| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32363369G>C | CA025482 | BRCA2 | c.8167G>C (p.Asp2723His) c.7798G>C (p.Asp2600His) c.634G>C (p.Asp212His) c.8175G>C (n.8175G>C) c.732G>C c.8071G>C (p.Asp2691His) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32363369G>A | CA387749585 | BRCA2 | c.8167G>A (p.Asp2723Asn) c.7798G>A (p.Asp2600Asn) c.634G>A (p.Asp212Asn) c.8175G>A (n.8175G>A) c.732G>A c.8071G>A (p.Asp2691Asn) | ClinVar dbSNP |