| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32339641T>G | CA387784772 | BRCA2 | c.5286T>G (p.Tyr1762Ter) c.4917T>G (p.Tyr1639Ter) n.5286T>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32339641T>A | CA021955 | BRCA2 | c.5286T>A (p.Tyr1762Ter) c.4917T>A (p.Tyr1639Ter) n.5286T>A | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339641T= | CA2082821336 | BRCA2 | c.5286T= (p.Tyr1762=) c.4917T= (p.Tyr1639=) n.5286T= | dbSNP |