| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32341007del | CA645294075 | BRCA2 | c.6652del (p.Asp2218IlefsTer11) c.6283del (p.Asp2095IlefsTer11) n.6652del | ClinVar dbSNP |
| 13 | g.32341007G= | CA2082816769 | BRCA2 | c.6652G= (p.Asp2218=) c.6283G= (p.Asp2095=) n.6652G= | dbSNP dbSNP dbSNP |