| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32339648A>G | CA387784792 | BRCA2 | c.5293A>G (p.Lys1765Glu) c.4924A>G (p.Lys1642Glu) n.5293A>G | ClinVar dbSNP |
| 13 | g.32339648A>T | CA10586073 | BRCA2 | c.5293A>T (p.Lys1765Ter) c.4924A>T (p.Lys1642Ter) n.5293A>T | ClinVar dbSNP |