| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32362625T>A | CA025327 | BRCA2 | c.7908T>A (p.Cys2636Ter) c.7539T>A (p.Cys2513Ter) c.375T>A (p.Cys125Ter) c.7916T>A (p.Val2639Glu) c.473T>A n.7916T>A c.7812T>A (p.Cys2604Ter) | ClinVar dbSNP |
| 13 | g.32362625T>G | CA387747164 | BRCA2 | c.7908T>G (p.Cys2636Trp) c.7539T>G (p.Cys2513Trp) c.375T>G (p.Cys125Trp) c.7916T>G (p.Val2639Gly) c.473T>G n.7916T>G c.7812T>G (p.Cys2604Trp) | dbSNP |