Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38622446C>ACA352154682SCN5Ac.436G>T (p.Val146Leu)
n.631G>T
3g.38622446C=CA1358593014SCN5Ac.436G= (p.Val146=)
n.631G=
3g.38622446C>GCA352154681SCN5Ac.436G>C (p.Val146Leu)
n.631G>C
3g.38622446C>TCA018183SCN5Ac.436G>A (p.Val146Met)
n.631G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38622447G>ACA018176SCN5Ac.435C>T (p.Cys145=)
n.630C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38622447G>CCA352154688SCN5Ac.435C>G (p.Cys145Trp)
n.630C>G
3g.38622447G=CA1358593015SCN5Ac.435C= (p.Cys145=)
n.630C=
3g.38622447G>TCA352154690SCN5Ac.435C>A (p.Cys145Ter)
n.630C>A
ClinVar dbSNP
3g.38622448C>ACA352154692SCN5Ac.434G>T (p.Cys145Phe)
n.629G>T
gnomAD v4
3g.38622448C=CA1358593016SCN5Ac.434G= (p.Cys145=)
n.629G=
3g.38622448C>GCA352154694SCN5Ac.434G>C (p.Cys145Ser)
n.629G>C
3g.38622448C>TCA352154696SCN5Ac.434G>A (p.Cys145Tyr)
n.629G>A
dbSNP
3g.38622449A=CA1358593017SCN5Ac.433T= (p.Cys145=)
n.628T=
3g.38622449A>CCA352154701SCN5Ac.433T>G (p.Cys145Gly)
n.628T>G
3g.38622449A>GCA352154698SCN5Ac.433T>C (p.Cys145Arg)
n.628T>C
ClinVar dbSNP
3g.38622449A>TCA352154700SCN5Ac.433T>A (p.Cys145Ser)
n.628T>A
3g.38622450G>ACA433139168SCN5Ac.432C>T (p.Asn144=)
n.627C>T
3g.38622450G>CCA352154703SCN5Ac.432C>G (p.Asn144Lys)
n.627C>G
3g.38622450G>TCA352154705SCN5Ac.432C>A (p.Asn144Lys)
n.627C>A
3g.38622451T>ACA352154707SCN5Ac.431A>T (p.Asn144Ile)
n.626A>T
3g.38622451T>CCA352154709SCN5Ac.431A>G (p.Asn144Ser)
n.626A>G
gnomAD v4
3g.38622451T>GCA352154711SCN5Ac.431A>C (p.Asn144Thr)
n.626A>C
ClinVar gnomAD v4
3g.38622452T>ACA352154714SCN5Ac.430A>T (p.Asn144Tyr)
n.625A>T
3g.38622452T>CCA352154718SCN5Ac.430A>G (p.Asn144Asp)
n.625A>G
3g.38622452T>GCA352154716SCN5Ac.430A>C (p.Asn144His)
n.625A>C
3g.38622453G>ACA433139169SCN5Ac.429C>T (p.Thr143=)
n.624C>T
3g.38622453G>CCA433139171SCN5Ac.429C>G (p.Thr143=)
n.624C>G
3g.38622453G>TCA433139170SCN5Ac.429C>A (p.Thr143=)
n.624C>A
3g.38622454delCA2586972100SCN5Ac.429del (p.Asn144ThrfsTer?)
n.624del
3g.38622454G>ACA352154721SCN5Ac.428C>T (p.Thr143Ile)
n.623C>T
3g.38622454G>CCA352154723SCN5Ac.428C>G (p.Thr143Ser)
n.623C>G
3g.38622454G>TCA352154725SCN5Ac.428C>A (p.Thr143Asn)
n.623C>A
gnomAD v4
3g.38622455T>ACA352154728SCN5Ac.427A>T (p.Thr143Ser)
n.622A>T
3g.38622455T>CCA063020SCN5Ac.427A>G (p.Thr143Ala)
n.622A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38622455T>GCA352154731SCN5Ac.427A>C (p.Thr143Pro)
n.622A>C
3g.38622455T=CA1358593018SCN5Ac.427A= (p.Thr143=)
n.622A=
3g.38622456G>ACA433139172SCN5Ac.426C>T (p.Leu142=)
n.621C>T
3g.38622456G>CCA433139173SCN5Ac.426C>G (p.Leu142=)
n.621C>G
3g.38622456G>TCA433139174SCN5Ac.426C>A (p.Leu142=)
n.621C>A
3g.38622457A>CCA352154734SCN5Ac.425T>G (p.Leu142Arg)
n.620T>G
3g.38622457A>GCA352154736SCN5Ac.425T>C (p.Leu142Pro)
n.620T>C
3g.38622457A>TCA352154738SCN5Ac.425T>A (p.Leu142His)
n.620T>A
3g.38622458G>ACA352154743SCN5Ac.424C>T (p.Leu142Phe)
n.619C>T
ClinVar dbSNP
3g.38622458G>CCA352154745SCN5Ac.424C>G (p.Leu142Val)
n.619C>G
3g.38622458G=CA1358593019SCN5Ac.424C= (p.Leu142=)
n.619C=
3g.38622458G>TCA352154747SCN5Ac.424C>A (p.Leu142Ile)
n.619C>A
3g.38622459G>ACA433139175SCN5Ac.423C>T (p.Ile141=)
n.618C>T
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
3g.38622459G>CCA352154750SCN5Ac.423C>G (p.Ile141Met)
n.618C>G
3g.38622459G=CA1358593020SCN5Ac.423C= (p.Ile141=)
n.618C=
3g.38622459G>TCA433139176SCN5Ac.423C>A (p.Ile141=)
n.618C>A
ClinVar

Number of alleles fetched