Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
3g.38603927T>CCA352146782SCN5Ac.1675A>G (p.Thr559Ala)
c.1546A>G (p.Thr516Ala)
3g.38603927T>GCA352146784SCN5Ac.1675A>C (p.Thr559Pro)
c.1546A>C (p.Thr516Pro)
dbSNP
3g.38603927T=CA1358584970SCN5Ac.1675A= (p.Thr559=)
c.1546A= (p.Thr516=)
3g.38603928G>ACA433333049SCN5Ac.1674C>T (p.His558=)
c.1545C>T (p.His515=)
3g.38603928G>CCA352146786SCN5Ac.1674C>G (p.His558Gln)
c.1545C>G (p.His515Gln)
ClinVar dbSNP
3g.38603928G=CA1358584971SCN5Ac.1674C= (p.His558=)
c.1545C= (p.His515=)
3g.38603928G>TCA352146788SCN5Ac.1674C>A (p.His558Gln)
c.1545C>A (p.His515Gln)
3g.38603929T>ACA352146790SCN5Ac.1673A>T (p.His558Leu)
c.1544A>T (p.His515Leu)
3g.38603929T>CCA015145SCN5Ac.1673A>G (p.His558Arg)
c.1544A>G (p.His515Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.[38603929T>C;38604067G>A]CA085349SCN5Ac.[1535C>T;1673A>G] (p.[Thr512Ile;His558Arg])
c.[1406C>T;1544A>G] (p.[Thr469Ile;His515Arg])
3g.38603929T>GCA352146796SCN5Ac.1673A>C (p.His558Pro)
c.1544A>C (p.His515Pro)
3g.38603929T=CA1358584972SCN5Ac.1673A= (p.His558=)
c.1544A= (p.His515=)
3g.38603929_38603930delinsCACA1139655765SCN5Ac.1672_1673delinsTG (p.His558Cys)
c.1543_1544delinsTG (p.His515Cys)
ClinVar
3g.38603930G>ACA72939207SCN5Ac.1672C>T (p.His558Tyr)
c.1543C>T (p.His515Tyr)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38603930G>CCA352146802SCN5Ac.1672C>G (p.His558Asp)
c.1543C>G (p.His515Asp)
3g.38603930G=CA1358584973SCN5Ac.1672C= (p.His558=)
c.1543C= (p.His515=)
3g.38603930G>TCA352146799SCN5Ac.1672C>A (p.His558Asn)
c.1543C>A (p.His515Asn)
3g.38603931delCA2586971911SCN5Ac.1672del (p.His558ThrfsTer?)
c.1543del (p.His515ThrfsTer?)
gnomAD v4
3g.38603931G>ACA433333057SCN5Ac.1671C>T (p.His557=)
c.1542C>T (p.His514=)
gnomAD v4
3g.38603931G>CCA058476SCN5Ac.1671C>G (p.His557Gln)
c.1542C>G (p.His514Gln)
ClinVar dbSNP ExAC gnomAD v2
3g.38603931G=CA1358584974SCN5Ac.1671C= (p.His557=)
c.1542C= (p.His514=)

Number of alleles fetched