| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32340929del | CA16614340 | BRCA2 | c.6574del (p.Met2192TrpfsTer14) c.6205del (p.Met2069TrpfsTer14) n.6574del | ClinVar dbSNP |
| 13 | g.32340929dup | CA2825002114 | BRCA2 | c.6574dup (p.Met2192AsnfsTer5) c.6205dup (p.Met2069AsnfsTer5) n.6574dup | ClinVar dbSNP |