ser)
c.3539C>G (p.Thr1180Ser)
c.3572C>G (p.Thr1191Ser)
3g.38566548G>TCA352149373SCN5Ac.3698C>A (p.Thr1233Asn)
c.3701C>A (p.Thr1234Asn)
c.3539C>A (p.Thr1180Asn)
c.3572C>A (p.Thr1191Asn)
3g.38566549T>ACA352149391SCN5Ac.3697A>T (p.Thr1233Ser)
c.3700A>T (p.Thr1234Ser)
c.3538A>T (p.Thr1180Ser)
c.3571A>T (p.Thr1191Ser)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38566549T>CCA352149392SCN5Ac.3697A>G (p.Thr1233Ala)
c.3700A>G (p.Thr1234Ala)
c.3538A>G (p.Thr1180Ala)
c.3571A>G (p.Thr1191Ala)
3g.38566549T>GCA352149382SCN5Ac.3697A>C (p.Thr1233Pro)
c.3700A>C (p.Thr1234Pro)
c.3538A>C (p.Thr1180Pro)
c.3571A>C (p.Thr1191Pro)
3g.38566549T=CA1358569759SCN5Ac.3697A= (p.Thr1233=)
c.3700A= (p.Thr1234=)
c.3538A= (p.Thr1180=)
c.3571A= (p.Thr1191=)
3g.38566550C>ACA352149393SCN5Ac.3696G>T (p.Lys1232Asn)
c.3699G>T (p.Lys1233Asn)
c.3537G>T (p.Lys1179Asn)
c.3570G>T (p.Lys1190Asn)
 gnomAD v4
3g.38566550C>GCA352149394SCN5Ac.3696G>C (p.Lys1232Asn)
c.3699G>C (p.Lys1233Asn)
c.3537G>C (p.Lys1179Asn)
c.3570G>C (p.Lys1190Asn)
3g.38566550C>TCA433136922SCN5Ac.3696G>A (p.Lys1232=)
c.3699G>A (p.Lys1233=)
c.3537G>A (p.Lys1179=)
c.3570G>A (p.Lys1190=)
 COSMIC COSMIC COSMIC
3g.38566551T>ACA352149395SCN5Ac.3695A>T (p.Lys1232Met)
c.3698A>T (p.Lys1233Met)
c.3536A>T (p.Lys1179Met)
c.3569A>T (p.Lys1190Met)
3g.38566551T>CCA352149396SCN5Ac.3695A>G (p.Lys1232Arg)
c.3698A>G (p.Lys1233Arg)
c.3536A>G (p.Lys1179Arg)
c.3569A>G (p.Lys1190Arg)
3g.38566551T>GCA352149397SCN5Ac.3695A>C (p.Lys1232Thr)
c.3698A>C (p.Lys1233Thr)
c.3536A>C (p.Lys1179Thr)
c.3569A>C (p.Lys1190Thr)
3g.38566552T>ACA352149398SCN5Ac.3694A>T (p.Lys1232Ter)
c.3697A>T (p.Lys1233Ter)
c.3535A>T (p.Lys1179Ter)
c.3568A>T (p.Lys1190Ter)
 ClinVar dbSNP
3g.38566552T>CCA352149399SCN5Ac.3694A>G (p.Lys1232Glu)
c.3697A>G (p.Lys1233Glu)
c.3535A>G (p.Lys1179Glu)
c.3568A>G (p.Lys1190Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38566552T>GCA352149401SCN5Ac.3694A>C (p.Lys1232Gln)
c.3697A>C (p.Lys1233Gln)
c.3535A>C (p.Lys1179Gln)
c.3568A>C (p.Lys1190Gln)
3g.38566552T=CA1358569763SCN5Ac.3694A= (p.Lys1232=)
c.3697A= (p.Lys1233=)
c.3535A= (p.Lys1179=)
c.3568A= (p.Lys1190=)
3g.38566553C>ACA433136932SCN5Ac.3693G>T (p.Arg1231=)
c.3696G>T (p.Arg1232=)
c.3534G>T (p.Arg1178=)
c.3567G>T (p.Arg1189=)
3g.38566553C>GCA433136930SCN5Ac.3693G>C (p.Arg1231=)
c.3696G>C (p.Arg1232=)
c.3534G>C (p.Arg1178=)
c.3567G>C (p.Arg1189=)
3g.38566553C>TCA433136928SCN5Ac.3693G>A (p.Arg1231=)
c.3696G>A (p.Arg1232=)
c.3534G>A (p.Arg1178=)
c.3567G>A (p.Arg1189=)
 gnomAD v4
3g.38566554delCA2580069778SCN5Ac.3693del (p.Lys1232ArgfsTer?)
c.3696del (p.Lys1233ArgfsTer?)
c.3534del (p.Lys1179ArgfsTer?)
c.3567del (p.Lys1190ArgfsTer?)
 ClinVar
3g.38566554C>ACA352149402SCN5Ac.3692G>T (p.Arg1231Leu)
c.3695G>T (p.Arg1232Leu)
c.3533G>T (p.Arg1178Leu)
c.3566G>T (p.Arg1189Leu)
3g.38566554C=CA1358569768SCN5Ac.3692G= (p.Arg1231=)
c.3695G= (p.Arg1232=)
c.3533G= (p.Arg1178=)
c.3566G= (p.Arg1189=)
3g.38566554C>GCA352149403SCN5Ac.3692G>C (p.Arg1231Pro)
c.3695G>C (p.Arg1232Pro)
c.3533G>C (p.Arg1178Pro)
c.3566G>C (p.Arg1189Pro)
3g.38566554C>TCA017422SCN5Ac.3692G>A (p.Arg1231Gln)
c.3695G>A (p.Arg1232Gln)
c.3533G>A (p.Arg1178Gln)
c.3566G>A (p.Arg1189Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38566555G>ACA017416SCN5Ac.3691C>T (p.Arg1231Trp)
c.3694C>T (p.Arg1232Trp)
c.3532C>T (p.Arg1178Trp)
c.3565C>T (p.Arg1189Trp)
 ClinVar dbSNP gnomAD v4
3g.38566555G>CCA352149406SCN5Ac.3691C>G (p.Arg1231Gly)
c.3694C>G (p.Arg1232Gly)
c.3532C>G (p.Arg1178Gly)
c.3565C>G (p.Arg1189Gly)
3g.38566555G=CA1358569777SCN5Ac.3691C= (p.Arg1231=)
c.3694C= (p.Arg1232=)
c.3532C= (p.Arg1178=)
c.3565C= (p.Arg1189=)
3g.38566555G>TCA433136933SCN5Ac.3691C>A (p.Arg1231=)
c.3694C>A (p.Arg1232=)
c.3532C>A (p.Arg1178=)
c.3565C>A (p.Arg1189=)
 COSMIC COSMIC COSMIC
3g.38566556C>ACA352149407SCN5Ac.3690G>T (p.Glu1230Asp)
c.3693G>T (p.Glu1231Asp)
c.3531G>T (p.Glu1177Asp)
c.3564G>T (p.Glu1188Asp)
3g.38566556C=CA1358569781SCN5Ac.3690G= (p.Glu1230=)
c.3693G= (p.Glu1231=)
c.3531G= (p.Glu1177=)
c.3564G= (p.Glu1188=)
3g.38566556C>GCA352149409SCN5Ac.3690G>C (p.Glu1230Asp)
c.3693G>C (p.Glu1231Asp)
c.3531G>C (p.Glu1177Asp)
c.3564G>C (p.Glu1188Asp)
3g.38566556C>TCA433136934SCN5Ac.3690G>A (p.Glu1230=)
c.3693G>A (p.Glu1231=)
c.3531G>A (p.Glu1177=)
c.3564G>A (p.Glu1188=)
 dbSNP
3g.38566557T>ACA352149415SCN5Ac.3689A>T (p.Glu1230Val)
c.3692A>T (p.Glu1231Val)
c.3530A>T (p.Glu1177Val)
c.3563A>T (p.Glu1188Val)
3g.38566557T>CCA352149411SCN5Ac.3689A>G (p.Glu1230Gly)
c.3692A>G (p.Glu1231Gly)
c.3530A>G (p.Glu1177Gly)
c.3563A>G (p.Glu1188Gly)
 gnomAD v4
3g.38566557T>GCA352149413SCN5Ac.3689A>C (p.Glu1230Ala)
c.3692A>C (p.Glu1231Ala)
c.3530A>C (p.Glu1177Ala)
c.3563A>C (p.Glu1188Ala)
 ClinVar dbSNP
3g.38566557T=CA1358569785SCN5Ac.3689A= (p.Glu1230=)
c.3692A= (p.Glu1231=)
c.3530A= (p.Glu1177=)
c.3563A= (p.Glu1188=)
3g.38566558C>ACA352149417SCN5Ac.3688G>T (p.Glu1230Ter)
c.3691G>T (p.Glu1231Ter)
c.3529G>T (p.Glu1177Ter)
c.3562G>T (p.Glu1188Ter)
 ClinVar dbSNP gnomAD v4
3g.38566558C=CA1358569801SCN5Ac.3688G= (p.Glu1230=)
c.3691G= (p.Glu1231=)
c.3529G= (p.Glu1177=)
c.3562G= (p.Glu1188=)
3g.38566558C>GCA352149419SCN5Ac.3688G>C (p.Glu1230Gln)
c.3691G>C (p.Glu1231Gln)
c.3529G>C (p.Glu1177Gln)
c.3562G>C (p.Glu1188Gln)
 ClinVar dbSNP
3g.38566558C>TCA017410SCN5Ac.3688G>A (p.Glu1230Lys)
c.3691G>A (p.Glu1231Lys)
c.3529G>A (p.Glu1177Lys)
c.3562G>A (p.Glu1188Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
3g.38566559C>ACA352149421SCN5Ac.3687G>T (p.Glu1229Asp)
c.3690G>T (p.Glu1230Asp)
c.3528G>T (p.Glu1176Asp)
c.3561G>T (p.Glu1187Asp)
3g.38566559C>GCA352149422SCN5Ac.3687G>C (p.Glu1229Asp)
c.3690G>C (p.Glu1230Asp)
c.3528G>C (p.Glu1176Asp)
c.3561G>C (p.Glu1187Asp)
3g.38566559C>TCA433136940SCN5Ac.3687G>A (p.Glu1229=)
c.3690G>A (p.Glu1230=)
c.3528G>A (p.Glu1176=)
c.3561G>A (p.Glu1187=)
3g.38566560T>ACA352149423SCN5Ac.3686A>T (p.Glu1229Val)
c.3689A>T (p.Glu1230Val)
c.3527A>T (p.Glu1176Val)
c.3560A>T (p.Glu1187Val)
3g.38566560T>CCA352149425SCN5Ac.3686A>G (p.Glu1229Gly)
c.3689A>G (p.Glu1230Gly)
c.3527A>G (p.Glu1176Gly)
c.3560A>G (p.Glu1187Gly)
3g.38566560T>GCA352149426SCN5Ac.3686A>C (p.Glu1229Ala)
c.3689A>C (p.Glu1230Ala)
c.3527A>C (p.Glu1176Ala)
c.3560A>C (p.Glu1187Ala)
3g.38566561C>ACA352149427SCN5Ac.3685G>T (p.Glu1229Ter)
c.3688G>T (p.Glu1230Ter)
c.3526G>T (p.Glu1176Ter)
c.3559G>T (p.Glu1187Ter)
 dbSNP
3g.38566561C=CA1358569808SCN5Ac.3685G= (p.Glu1229=)
c.3688G= (p.Glu1230=)
c.3526G= (p.Glu1176=)
c.3559G= (p.Glu1187=)
3g.38566561C>GCA352149428SCN5Ac.3685G>C (p.Glu1229Gln)
c.3688G>C (p.Glu1230Gln)
c.3526G>C (p.Glu1176Gln)
c.3559G>C (p.Glu1187Gln)
3g.38566561C>TCA062201SCN5Ac.3685G>A (p.Glu1229Lys)
c.3688G>A (p.Glu1230Lys)
c.3526G>A (p.Glu1176Lys)
c.3559G>A (p.Glu1187Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38566562T>ACA433136946SCN5Ac.3684A>T (p.Leu1228=)
c.3687A>T (p.Leu1229=)
c.3525A>T (p.Leu1175=)
c.3558A>T (p.Leu1186=)
3g.38566562T>CCA433136947SCN5Ac.3684A>G (p.Leu1228=)
c.3687A>G (p.Leu1229=)
c.3525A>G (p.Leu1175=)
c.3558A>G (p.Leu1186=)
 ClinVar dbSNP
3g.38566562T>GCA433136949SCN5Ac.3684A>C (p.Leu1228=)
c.3687A>C (p.Leu1229=)
c.3525A>C (p.Leu1175=)
c.3558A>C (p.Leu1186=)
3g.38566563A>CCA352149436SCN5Ac.3683T>G (p.Leu1228Arg)
c.3686T>G (p.Leu1229Arg)
c.3524T>G (p.Leu1175Arg)
c.3557T>G (p.Leu1186Arg)
3g.38566563A>GCA352149433SCN5Ac.3683T>C (p.Leu1228Pro)
c.3686T>C (p.Leu1229Pro)
c.3524T>C (p.Leu1175Pro)
c.3557T>C (p.Leu1186Pro)
3g.38566563A>TCA352149432SCN5Ac.3683T>A (p.Leu1228Gln)
c.3686T>A (p.Leu1229Gln)
c.3524T>A (p.Leu1175Gln)
c.3557T>A (p.Leu1186Gln)
 gnomAD v4
3g.38566564G>ACA433136950SCN5Ac.3682C>T (p.Leu1228=)
c.3685C>T (p.Leu1229=)
c.3523C>T (p.Leu1175=)
c.3556C>T (p.Leu1186=)
 ClinVar
3g.38566564G>CCA352149438SCN5Ac.3682C>G (p.Leu1228Val)
c.3685C>G (p.Leu1229Val)
c.3523C>G (p.Leu1175Val)
c.3556C>G (p.Leu1186Val)
3g.38566564G>TCA352149439SCN5Ac.3682C>A (p.Leu1228Ile)
c.3685C>A (p.Leu1229Ile)
c.3523C>A (p.Leu1175Ile)
c.3556C>A (p.Leu1186Ile)
3g.38566565G>ACA433136953SCN5Ac.3681C>T (p.Tyr1227=)
c.3684C>T (p.Tyr1228=)
c.3522C>T (p.Tyr1174=)
c.3555C>T (p.Tyr1185=)
3g.38566565G>CCA352149443SCN5Ac.3681C>G (p.Tyr1227Ter)
c.3684C>G (p.Tyr1228Ter)
c.3522C>G (p.Tyr1174Ter)
c.3555C>G (p.Tyr1185Ter)
 ClinVar dbSNP
3g.38566565G=CA1358569811SCN5Ac.3681C= (p.Tyr1227=)
c.3684C= (p.Tyr1228=)
c.3522C= (p.Tyr1174=)
c.3555C= (p.Tyr1185=)
3g.38566565G>TCA352149444SCN5Ac.3681C>A (p.Tyr1227Ter)
c.3684C>A (p.Tyr1228Ter)
c.3522C>A (p.Tyr1174Ter)
c.3555C>A (p.Tyr1185Ter)
3g.38566566T>ACA352149448SCN5Ac.3680A>T (p.Tyr1227Phe)
c.3683A>T (p.Tyr1228Phe)
c.3521A>T (p.Tyr1174Phe)
c.3554A>T (p.Tyr1185Phe)
 dbSNP gnomAD v2 gnomAD v4
3g.38566566T>CCA062194SCN5Ac.3680A>G (p.Tyr1227Cys)
c.3683A>G (p.Tyr1228Cys)
c.3521A>G (p.Tyr1174Cys)
c.3554A>G (p.Tyr1185Cys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38566566T>GCA352149450SCN5Ac.3680A>C (p.Tyr1227Ser)
c.3683A>C (p.Tyr1228Ser)
c.3521A>C (p.Tyr1174Ser)
c.3554A>C (p.Tyr1185Ser)
 ClinVar dbSNP gnomAD v4
3g.38566566T=CA1358569819SCN5Ac.3680A= (p.Tyr1227=)
c.3683A= (p.Tyr1228=)
c.3521A= (p.Tyr1174=)
c.3554A= (p.Tyr1185=)
3g.38566567A=CA1358569827SCN5Ac.3679T= (p.Tyr1227=)
c.3682T= (p.Tyr1228=)
c.3520T= (p.Tyr1174=)
c.3553T= (p.Tyr1185=)
3g.38566567A>CCA352149452SCN5Ac.3679T>G (p.Tyr1227Asp)
c.3682T>G (p.Tyr1228Asp)
c.3520T>G (p.Tyr1174Asp)
c.3553T>G (p.Tyr1185Asp)
3g.38566567A>GCA017405SCN5Ac.3679T>C (p.Tyr1227His)
c.3682T>C (p.Tyr1228His)
c.3520T>C (p.Tyr1174His)
c.3553T>C (p.Tyr1185His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38566567A>TCA352149454SCN5Ac.3679T>A (p.Tyr1227Asn)
c.3682T>A (p.Tyr1228Asn)
c.3520T>A (p.Tyr1174Asn)
c.3553T>A (p.Tyr1185Asn)
3g.38566568G>ACA433136963SCN5Ac.3678C>T (p.Ile1226=)
c.3681C>T (p.Ile1227=)
c.3519C>T (p.Ile1173=)
c.3552C>T (p.Ile1184=)
3g.38566568G>CCA352149456SCN5Ac.3678C>G (p.Ile1226Met)
c.3681C>G (p.Ile1227Met)
c.3519C>G (p.Ile1173Met)
c.3552C>G (p.Ile1184Met)
3g.38566568G>TCA433136960SCN5Ac.3678C>A (p.Ile1226=)
c.3681C>A (p.Ile1227=)
c.3519C>A (p.Ile1173=)
c.3552C>A (p.Ile1184=)
 ClinVar gnomAD v4
3g.38566569A>CCA352149459SCN5Ac.3677T>G (p.Ile1226Ser)
c.3680T>G (p.Ile1227Ser)
c.3518T>G (p.Ile1173Ser)
c.3551T>G (p.Ile1184Ser)
3g.38566569A>GCA352149461SCN5Ac.3677T>C (p.Ile1226Thr)
c.3680T>C (p.Ile1227Thr)
c.3518T>C (p.Ile1173Thr)
c.3551T>C (p.Ile1184Thr)
3g.38566569A>TCA352149463SCN5Ac.3677T>A (p.Ile1226Asn)
c.3680T>A (p.Ile1227Asn)
c.3518T>A (p.Ile1173Asn)
c.3551T>A (p.Ile1184Asn)
3g.38566570T>ACA352149464SCN5Ac.3676A>T (p.Ile1226Phe)
c.3679A>T (p.Ile1227Phe)
c.3517A>T (p.Ile1173Phe)
c.3550A>T (p.Ile1184Phe)
3g.38566570T>CCA352149468SCN5Ac.3676A>G (p.Ile1226Val)
c.3679A>G (p.Ile1227Val)
c.3517A>G (p.Ile1173Val)
c.3550A>G (p.Ile1184Val)
3g.38566570T>GCA352149466SCN5Ac.3676A>C (p.Ile1226Leu)
c.3679A>C (p.Ile1227Leu)
c.3517A>C (p.Ile1173Leu)
c.3550A>C (p.Ile1184Leu)
3g.38566571G>ACA433136968SCN5Ac.3675C>T (p.Asp1225=)
c.3678C>T (p.Asp1226=)
c.3516C>T (p.Asp1172=)
c.3549C>T (p.Asp1183=)
 dbSNP
3g.38566571G>CCA352149470SCN5Ac.3675C>G (p.Asp1225Glu)
c.3678C>G (p.Asp1226Glu)
c.3516C>G (p.Asp1172Glu)
c.3549C>G (p.Asp1183Glu)
3g.38566571G=CA1358569832SCN5Ac.3675C= (p.Asp1225=)
c.3678C= (p.Asp1226=)
c.3516C= (p.Asp1172=)
c.3549C= (p.Asp1183=)
3g.38566571G>TCA352149471SCN5Ac.3675C>A (p.Asp1225Glu)
c.3678C>A (p.Asp1226Glu)
c.3516C>A (p.Asp1172Glu)
c.3549C>A (p.Asp1183Glu)
3g.38566572T>ACA352149474SCN5Ac.3674A>T (p.Asp1225Val)
c.3677A>T (p.Asp1226Val)
c.3515A>T (p.Asp1172Val)
c.3548A>T (p.Asp1183Val)
3g.38566572T>CCA352149476SCN5Ac.3674A>G (p.Asp1225Gly)
c.3677A>G (p.Asp1226Gly)
c.3515A>G (p.Asp1172Gly)
c.3548A>G (p.Asp1183Gly)
3g.38566572T>GCA352149480SCN5Ac.3674A>C (p.Asp1225Ala)
c.3677A>C (p.Asp1226Ala)
c.3515A>C (p.Asp1172Ala)
c.3548A>C (p.Asp1183Ala)
3g.38566573C>ACA352149482SCN5Ac.3673G>T (p.Asp1225Tyr)
c.3676G>T (p.Asp1226Tyr)
c.3514G>T (p.Asp1172Tyr)
c.3547G>T (p.Asp1183Tyr)
3g.38566573C>GCA352149484SCN5Ac.3673G>C (p.Asp1225His)
c.3676G>C (p.Asp1226His)
c.3514G>C (p.Asp1172His)
c.3547G>C (p.Asp1183His)
3g.38566573C>TCA352149487SCN5Ac.3673G>A (p.Asp1225Asn)
c.3676G>A (p.Asp1226Asn)
c.3514G>A (p.Asp1172Asn)
c.3547G>A (p.Asp1183Asn)
3g.38566574C>ACA352149489SCN5Ac.3672G>T (p.Glu1224Asp)
c.3675G>T (p.Glu1225Asp)
c.3513G>T (p.Glu1171Asp)
c.3546G>T (p.Glu1182Asp)
3g.38566574C>GCA352149490SCN5Ac.3672G>C (p.Glu1224Asp)
c.3675G>C (p.Glu1225Asp)
c.3513G>C (p.Glu1171Asp)
c.3546G>C (p.Glu1182Asp)
3g.38566574C>TCA433136979SCN5Ac.3672G>A (p.Glu1224=)
c.3675G>A (p.Glu1225=)
c.3513G>A (p.Glu1171=)
c.3546G>A (p.Glu1182=)
 ClinVar COSMIC COSMIC COSMIC
3g.38566575T>ACA352149507SCN5Ac.3671A>T (p.Glu1224Val)
c.3674A>T (p.Glu1225Val)
c.3512A>T (p.Glu1171Val)
c.3545A>T (p.Glu1182Val)
3g.38566575T>CCA352149505SCN5Ac.3671A>G (p.Glu1224Gly)
c.3674A>G (p.Glu1225Gly)
c.3512A>G (p.Glu1171Gly)
c.3545A>G (p.Glu1182Gly)
3g.38566575T>GCA352149493SCN5Ac.3671A>C (p.Glu1224Ala)
c.3674A>C (p.Glu1225Ala)
c.3512A>C (p.Glu1171Ala)
c.3545A>C (p.Glu1182Ala)
3g.38566576C>ACA352149510SCN5Ac.3670G>T (p.Glu1224Ter)
c.3673G>T (p.Glu1225Ter)
c.3511G>T (p.Glu1171Ter)
c.3544G>T (p.Glu1182Ter)
 dbSNP
3g.38566576C=CA1358569838SCN5Ac.3670G= (p.Glu1224=)
c.3673G= (p.Glu1225=)
c.3511G= (p.Glu1171=)
c.3544G= (p.Glu1182=)
3g.38566576C>GCA352149513SCN5Ac.3670G>C (p.Glu1224Gln)
c.3673G>C (p.Glu1225Gln)
c.3511G>C (p.Glu1171Gln)
c.3544G>C (p.Glu1182Gln)
 ClinVar
3g.38566576C>TCA017399SCN5Ac.3670G>A (p.Glu1224Lys)
c.3673G>A (p.Glu1225Lys)
c.3511G>A (p.Glu1171Lys)
c.3544G>A (p.Glu1182Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
3g.38566577G>ACA433136988SCN5Ac.3669C>T (p.Phe1223=)
c.3672C>T (p.Phe1224=)
c.3510C>T (p.Phe1170=)
c.3543C>T (p.Phe1181=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38566577G>CCA352149516SCN5Ac.3669C>G (p.Phe1223Leu)
c.3672C>G (p.Phe1224Leu)
c.3510C>G (p.Phe1170Leu)
c.3543C>G (p.Phe1181Leu)
3g.38566577G=CA1358569845SCN5Ac.3669C= (p.Phe1223=)
c.3672C= (p.Phe1224=)
c.3510C= (p.Phe1170=)
c.3543C= (p.Phe1181=)
3g.38566577G>TCA352149530SCN5Ac.3669C>A (p.Phe1223Leu)
c.3672C>A (p.Phe1224Leu)
c.3510C>A (p.Phe1170Leu)
c.3543C>A (p.Phe1181Leu)
3g.38566578A>CCA352149540SCN5Ac.3668T>G (p.Phe1223Cys)
c.3671T>G (p.Phe1224Cys)
c.3509T>G (p.Phe1170Cys)
c.3542T>G (p.Phe1181Cys)
3g.38566578A>GCA352149544SCN5Ac.3668T>C (p.Phe1223Ser)
c.3671T>C (p.Phe1224Ser)
c.3509T>C (p.Phe1170Ser)
c.3542T>C (p.Phe1181Ser)
3g.38566578A>TCA352149542SCN5Ac.3668T>A (p.Phe1223Tyr)
c.3671T>A (p.Phe1224Tyr)
c.3509T>A (p.Phe1170Tyr)
c.3542T>A (p.Phe1181Tyr)
3g.38566579A>CCA352149552SCN5Ac.3667T>G (p.Phe1223Val)
c.3670T>G (p.Phe1224Val)
c.3508T>G (p.Phe1170Val)
c.3541T>G (p.Phe1181Val)
3g.38566579A>GCA352149555SCN5Ac.3667T>C (p.Phe1223Leu)
c.3670T>C (p.Phe1224Leu)
c.3508T>C (p.Phe1170Leu)
c.3541T>C (p.Phe1181Leu)
3g.38566579A>TCA352149558SCN5Ac.3667T>A (p.Phe1223Ile)
c.3670T>A (p.Phe1224Ile)
c.3508T>A (p.Phe1170Ile)
c.3541T>A (p.Phe1181Ile)
3g.38566580G>ACA72947623SCN5Ac.3666C>T (p.Ala1222=)
c.3669C>T (p.Ala1223=)
c.3507C>T (p.Ala1169=)
c.3540C>T (p.Ala1180=)
 dbSNP
3g.38566580G>CCA433136995SCN5Ac.3666C>G (p.Ala1222=)
c.3669C>G (p.Ala1223=)
c.3507C>G (p.Ala1169=)
c.3540C>G (p.Ala1180=)
3g.38566580G=CA1358569847SCN5Ac.3666C= (p.Ala1222=)
c.3669C= (p.Ala1223=)
c.3507C= (p.Ala1169=)
c.3540C= (p.Ala1180=)
3g.38566580G>TCA433136996SCN5Ac.3666C>A (p.Ala1222=)
c.3669C>A (p.Ala1223=)
c.3507C>A (p.Ala1169=)
c.3540C>A (p.Ala1180=)
3g.38566581G>ACA352149576SCN5Ac.3665C>T (p.Ala1222Val)
c.3668C>T (p.Ala1223Val)
c.3506C>T (p.Ala1169Val)
c.3539C>T (p.Ala1180Val)
3g.38566581G>CCA352149578SCN5Ac.3665C>G (p.Ala1222Gly)
c.3668C>G (p.Ala1223Gly)
c.3506C>G (p.Ala1169Gly)
c.3539C>G (p.Ala1180Gly)
3g.38566581G>TCA352149583SCN5Ac.3665C>A (p.Ala1222Asp)
c.3668C>A (p.Ala1223Asp)
c.3506C>A (p.Ala1169Asp)
c.3539C>A (p.Ala1180Asp)
3g.38566582C>ACA352149585SCN5Ac.3664G>T (p.Ala1222Ser)
c.3667G>T (p.Ala1223Ser)
c.3505G>T (p.Ala1169Ser)
c.3538G>T (p.Ala1180Ser)
3g.38566582C=CA1358569854SCN5Ac.3664G= (p.Ala1222=)
c.3667G= (p.Ala1223=)
c.3505G= (p.Ala1169=)
c.3538G= (p.Ala1180=)
3g.38566582C>GCA339598SCN5Ac.3664G>C (p.Ala1222Pro)
c.3667G>C (p.Ala1223Pro)
c.3505G>C (p.Ala1169Pro)
c.3538G>C (p.Ala1180Pro)
 ClinVar dbSNP
3g.38566582C>TCA352149589SCN5Ac.3664G>A (p.Ala1222Thr)
c.3667G>A (p.Ala1223Thr)
c.3505G>A (p.Ala1169Thr)
c.3538G>A (p.Ala1180Thr)
3g.38566583delCA2586972092SCN5Ac.3664del
c.3667del
c.3505del
c.3538del
3g.38566583C>ACA352149594SCN5Ac.3664-1G>T (n.3664-1G>T)
c.3667-1G>T (n.3667-1G>T)
c.3505-1G>T (n.3505-1G>T)
c.3538-1G>T (n.3538-1G>T)
3g.38566583C>GCA352149597SCN5Ac.3664-1G>C (n.3664-1G>C)
c.3667-1G>C (n.3667-1G>C)
c.3505-1G>C (n.3505-1G>C)
c.3538-1G>C (n.3538-1G>C)
3g.38566583C>TCA352149599SCN5Ac.3664-1G>A (n.3664-1G>A)
c.3667-1G>A (n.3667-1G>A)
c.3505-1G>A (n.3505-1G>A)
c.3538-1G>A (n.3538-1G>A)
3g.38566584T>ACA352149602SCN5Ac.3664-2A>T (n.3664-2A>T)
c.3667-2A>T (n.3667-2A>T)
c.3505-2A>T (n.3505-2A>T)
c.3538-2A>T (n.3538-2A>T)
 dbSNP
3g.38566584T>CCA352149607SCN5Ac.3664-2A>G (n.3664-2A>G)
c.3667-2A>G (n.3667-2A>G)
c.3505-2A>G (n.3505-2A>G)
c.3538-2A>G (n.3538-2A>G)
3g.38566584T>GCA352149604SCN5Ac.3664-2A>C (n.3664-2A>C)
c.3667-2A>C (n.3667-2A>C)
c.3505-2A>C (n.3505-2A>C)
c.3538-2A>C (n.3538-2A>C)
3g.38566584T=CA1358569858SCN5Ac.3664-2A= (n.3664-2A=)
c.3667-2A= (n.3667-2A=)
c.3505-2A= (n.3505-2A=)
c.3538-2A= (n.3538-2A=)
3g.38566585G>ACA2665111943SCN5Ac.3664-3C>T (n.3664-3C>T)
c.3667-3C>T (n.3667-3C>T)
c.3505-3C>T (n.3505-3C>T)
c.3538-3C>T (n.3538-3C>T)
 gnomAD v4
3g.38566585_38566595delinsGCAGACAAGGCCA1358569860SCN5Ac.3664-13_3664-3delinsGCCTTGTCTGC (n.3664-13_3664-3delinsGCCTTGTCTGC)
c.3667-13_3667-3delinsGCCTTGTCTGC (n.3667-13_3667-3delinsGCCTTGTCTGC)
c.3505-13_3505-3delinsGCCTTGTCTGC (n.3505-13_3505-3delinsGCCTTGTCTGC)
c.3538-13_3538-3delinsGCCTTGTCTGC (n.3538-13_3538-3delinsGCCTTGTCTGC)
3g.38566586C>ACA2665111944SCN5Ac.3664-4G>T (n.3664-4G>T)
c.3667-4G>T (n.3667-4G>T)
c.3505-4G>T (n.3505-4G>T)
c.3538-4G>T (n.3538-4G>T)
 gnomAD v4
3g.38566586C=CA1358569862SCN5Ac.3664-4G= (n.3664-4G=)
c.3667-4G= (n.3667-4G=)
c.3505-4G= (n.3505-4G=)
c.3538-4G= (n.3538-4G=)
3g.38566586C>TCA062176SCN5Ac.3664-4G>A (n.3664-4G>A)
c.3667-4G>A (n.3667-4G>A)
c.3505-4G>A (n.3505-4G>A)
c.3538-4G>A (n.3538-4G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38566595_38566604delCA1358569861SCN5Ac.3664-13_3664-4del (n.3664-13_3664-4del)
c.3667-13_3667-4del (n.3667-13_3667-4del)
c.3505-13_3505-4del (n.3505-13_3505-4del)
c.3538-13_3538-4del (n.3538-13_3538-4del)
 dbSNP gnomAD v4
3g.38566587A>GCA2665111945SCN5Ac.3664-5T>C (n.3664-5T>C)
c.3667-5T>C (n.3667-5T>C)
c.3505-5T>C (n.3505-5T>C)
c.3538-5T>C (n.3538-5T>C)
 gnomAD v4
3g.38566588G>ACA1358569865SCN5Ac.3664-6C>T (n.3664-6C>T)
c.3667-6C>T (n.3667-6C>T)
c.3505-6C>T (n.3505-6C>T)
c.3538-6C>T (n.3538-6C>T)
 dbSNP
3g.38566588G=CA1358569864SCN5Ac.3664-6C= (n.3664-6C=)
c.3667-6C= (n.3667-6C=)
c.3505-6C= (n.3505-6C=)
c.3538-6C= (n.3538-6C=)
3g.38566589A=CA1358569869SCN5Ac.3664-7T= (n.3664-7T=)
c.3667-7T= (n.3667-7T=)
c.3505-7T= (n.3505-7T=)
c.3538-7T= (n.3538-7T=)
3g.38566589A>TCA017393SCN5Ac.3664-7T>A (n.3664-7T>A)
c.3667-7T>A (n.3667-7T>A)
c.3505-7T>A (n.3505-7T>A)
c.3538-7T>A (n.3538-7T>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38566591A=CA1358569873SCN5Ac.3664-9T= (n.3664-9T=)
c.3667-9T= (n.3667-9T=)
c.3505-9T= (n.3505-9T=)
c.3538-9T= (n.3538-9T=)
3g.38566591A>CCA2825001221SCN5Ac.3664-9T>G (n.3664-9T>G)
c.3667-9T>G (n.3667-9T>G)
c.3505-9T>G (n.3505-9T>G)
c.3538-9T>G (n.3538-9T>G)
 ClinVar
3g.38566591A>GCA062183SCN5Ac.3664-9T>C (n.3664-9T>C)
c.3667-9T>C (n.3667-9T>C)
c.3505-9T>C (n.3505-9T>C)
c.3538-9T>C (n.3538-9T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38566592A=CA1358569878SCN5Ac.3664-10T= (n.3664-10T=)
c.3667-10T= (n.3667-10T=)
c.3505-10T= (n.3505-10T=)
c.3538-10T= (n.3538-10T=)
3g.38566592A>TCA542615573SCN5Ac.3664-10T>A (n.3664-10T>A)
c.3667-10T>A (n.3667-10T>A)
c.3505-10T>A (n.3505-10T>A)
c.3538-10T>A (n.3538-10T>A)
 dbSNP gnomAD v2 gnomAD v4
3g.38566594G>ACA2577553240SCN5Ac.3664-12C>T (n.3664-12C>T)
c.3667-12C>T (n.3667-12C>T)
c.3505-12C>T (n.3505-12C>T)
c.3538-12C>T (n.3538-12C>T)
3g.38566594G>CCA2577553241SCN5Ac.3664-12C>G (n.3664-12C>G)
c.3667-12C>G (n.3667-12C>G)
c.3505-12C>G (n.3505-12C>G)
c.3538-12C>G (n.3538-12C>G)
 ClinVar gnomAD v4
3g.38566594G>TCA2499216746SCN5Ac.3664-12C>A (n.3664-12C>A)
c.3667-12C>A (n.3667-12C>A)
c.3505-12C>A (n.3505-12C>A)
c.3538-12C>A (n.3538-12C>A)
 ClinVar dbSNP gnomAD v4
3g.38566595C>ACA1358569881SCN5Ac.3664-13G>T (n.3664-13G>T)
c.3667-13G>T (n.3667-13G>T)
c.3505-13G>T (n.3505-13G>T)
c.3538-13G>T (n.3538-13G>T)
 dbSNP
3g.38566595C=CA1358569880SCN5Ac.3664-13G= (n.3664-13G=)
c.3667-13G= (n.3667-13G=)
c.3505-13G= (n.3505-13G=)
c.3538-13G= (n.3538-13G=)
3g.38566596C>GCA2665111946SCN5Ac.3664-14G>C (n.3664-14G>C)
c.3667-14G>C (n.3667-14G>C)
c.3505-14G>C (n.3505-14G>C)
c.3538-14G>C (n.3538-14G>C)
 gnomAD v4
3g.38566597A=CA1358569883SCN5Ac.3664-15T= (n.3664-15T=)
c.3667-15T= (n.3667-15T=)
c.3505-15T= (n.3505-15T=)
c.3538-15T= (n.3538-15T=)
3g.38566597A>GCA1046996772SCN5Ac.3664-15T>C (n.3664-15T>C)
c.3667-15T>C (n.3667-15T>C)
c.3505-15T>C (n.3505-15T>C)
c.3538-15T>C (n.3538-15T>C)
 dbSNP gnomAD v3 gnomAD v4
3g.38566598G>ACA1358569885SCN5Ac.3664-16C>T (n.3664-16C>T)
c.3667-16C>T (n.3667-16C>T)
c.3505-16C>T (n.3505-16C>T)
c.3538-16C>T (n.3538-16C>T)
 ClinVar dbSNP gnomAD v4
3g.38566598G=CA1358569886SCN5Ac.3664-16C= (n.3664-16C=)
c.3667-16C= (n.3667-16C=)
c.3505-16C= (n.3505-16C=)
c.3538-16C= (n.3538-16C=)
3g.38566599A>GCA2577553242SCN5Ac.3664-17T>C (n.3664-17T>C)
c.3667-17T>C (n.3667-17T>C)
c.3505-17T>C (n.3505-17T>C)
c.3538-17T>C (n.3538-17T>C)
3g.38566600C>ACA2665111947SCN5Ac.3664-18G>T (n.3664-18G>T)
c.3667-18G>T (n.3667-18G>T)
c.3505-18G>T (n.3505-18G>T)
c.3538-18G>T (n.3538-18G>T)
 gnomAD v4
3g.38566600C=CA1358569887SCN5Ac.3664-18G= (n.3664-18G=)
c.3667-18G= (n.3667-18G=)
c.3505-18G= (n.3505-18G=)
c.3538-18G= (n.3538-18G=)
3g.38566600C>GCA1046996776SCN5Ac.3664-18G>C (n.3664-18G>C)
c.3667-18G>C (n.3667-18G>C)
c.3505-18G>C (n.3505-18G>C)
c.3538-18G>C (n.3538-18G>C)
 ClinVar dbSNP
3g.38566600C>TCA2665111948SCN5Ac.3664-18G>A (n.3664-18G>A)
c.3667-18G>A (n.3667-18G>A)
c.3505-18G>A (n.3505-18G>A)
c.3538-18G>A (n.3538-18G>A)
 gnomAD v4
3g.38566603G>ACA062156SCN5Ac.3664-21C>T (n.3664-21C>T)
c.3667-21C>T (n.3667-21C>T)
c.3505-21C>T (n.3505-21C>T)
c.3538-21C>T (n.3538-21C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38566603G=CA1358569888SCN5Ac.3664-21C= (n.3664-21C=)
c.3667-21C= (n.3667-21C=)
c.3505-21C= (n.3505-21C=)
c.3538-21C= (n.3538-21C=)
3g.38566604G>TCA2665111949SCN5Ac.3664-22C>A (n.3664-22C>A)
c.3667-22C>A (n.3667-22C>A)
c.3505-22C>A (n.3505-22C>A)
c.3538-22C>A (n.3538-22C>A)
 gnomAD v4
3g.38566605T>GCA1358569890SCN5Ac.3664-23A>C (n.3664-23A>C)
c.3667-23A>C (n.3667-23A>C)
c.3505-23A>C (n.3505-23A>C)
c.3538-23A>C (n.3538-23A>C)
 dbSNP
3g.38566605T=CA1358569889SCN5Ac.3664-23A= (n.3664-23A=)
c.3667-23A= (n.3667-23A=)
c.3505-23A= (n.3505-23A=)
c.3538-23A= (n.3538-23A=)
3g.38566611T>CCA2665111950SCN5Ac.3664-29A>G (n.3664-29A>G)
c.3667-29A>G (n.3667-29A>G)
c.3505-29A>G (n.3505-29A>G)
c.3538-29A>G (n.3538-29A>G)
 gnomAD v4
3g.38566611T>GCA062160SCN5Ac.3664-29A>C (n.3664-29A>C)
c.3667-29A>C (n.3667-29A>C)
c.3505-29A>C (n.3505-29A>C)
c.3538-29A>C (n.3538-29A>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.38566611T=CA1358569891SCN5Ac.3664-29A= (n.3664-29A=)
c.3667-29A= (n.3667-29A=)
c.3505-29A= (n.3505-29A=)
c.3538-29A= (n.3538-29A=)
3g.38566616C=CA1358569894SCN5Ac.3664-34G= (n.3664-34G=)
c.3667-34G= (n.3667-34G=)
c.3505-34G= (n.3505-34G=)
c.3538-34G= (n.3538-34G=)
3g.38566616C>TCA1046996796SCN5Ac.3664-34G>A (n.3664-34G>A)
c.3667-34G>A (n.3667-34G>A)
c.3505-34G>A (n.3505-34G>A)
c.3538-34G>A (n.3538-34G>A)
 dbSNP gnomAD v3 gnomAD v4
3g.38566617delCA2665111951SCN5Ac.3664-34del (n.3664-34del)
c.3667-34del (n.3667-34del)
c.3505-34del (n.3505-34del)
c.3538-34del (n.3538-34del)
 gnomAD v4
3g.38566617C>TCA2755899979SCN5Ac.3664-35G>A (n.3664-35G>A)
c.3667-35G>A (n.3667-35G>A)
c.3505-35G>A (n.3505-35G>A)
c.3538-35G>A (n.3538-35G>A)
3g.38566619G>ACA2665111952SCN5Ac.3664-37C>T (n.3664-37C>T)
c.3667-37C>T (n.3667-37C>T)
c.3505-37C>T (n.3505-37C>T)
c.3538-37C>T (n.3538-37C>T)
 gnomAD v4
3g.38566620G>ACA062161SCN5Ac.3664-38C>T (n.3664-38C>T)
c.3667-38C>T (n.3667-38C>T)
c.3505-38C>T (n.3505-38C>T)
c.3538-38C>T (n.3538-38C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38566620G=CA1358569896SCN5Ac.3664-38C= (n.3664-38C=)
c.3667-38C= (n.3667-38C=)
c.3505-38C= (n.3505-38C=)
c.3538-38C= (n.3538-38C=)
3g.38566620G>TCA2665111953SCN5Ac.3664-38C>A (n.3664-38C>A)
c.3667-38C>A (n.3667-38C>A)
c.3505-38C>A (n.3505-38C>A)
c.3538-38C>A (n.3538-38C>A)
 gnomAD v4
3g.38566621A=CA1358569897SCN5Ac.3664-39T= (n.3664-39T=)
c.3667-39T= (n.3667-39T=)
c.3505-39T= (n.3505-39T=)
c.3538-39T= (n.3538-39T=)
3g.38566621A>CCA1358569898SCN5Ac.3664-39T>G (n.3664-39T>G)
c.3667-39T>G (n.3667-39T>G)
c.3505-39T>G (n.3505-39T>G)
c.3538-39T>G (n.3538-39T>G)
 dbSNP
3g.38566622C=CA1358569900SCN5Ac.3664-40G= (n.3664-40G=)
c.3667-40G= (n.3667-40G=)
c.3505-40G= (n.3505-40G=)
c.3538-40G= (n.3538-40G=)
3g.38566622C>TCA062165SCN5Ac.3664-40G>A (n.3664-40G>A)
c.3667-40G>A (n.3667-40G>A)
c.3505-40G>A (n.3505-40G>A)
c.3538-40G>A (n.3538-40G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched