| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32336810C>A | CA387772299 | BRCA2 | c.2455C>A (p.Gln819Lys) c.2086C>A (p.Gln696Lys) n.2455C>A | dbSNP |
| 13 | g.32336810C>G | CA387772300 | BRCA2 | c.2455C>G (p.Gln819Glu) c.2086C>G (p.Gln696Glu) n.2455C>G | ClinVar dbSNP |
| 13 | g.32336810C>T | CA015343 | BRCA2 | c.2455C>T (p.Gln819Ter) c.2086C>T (p.Gln696Ter) n.2455C>T | ClinVar dbSNP |