| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32338628del | CA16613968 | BRCA2 | c.4273del (p.Asp1425IlefsTer23) c.3904del (p.Asp1302IlefsTer23) n.4273del | ClinVar dbSNP |
| 13 | g.32338628G= | CA3200933606 | BRCA2 | c.4273G= (p.Asp1425=) c.3904G= (p.Asp1302=) n.4273G= | dbSNP dbSNP |