Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38622446C>A | CA352154682 | SCN5A | c.436G>T (p.Val146Leu) n.631G>T | |
3 | g.38622446C= | CA1358593014 | SCN5A | c.436G= (p.Val146=) n.631G= | |
3 | g.38622446C>G | CA352154681 | SCN5A | c.436G>C (p.Val146Leu) n.631G>C | |
3 | g.38622446C>T | CA018183 | SCN5A | c.436G>A (p.Val146Met) n.631G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
3 | g.38622447G>A | CA018176 | SCN5A | c.435C>T (p.Cys145=) n.630C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
3 | g.38622447G>C | CA352154688 | SCN5A | c.435C>G (p.Cys145Trp) n.630C>G | |
3 | g.38622447G= | CA1358593015 | SCN5A | c.435C= (p.Cys145=) n.630C= | |
3 | g.38622447G>T | CA352154690 | SCN5A | c.435C>A (p.Cys145Ter) n.630C>A | ClinVar dbSNP |
3 | g.38622448C>A | CA352154692 | SCN5A | c.434G>T (p.Cys145Phe) n.629G>T | gnomAD v4 |
3 | g.38622448C= | CA1358593016 | SCN5A | c.434G= (p.Cys145=) n.629G= | |
3 | g.38622448C>G | CA352154694 | SCN5A | c.434G>C (p.Cys145Ser) n.629G>C | |
3 | g.38622448C>T | CA352154696 | SCN5A | c.434G>A (p.Cys145Tyr) n.629G>A | dbSNP |
3 | g.38622449A= | CA1358593017 | SCN5A | c.433T= (p.Cys145=) n.628T= | |
3 | g.38622449A>C | CA352154701 | SCN5A | c.433T>G (p.Cys145Gly) n.628T>G | |
3 | g.38622449A>G | CA352154698 | SCN5A | c.433T>C (p.Cys145Arg) n.628T>C | ClinVar dbSNP |
3 | g.38622449A>T | CA352154700 | SCN5A | c.433T>A (p.Cys145Ser) n.628T>A | |
3 | g.38622450G>A | CA433139168 | SCN5A | c.432C>T (p.Asn144=) n.627C>T | |
3 | g.38622450G>C | CA352154703 | SCN5A | c.432C>G (p.Asn144Lys) n.627C>G | |
3 | g.38622450G>T | CA352154705 | SCN5A | c.432C>A (p.Asn144Lys) n.627C>A | |
3 | g.38622451T>A | CA352154707 | SCN5A | c.431A>T (p.Asn144Ile) n.626A>T | |
3 | g.38622451T>C | CA352154709 | SCN5A | c.431A>G (p.Asn144Ser) n.626A>G | gnomAD v4 |
3 | g.38622451T>G | CA352154711 | SCN5A | c.431A>C (p.Asn144Thr) n.626A>C | ClinVar gnomAD v4 |
3 | g.38622452T>A | CA352154714 | SCN5A | c.430A>T (p.Asn144Tyr) n.625A>T | |
3 | g.38622452T>C | CA352154718 | SCN5A | c.430A>G (p.Asn144Asp) n.625A>G | |
3 | g.38622452T>G | CA352154716 | SCN5A | c.430A>C (p.Asn144His) n.625A>C | |
3 | g.38622453G>A | CA433139169 | SCN5A | c.429C>T (p.Thr143=) n.624C>T | |
3 | g.38622453G>C | CA433139171 | SCN5A | c.429C>G (p.Thr143=) n.624C>G | |
3 | g.38622453G>T | CA433139170 | SCN5A | c.429C>A (p.Thr143=) n.624C>A | |
3 | g.38622454del | CA2586972100 | SCN5A | c.429del (p.Asn144ThrfsTer?) n.624del | |
3 | g.38622454G>A | CA352154721 | SCN5A | c.428C>T (p.Thr143Ile) n.623C>T | |
3 | g.38622454G>C | CA352154723 | SCN5A | c.428C>G (p.Thr143Ser) n.623C>G | |
3 | g.38622454G>T | CA352154725 | SCN5A | c.428C>A (p.Thr143Asn) n.623C>A | gnomAD v4 |
3 | g.38622455T>A | CA352154728 | SCN5A | c.427A>T (p.Thr143Ser) n.622A>T | |
3 | g.38622455T>C | CA063020 | SCN5A | c.427A>G (p.Thr143Ala) n.622A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.38622455T>G | CA352154731 | SCN5A | c.427A>C (p.Thr143Pro) n.622A>C | |
3 | g.38622455T= | CA1358593018 | SCN5A | c.427A= (p.Thr143=) n.622A= | |
3 | g.38622456G>A | CA433139172 | SCN5A | c.426C>T (p.Leu142=) n.621C>T | |
3 | g.38622456G>C | CA433139173 | SCN5A | c.426C>G (p.Leu142=) n.621C>G | |
3 | g.38622456G>T | CA433139174 | SCN5A | c.426C>A (p.Leu142=) n.621C>A | |
3 | g.38622457A>C | CA352154734 | SCN5A | c.425T>G (p.Leu142Arg) n.620T>G | |
3 | g.38622457A>G | CA352154736 | SCN5A | c.425T>C (p.Leu142Pro) n.620T>C | |
3 | g.38622457A>T | CA352154738 | SCN5A | c.425T>A (p.Leu142His) n.620T>A | |
3 | g.38622458G>A | CA352154743 | SCN5A | c.424C>T (p.Leu142Phe) n.619C>T | ClinVar dbSNP |
3 | g.38622458G>C | CA352154745 | SCN5A | c.424C>G (p.Leu142Val) n.619C>G | |
3 | g.38622458G= | CA1358593019 | SCN5A | c.424C= (p.Leu142=) n.619C= | |
3 | g.38622458G>T | CA352154747 | SCN5A | c.424C>A (p.Leu142Ile) n.619C>A | |
3 | g.38622459G>A | CA433139175 | SCN5A | c.423C>T (p.Ile141=) n.618C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC |
3 | g.38622459G>C | CA352154750 | SCN5A | c.423C>G (p.Ile141Met) n.618C>G | |
3 | g.38622459G= | CA1358593020 | SCN5A | c.423C= (p.Ile141=) n.618C= | |
3 | g.38622459G>T | CA433139176 | SCN5A | c.423C>A (p.Ile141=) n.618C>A | ClinVar |