Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38603812C>ACA352146152SCN5Ac.1790G>T (p.Cys597Phe)
c.1661G>T (p.Cys554Phe)
3g.38603812C=CA1358584893SCN5Ac.1790G= (p.Cys597=)
c.1661G= (p.Cys554=)
3g.38603812C>GCA352146153SCN5Ac.1790G>C (p.Cys597Ser)
c.1661G>C (p.Cys554Ser)
COSMIC COSMIC COSMIC
3g.38603812C>TCA352146154SCN5Ac.1790G>A (p.Cys597Tyr)
c.1661G>A (p.Cys554Tyr)
dbSNP gnomAD v2 gnomAD v4
3g.38603813A=CA1358584895SCN5Ac.1789T= (p.Cys597=)
c.1660T= (p.Cys554=)
3g.38603813A>CCA352146157SCN5Ac.1789T>G (p.Cys597Gly)
c.1660T>G (p.Cys554Gly)
dbSNP gnomAD v2
3g.38603813A>GCA352146155SCN5Ac.1789T>C (p.Cys597Arg)
c.1660T>C (p.Cys554Arg)
3g.38603813A>TCA352146156SCN5Ac.1789T>A (p.Cys597Ser)
c.1660T>A (p.Cys554Ser)
3g.38603814G>ACA433332902SCN5Ac.1788C>T (p.Asp596=)
c.1659C>T (p.Asp553=)
ClinVar
3g.38603814G>CCA352146158SCN5Ac.1788C>G (p.Asp596Glu)
c.1659C>G (p.Asp553Glu)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38603814G=CA1358584897SCN5Ac.1788C= (p.Asp596=)
c.1659C= (p.Asp553=)
3g.38603814G>TCA352146160SCN5Ac.1788C>A (p.Asp596Glu)
c.1659C>A (p.Asp553Glu)
3g.38603815T>ACA352146161SCN5Ac.1787A>T (p.Asp596Val)
c.1658A>T (p.Asp553Val)
3g.38603815T>CCA015362SCN5Ac.1787A>G (p.Asp596Gly)
c.1658A>G (p.Asp553Gly)
ClinVar dbSNP
3g.38603815T>GCA352146163SCN5Ac.1787A>C (p.Asp596Ala)
c.1658A>C (p.Asp553Ala)
3g.38603815T=CA1358584899SCN5Ac.1787A= (p.Asp596=)
c.1658A= (p.Asp553=)
3g.38603816C>ACA352146166SCN5Ac.1786G>T (p.Asp596Tyr)
c.1657G>T (p.Asp553Tyr)
gnomAD v4
3g.38603816C>GCA352146169SCN5Ac.1786G>C (p.Asp596His)
c.1657G>C (p.Asp553His)
3g.38603816C>TCA352146167SCN5Ac.1786G>A (p.Asp596Asn)
c.1657G>A (p.Asp553Asn)
3g.38603817C>ACA433332908SCN5Ac.1785G>T (p.Val595=)
c.1656G>T (p.Val552=)
3g.38603817C>GCA433332909SCN5Ac.1785G>C (p.Val595=)
c.1656G>C (p.Val552=)
3g.38603817C>TCA433332913SCN5Ac.1785G>A (p.Val595=)
c.1656G>A (p.Val552=)
gnomAD v4
3g.38603818A=CA1358584903SCN5Ac.1784T= (p.Val595=)
c.1655T= (p.Val552=)
3g.38603818A>CCA352146171SCN5Ac.1784T>G (p.Val595Gly)
c.1655T>G (p.Val552Gly)
3g.38603818A>GCA352146173SCN5Ac.1784T>C (p.Val595Ala)
c.1655T>C (p.Val552Ala)
ClinVar dbSNP gnomAD v4
3g.38603818A>TCA352146175SCN5Ac.1784T>A (p.Val595Glu)
c.1655T>A (p.Val552Glu)
3g.38603819C>ACA352146177SCN5Ac.1783G>T (p.Val595Leu)
c.1654G>T (p.Val552Leu)
ClinVar dbSNP
3g.38603819C>GCA352146178SCN5Ac.1783G>C (p.Val595Leu)
c.1654G>C (p.Val552Leu)
3g.38603819C>TCA352146181SCN5Ac.1783G>A (p.Val595Met)
c.1654G>A (p.Val552Met)
gnomAD v4
3g.38603820A>CCA433332915SCN5Ac.1782T>G (p.Thr594=)
c.1653T>G (p.Thr551=)
3g.38603820A>GCA433332916SCN5Ac.1782T>C (p.Thr594=)
c.1653T>C (p.Thr551=)
3g.38603820A>TCA433332917SCN5Ac.1782T>A (p.Thr594=)
c.1653T>A (p.Thr551=)
3g.38603821G>ACA352146184SCN5Ac.1781C>T (p.Thr594Ile)
c.1652C>T (p.Thr551Ile)
ClinVar gnomAD v4
3g.38603821G>CCA352146185SCN5Ac.1781C>G (p.Thr594Ser)
c.1652C>G (p.Thr551Ser)
3g.38603821G>TCA352146186SCN5Ac.1781C>A (p.Thr594Asn)
c.1652C>A (p.Thr551Asn)
3g.38603822T>ACA352146187SCN5Ac.1780A>T (p.Thr594Ser)
c.1651A>T (p.Thr551Ser)
3g.38603822T>CCA352146188SCN5Ac.1780A>G (p.Thr594Ala)
c.1651A>G (p.Thr551Ala)
3g.38603822T>GCA352146189SCN5Ac.1780A>C (p.Thr594Pro)
c.1651A>C (p.Thr551Pro)
3g.38603823G>ACA433332924SCN5Ac.1779C>T (p.Ser593=)
c.1650C>T (p.Ser550=)
3g.38603823G>CCA352146191SCN5Ac.1779C>G (p.Ser593Arg)
c.1650C>G (p.Ser550Arg)
3g.38603823G>TCA352146190SCN5Ac.1779C>A (p.Ser593Arg)
c.1650C>A (p.Ser550Arg)
3g.38603824C>ACA352146193SCN5Ac.1778G>T (p.Ser593Ile)
c.1649G>T (p.Ser550Ile)
3g.38603824C>GCA352146197SCN5Ac.1778G>C (p.Ser593Thr)
c.1649G>C (p.Ser550Thr)
3g.38603824C>TCA352146195SCN5Ac.1778G>A (p.Ser593Asn)
c.1649G>A (p.Ser550Asn)
3g.38603825T>ACA352146200SCN5Ac.1777A>T (p.Ser593Cys)
c.1648A>T (p.Ser550Cys)
3g.38603825T>CCA352146201SCN5Ac.1777A>G (p.Ser593Gly)
c.1648A>G (p.Ser550Gly)
gnomAD v4
3g.38603825T>GCA352146203SCN5Ac.1777A>C (p.Ser593Arg)
c.1648A>C (p.Ser550Arg)
3g.38603826G>ACA058802SCN5Ac.1776C>T (p.Asn592=)
c.1647C>T (p.Asn549=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38603826G>CCA058791SCN5Ac.1776C>G (p.Asn592Lys)
c.1647C>G (p.Asn549Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38603826G=CA1358584906SCN5Ac.1776C= (p.Asn592=)
c.1647C= (p.Asn549=)

Number of alleles fetched