| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32341011C>A | CA387790423 | BRCA2 | c.6656C>A (p.Ser2219Ter) c.6287C>A (p.Ser2096Ter) n.6656C>A | ClinVar dbSNP |
| 13 | g.32341011C>T | CA387790426 | BRCA2 | c.6656C>T (p.Ser2219Leu) c.6287C>T (p.Ser2096Leu) n.6656C>T | dbSNP |
| 13 | g.32341011C>G | CA024263 | BRCA2 | c.6656C>G (p.Ser2219Ter) c.6287C>G (p.Ser2096Ter) n.6656C>G | ClinVar dbSNP |