Chr Mutation (hg38) CAid Gene Transcript Linkouts
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=)

Number of alleles fetched