Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38603907C>ACA352146662SCN5Ac.1695G>T (p.Trp565Cys)
c.1566G>T (p.Trp522Cys)
3g.38603907C=CA1358584961SCN5Ac.1695G= (p.Trp565=)
c.1566G= (p.Trp522=)
3g.38603907C>GCA352146667SCN5Ac.1695G>C (p.Trp565Cys)
c.1566G>C (p.Trp522Cys)
3g.38603907C>TCA352146669SCN5Ac.1695G>A (p.Trp565Ter)
c.1566G>A (p.Trp522Ter)
dbSNP
3g.38603908C>ACA352146671SCN5Ac.1694G>T (p.Trp565Leu)
c.1565G>T (p.Trp522Leu)
3g.38603908C>GCA352146673SCN5Ac.1694G>C (p.Trp565Ser)
c.1565G>C (p.Trp522Ser)
3g.38603908C>TCA352146675SCN5Ac.1694G>A (p.Trp565Ter)
c.1565G>A (p.Trp522Ter)
3g.38603909A=CA1358584962SCN5Ac.1693T= (p.Trp565=)
c.1564T= (p.Trp522=)
3g.38603909A>CCA352146682SCN5Ac.1693T>G (p.Trp565Gly)
c.1564T>G (p.Trp522Gly)
3g.38603909A>GCA352146678SCN5Ac.1693T>C (p.Trp565Arg)
c.1564T>C (p.Trp522Arg)
dbSNP
3g.38603909A>TCA352146680SCN5Ac.1693T>A (p.Trp565Arg)
c.1564T>A (p.Trp522Arg)
3g.38603910G>ACA433332962SCN5Ac.1692C>T (p.Pro564=)
c.1563C>T (p.Pro521=)
3g.38603910G>CCA433332964SCN5Ac.1692C>G (p.Pro564=)
c.1563C>G (p.Pro521=)
3g.38603910G>TCA433332967SCN5Ac.1692C>A (p.Pro564=)
c.1563C>A (p.Pro521=)
3g.38603911G>ACA352146684SCN5Ac.1691C>T (p.Pro564Leu)
c.1562C>T (p.Pro521Leu)
3g.38603911G>CCA352146686SCN5Ac.1691C>G (p.Pro564Arg)
c.1562C>G (p.Pro521Arg)
3g.38603911G>TCA352146689SCN5Ac.1691C>A (p.Pro564His)
c.1562C>A (p.Pro521His)
3g.38603912G>ACA352146692SCN5Ac.1690C>T (p.Pro564Ser)
c.1561C>T (p.Pro521Ser)
ClinVar dbSNP
3g.38603912G>CCA352146703SCN5Ac.1690C>G (p.Pro564Ala)
c.1561C>G (p.Pro521Ala)
3g.38603912G=CA1358584963SCN5Ac.1690C= (p.Pro564=)
c.1561C= (p.Pro521=)
3g.38603912G>TCA352146706SCN5Ac.1690C>A (p.Pro564Thr)
c.1561C>A (p.Pro521Thr)
3g.38603913C>ACA433332971SCN5Ac.1689G>T (p.Val563=)
c.1560G>T (p.Val520=)
3g.38603913C>GCA433332972SCN5Ac.1689G>C (p.Val563=)
c.1560G>C (p.Val520=)
3g.38603913C>TCA433332973SCN5Ac.1689G>A (p.Val563=)
c.1560G>A (p.Val520=)
gnomAD v4
3g.38603914A=CA1358584964SCN5Ac.1688T= (p.Val563=)
c.1559T= (p.Val520=)
3g.38603914A>CCA352146709SCN5Ac.1688T>G (p.Val563Gly)
c.1559T>G (p.Val520Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38603914A>GCA352146712SCN5Ac.1688T>C (p.Val563Ala)
c.1559T>C (p.Val520Ala)
3g.38603914A>TCA352146714SCN5Ac.1688T>A (p.Val563Glu)
c.1559T>A (p.Val520Glu)
3g.38603915C>ACA352146717SCN5Ac.1687G>T (p.Val563Leu)
c.1558G>T (p.Val520Leu)
ClinVar dbSNP gnomAD v4
3g.38603915C>GCA352146720SCN5Ac.1687G>C (p.Val563Leu)
c.1558G>C (p.Val520Leu)
gnomAD v4
3g.38603915C>TCA352146722SCN5Ac.1687G>A (p.Val563Met)
c.1558G>A (p.Val520Met)
3g.38603916C>ACA433332986SCN5Ac.1686G>T (p.Leu562=)
c.1557G>T (p.Leu519=)
3g.38603916C>GCA433332988SCN5Ac.1686G>C (p.Leu562=)
c.1557G>C (p.Leu519=)
3g.38603916C>TCA433332992SCN5Ac.1686G>A (p.Leu562=)
c.1557G>A (p.Leu519=)
3g.38603917A>CCA352146727SCN5Ac.1685T>G (p.Leu562Arg)
c.1556T>G (p.Leu519Arg)
3g.38603917A>GCA352146731SCN5Ac.1685T>C (p.Leu562Pro)
c.1556T>C (p.Leu519Pro)
gnomAD v4
3g.38603917A>TCA352146729SCN5Ac.1685T>A (p.Leu562Gln)
c.1556T>A (p.Leu519Gln)
3g.38603918G>ACA433333007SCN5Ac.1684C>T (p.Leu562=)
c.1555C>T (p.Leu519=)
dbSNP gnomAD v2
3g.38603918G>CCA352146734SCN5Ac.1684C>G (p.Leu562Val)
c.1555C>G (p.Leu519Val)
3g.38603918G=CA1358584965SCN5Ac.1684C= (p.Leu562=)
c.1555C= (p.Leu519=)
3g.38603918G>TCA352146737SCN5Ac.1684C>A (p.Leu562Met)
c.1555C>A (p.Leu519Met)
3g.38603919C>ACA433333010SCN5Ac.1683G>T (p.Leu561=)
c.1554G>T (p.Leu518=)
3g.38603919C=CA1358584966SCN5Ac.1683G= (p.Leu561=)
c.1554G= (p.Leu518=)
3g.38603919C>GCA433333013SCN5Ac.1683G>C (p.Leu561=)
c.1554G>C (p.Leu518=)
3g.38603919C>TCA433333012SCN5Ac.1683G>A (p.Leu561=)
c.1554G>A (p.Leu518=)
dbSNP gnomAD v2 gnomAD v4
3g.38603920A>CCA352146740SCN5Ac.1682T>G (p.Leu561Arg)
c.1553T>G (p.Leu518Arg)
3g.38603920A>GCA352146742SCN5Ac.1682T>C (p.Leu561Pro)
c.1553T>C (p.Leu518Pro)
3g.38603920A>TCA352146745SCN5Ac.1682T>A (p.Leu561Gln)
c.1553T>A (p.Leu518Gln)
3g.38603921G>ACA015163SCN5Ac.1681C>T (p.Leu561=)
c.1552C>T (p.Leu518=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38603921G>CCA352146750SCN5Ac.1681C>G (p.Leu561Val)
c.1552C>G (p.Leu518Val)

Number of alleles fetched