| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32337513T>G | CA017322 | BRCA2 | c.3158T>G (p.Leu1053Ter) c.2789T>G (p.Leu930Ter) n.3158T>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32337513T>A | CA387775778 | BRCA2 | c.3158T>A (p.Leu1053Ter) c.2789T>A (p.Leu930Ter) n.3158T>A | ClinVar dbSNP |
| 13 | g.32337513T= | CA2082814831 | BRCA2 | c.3158T= (p.Leu1053=) c.2789T= (p.Leu930=) n.3158T= | dbSNP |