Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38603808A=CA1358584882SCN5Ac.1794T= (p.Asn598=)
c.1665T= (p.Asn555=)
3g.38603808A>CCA352146128SCN5Ac.1794T>G (p.Asn598Lys)
c.1665T>G (p.Asn555Lys)
3g.38603808A>GCA433332893SCN5Ac.1794T>C (p.Asn598=)
c.1665T>C (p.Asn555=)
ClinVar dbSNP gnomAD v4
3g.38603808A>TCA352146130SCN5Ac.1794T>A (p.Asn598Lys)
c.1665T>A (p.Asn555Lys)
3g.38603809T>ACA352146131SCN5Ac.1793A>T (p.Asn598Ile)
c.1664A>T (p.Asn555Ile)
3g.38603809T>CCA352146132SCN5Ac.1793A>G (p.Asn598Ser)
c.1664A>G (p.Asn555Ser)
ClinVar dbSNP gnomAD v4
3g.38603809T>GCA352146133SCN5Ac.1793A>C (p.Asn598Thr)
c.1664A>C (p.Asn555Thr)
3g.38603809T=CA1358584885SCN5Ac.1793A= (p.Asn598=)
c.1664A= (p.Asn555=)
3g.38603810dupCA2839660821SCN5Ac.1793dup (p.Asn598LysfsTer?)
c.1664dup (p.Asn555LysfsTer?)
3g.38603810T>ACA352146141SCN5Ac.1792A>T (p.Asn598Tyr)
c.1663A>T (p.Asn555Tyr)
3g.38603810T>CCA352146143SCN5Ac.1792A>G (p.Asn598Asp)
c.1663A>G (p.Asn555Asp)
ClinVar
3g.38603810T>GCA352146135SCN5Ac.1792A>C (p.Asn598His)
c.1663A>C (p.Asn555His)
3g.38603811G>ACA433332897SCN5Ac.1791C>T (p.Cys597=)
c.1662C>T (p.Cys554=)
gnomAD v4
3g.38603811G>CCA352146147SCN5Ac.1791C>G (p.Cys597Trp)
c.1662C>G (p.Cys554Trp)
3g.38603811G=CA1358584890SCN5Ac.1791C= (p.Cys597=)
c.1662C= (p.Cys554=)
3g.38603811G>TCA352146149SCN5Ac.1791C>A (p.Cys597Ter)
c.1662C>A (p.Cys554Ter)
dbSNP
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)

Number of alleles fetched