Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38605980_38605987delCA2580069739SCN5Ac.1305_1312del (p.Gln435HisfsTer22)
c.1176_1183del (p.Gln392HisfsTer22)
ClinVar
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=)

Number of alleles fetched