| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32336300C>T | CA014000 | BRCA2 | c.1945C>T (p.Gln649Ter) c.1576C>T (p.Gln526Ter) n.1945C>T | ClinVar dbSNP |
| 13 | g.32336300C>A | CA387768388 | BRCA2 | c.1945C>A (p.Gln649Lys) c.1576C>A (p.Gln526Lys) n.1945C>A | ClinVar dbSNP |
| 13 | g.32336300C>G | CA387768390 | BRCA2 | c.1945C>G (p.Gln649Glu) c.1576C>G (p.Gln526Glu) n.1945C>G | dbSNP |