Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.43551574T>C | CA9488516 | XRCC1 | c.1196A>G (p.Gln399Arg) c.1103A>G (p.Gln368Arg) c.806A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.43551574T>G | CA406203108 | XRCC1 | c.1196A>C (p.Gln399Pro) c.1103A>C (p.Gln368Pro) c.806A>C | dbSNP |
19 | g.43551574T= | CA2337551252 | XRCC1 | c.1196A= (p.Gln399=) c.1103A= (p.Gln368=) c.806A= | dbSNP |