Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38581265C>T | CA016602 | SCN5A | c.2894G>A (p.Arg965His) c.2765G>A (p.Arg922His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
3 | g.38581265C>A | CA016609 | SCN5A | c.2894G>T (p.Arg965Leu) c.2765G>T (p.Arg922Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.38581265C= | CA1358574550 | SCN5A | c.2894G= (p.Arg965=) c.2765G= (p.Arg922=) | dbSNP |