| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.49482860G>A | CA199585 | ERCC6 | c.1996C>T (p.Arg666Cys) n.2074C>T c.1837C>T (p.Arg613Cys) c.*388C>T (n.*388C>T) c.106C>T (p.Arg36Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.49482860G= | CA1908760621 | ERCC6 | c.1996C= (p.Arg666=) n.2074C= c.1837C= (p.Arg613=) c.*388C= (n.*388C=) c.106C= (p.Arg36=) | dbSNP |