| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32336837T>C | CA16614121 | BRCA2 | c.2482T>C (p.Tyr828His) c.2113T>C (p.Tyr705His) n.2482T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32336837T= | CA2082808929 | BRCA2 | c.2482T= (p.Tyr828=) c.2113T= (p.Tyr705=) n.2482T= | dbSNP |