Chr Mutation (hg38) CAid Gene Transcript Linkouts
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.38603916dupCA2990484004SCN5Ac.1687dup (p.Val563GlyfsTer?)
c.1558dup (p.Val520GlyfsTer?)
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)
3g.38603921G=CA1358584967SCN5Ac.1681C= (p.Leu561=)
c.1552C= (p.Leu518=)
3g.38603921G>TCA352146752SCN5Ac.1681C>A (p.Leu561Met)
c.1552C>A (p.Leu518Met)
3g.38603922T>ACA433333024SCN5Ac.1680A>T (p.Ser560=)
c.1551A>T (p.Ser517=)
3g.38603922T>CCA433333021SCN5Ac.1680A>G (p.Ser560=)
c.1551A>G (p.Ser517=)
3g.38603922T>GCA433333020SCN5Ac.1680A>C (p.Ser560=)
c.1551A>C (p.Ser517=)
3g.38603923G>ACA352146756SCN5Ac.1679C>T (p.Ser560Leu)
c.1550C>T (p.Ser517Leu)
ClinVar
3g.38603923G>CCA352146759SCN5Ac.1679C>G (p.Ser560Ter)
c.1550C>G (p.Ser517Ter)
ClinVar
3g.38603923G>TCA352146762SCN5Ac.1679C>A (p.Ser560Ter)
c.1550C>A (p.Ser517Ter)
3g.38603924A>CCA352146769SCN5Ac.1678T>G (p.Ser560Ala)
c.1549T>G (p.Ser517Ala)
3g.38603924A>GCA352146766SCN5Ac.1678T>C (p.Ser560Pro)
c.1549T>C (p.Ser517Pro)
3g.38603924A>TCA352146765SCN5Ac.1678T>A (p.Ser560Thr)
c.1549T>A (p.Ser517Thr)
3g.38603925T>ACA433333037SCN5Ac.1677A>T (p.Thr559=)
c.1548A>T (p.Thr516=)
3g.38603925T>CCA72939197SCN5Ac.1677A>G (p.Thr559=)
c.1548A>G (p.Thr516=)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38603925T>GCA433333038SCN5Ac.1677A>C (p.Thr559=)
c.1548A>C (p.Thr516=)
3g.38603925T=CA1358584968SCN5Ac.1677A= (p.Thr559=)
c.1548A= (p.Thr516=)
3g.38603926G>ACA015154SCN5Ac.1676C>T (p.Thr559Ile)
c.1547C>T (p.Thr516Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38603926G>CCA058488SCN5Ac.1676C>G (p.Thr559Arg)
c.1547C>G (p.Thr516Arg)
dbSNP ExAC gnomAD v4
3g.38603926G=CA1358584969SCN5Ac.1676C= (p.Thr559=)
c.1547C= (p.Thr516=)
3g.38603926G>TCA352146777SCN5Ac.1676C>A (p.Thr559Lys)
c.1547C>A (p.Thr516Lys)
ClinVar dbSNP
3g.38603927T>ACA352146781SCN5Ac.1675A>T (p.Thr559Ser)
c.1546A>T (p.Thr516Ser)

Number of alleles fetched