Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38581266G>A | CA016594 | SCN5A | c.2893C>T (p.Arg965Cys) c.2764C>T (p.Arg922Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.38581266G>C | CA061002 | SCN5A | c.2893C>G (p.Arg965Gly) c.2764C>G (p.Arg922Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.38581266G= | CA1358574552 | SCN5A | c.2893C= (p.Arg965=) c.2764C= (p.Arg922=) | dbSNP |