Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38609776C>ACA352150397SCN5Ac.892G>T (p.Gly298Cys)
c.763G>T (p.Gly255Cys)
3g.38609776C=CA1358587645SCN5Ac.892G= (p.Gly298=)
c.763G= (p.Gly255=)
3g.38609776C>GCA352150398SCN5Ac.892G>C (p.Gly298Arg)
c.763G>C (p.Gly255Arg)
3g.38609776C>TCA019920SCN5Ac.892G>A (p.Gly298Ser)
c.763G>A (p.Gly255Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38609777G>ACA065862SCN5Ac.891C>T (p.Asp297=)
c.762C>T (p.Asp254=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38609777G>CCA352150399SCN5Ac.891C>G (p.Asp297Glu)
c.762C>G (p.Asp254Glu)
3g.38609777G=CA1358587646SCN5Ac.891C= (p.Asp297=)
c.762C= (p.Asp254=)
3g.38609777G>TCA352150400SCN5Ac.891C>A (p.Asp297Glu)
c.762C>A (p.Asp254Glu)
3g.38609778T>ACA352150401SCN5Ac.890A>T (p.Asp297Val)
c.761A>T (p.Asp254Val)
3g.38609778T>CCA352150402SCN5Ac.890A>G (p.Asp297Gly)
c.761A>G (p.Asp254Gly)
3g.38609778T>GCA352150403SCN5Ac.890A>C (p.Asp297Ala)
c.761A>C (p.Asp254Ala)
3g.38609779C>ACA352150404SCN5Ac.889G>T (p.Asp297Tyr)
c.760G>T (p.Asp254Tyr)
3g.38609779C=CA1358587647SCN5Ac.889G= (p.Asp297=)
c.760G= (p.Asp254=)
3g.38609779C>GCA352150405SCN5Ac.889G>C (p.Asp297His)
c.760G>C (p.Asp254His)
3g.38609779C>TCA019914SCN5Ac.889G>A (p.Asp297Asn)
c.760G>A (p.Asp254Asn)
ClinVar dbSNP gnomAD v4
3g.38609780G>ACA065857SCN5Ac.888C>T (p.Ala296=)
c.759C>T (p.Ala253=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38609780G>CCA065853SCN5Ac.888C>G (p.Ala296=)
c.759C>G (p.Ala253=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38609780G=CA1358587648SCN5Ac.888C= (p.Ala296=)
c.759C= (p.Ala253=)
3g.38609780G>TCA433138201SCN5Ac.888C>A (p.Ala296=)
c.759C>A (p.Ala253=)
3g.38609780_38609781insCACA2665116061SCN5Ac.887_888insTG (p.Asp297AlafsTer?)
c.758_759insTG (p.Asp254AlafsTer?)
gnomAD v4
3g.38609781G>ACA352150406SCN5Ac.887C>T (p.Ala296Val)
c.758C>T (p.Ala253Val)
3g.38609781G>CCA352150407SCN5Ac.887C>G (p.Ala296Gly)
c.758C>G (p.Ala253Gly)
3g.38609781G>TCA352150408SCN5Ac.887C>A (p.Ala296Asp)
c.758C>A (p.Ala253Asp)
3g.38609782C>ACA352150409SCN5Ac.886G>T (p.Ala296Ser)
c.757G>T (p.Ala253Ser)
3g.38609782C>GCA352150410SCN5Ac.886G>C (p.Ala296Pro)
c.757G>C (p.Ala253Pro)
3g.38609782C>TCA352150411SCN5Ac.886G>A (p.Ala296Thr)
c.757G>A (p.Ala253Thr)
3g.38609783C>ACA352150412SCN5Ac.885G>T (p.Glu295Asp)
c.756G>T (p.Glu252Asp)
3g.38609783C=CA1358587649SCN5Ac.885G= (p.Glu295=)
c.756G= (p.Glu252=)
3g.38609783C>GCA352150413SCN5Ac.885G>C (p.Glu295Asp)
c.756G>C (p.Glu252Asp)
3g.38609783C>TCA019908SCN5Ac.885G>A (p.Glu295=)
c.756G>A (p.Glu252=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38609784T>ACA352150414SCN5Ac.884A>T (p.Glu295Val)
c.755A>T (p.Glu252Val)
3g.38609784T>CCA352150415SCN5Ac.884A>G (p.Glu295Gly)
c.755A>G (p.Glu252Gly)
3g.38609784T>GCA352150416SCN5Ac.884A>C (p.Glu295Ala)
c.755A>C (p.Glu252Ala)
3g.38609785C>ACA352150417SCN5Ac.883G>T (p.Glu295Ter)
c.754G>T (p.Glu252Ter)
3g.38609785C=CA1358587650SCN5Ac.883G= (p.Glu295=)
c.754G= (p.Glu252=)
3g.38609785C>GCA352150418SCN5Ac.883G>C (p.Glu295Gln)
c.754G>C (p.Glu252Gln)
3g.38609785C>TCA065839SCN5Ac.883G>A (p.Glu295Lys)
c.754G>A (p.Glu252Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38609786C>ACA433138207SCN5Ac.882G>T (p.Val294=)
c.753G>T (p.Val251=)
3g.38609786C>GCA433138208SCN5Ac.882G>C (p.Val294=)
c.753G>C (p.Val251=)
3g.38609786C>TCA433138209SCN5Ac.882G>A (p.Val294=)
c.753G>A (p.Val251=)
3g.38609787A>CCA352150419SCN5Ac.881T>G (p.Val294Gly)
c.752T>G (p.Val251Gly)
3g.38609787A>GCA352150421SCN5Ac.881T>C (p.Val294Ala)
c.752T>C (p.Val251Ala)
gnomAD v4
3g.38609787A>TCA352150420SCN5Ac.881T>A (p.Val294Glu)
c.752T>A (p.Val251Glu)
3g.38609788C>ACA352150422SCN5Ac.880G>T (p.Val294Leu)
c.751G>T (p.Val251Leu)
gnomAD v2 gnomAD v4
3g.38609788C=CA1358587651SCN5Ac.880G= (p.Val294=)
c.751G= (p.Val251=)
3g.38609788C>GCA352150423SCN5Ac.880G>C (p.Val294Leu)
c.751G>C (p.Val251Leu)
3g.38609788C>TCA019903SCN5Ac.880G>A (p.Val294Met)
c.751G>A (p.Val251Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38609789G>ACA065817SCN5Ac.879C>T (p.Ser293=)
c.750C>T (p.Ser250=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38609789G>CCA433138216SCN5Ac.879C>G (p.Ser293=)
c.750C>G (p.Ser250=)
3g.38609789G=CA1358587652SCN5Ac.879C= (p.Ser293=)
c.750C= (p.Ser250=)

Number of alleles fetched