| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32357911G>T | CA387746014 | BRCA2 | c.7787G>T (p.Gly2596Val) c.7418G>T (p.Gly2473Val) c.254G>T (p.Gly85Val) c.352G>T n.7787G>T c.7691G>T (p.Gly2564Val) | ClinVar dbSNP |
| 13 | g.32357911G>C | CA387746017 | BRCA2 | c.7787G>C (p.Gly2596Ala) c.7418G>C (p.Gly2473Ala) c.254G>C (p.Gly85Ala) c.352G>C n.7787G>C c.7691G>C (p.Gly2564Ala) | ClinVar dbSNP |
| 13 | g.32357911G>A | CA16619771 | BRCA2 | c.7787G>A (p.Gly2596Glu) c.7418G>A (p.Gly2473Glu) c.254G>A (p.Gly85Glu) c.352G>A n.7787G>A c.7691G>A (p.Gly2564Glu) | ClinVar dbSNP |