| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32337900_32337901del | CA018299 | BRCA2 | c.3545_3546del (p.Phe1182Ter) c.3176_3177del (p.Phe1059Ter) n.3545_3546del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337901del | CA10589210 | BRCA2 | c.3546del (p.Phe1182LeufsTer15) c.3177del (p.Phe1059LeufsTer15) n.3546del | ClinVar dbSNP |