| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32363529T>G | CA025575 | BRCA2 | c.8327T>G (p.Leu2776Ter) c.7958T>G (p.Leu2653Ter) c.794T>G (p.Leu265Ter) c.8335T>G (n.8335T>G) c.892T>G c.8231T>G (p.Leu2744Ter) | ClinVar dbSNP gnomAD v4 |
| 13 | g.32363529T= | CA2082837562 | BRCA2 | c.8327T= (p.Leu2776=) c.7958T= (p.Leu2653=) c.794T= (p.Leu265=) c.8335T= (n.8335T=) c.892T= c.8231T= (p.Leu2744=) | dbSNP |