| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32336569T>G | CA387770613 | BRCA2 | c.2214T>G (p.Cys738Trp) c.1845T>G (p.Cys615Trp) n.2214T>G | dbSNP |
| 13 | g.32336569T>C | CA483436848 | BRCA2 | c.2214T>C (p.Cys738=) c.1845T>C (p.Cys615=) n.2214T>C | dbSNP |
| 13 | g.32336569T>A | CA014637 | BRCA2 | c.2214T>A (p.Cys738Ter) c.1845T>A (p.Cys615Ter) n.2214T>A | ClinVar dbSNP |