Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.152649108A>T | CA16618433 | XRCC2 | c.209T>A (p.Leu70Ter) c.377T>A (p.Leu126Ter) n.399T>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.152649108A>C | CA370198828 | XRCC2 | c.209T>G (p.Leu70Ter) c.377T>G (p.Leu126Ter) n.399T>G | ClinVar dbSNP gnomAD v4 |