| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32362573G>C | CA025310 | BRCA2 | c.7856G>C (p.Trp2619Ser) c.7487G>C (p.Trp2496Ser) c.323G>C (p.Trp108Ser) c.7864G>C (p.Gly2622Arg) c.421G>C n.7864G>C c.7760G>C (p.Trp2587Ser) | ClinVar dbSNP |
| 13 | g.32362573G>A | CA025309 | BRCA2 | c.7856G>A (p.Trp2619Ter) c.7487G>A (p.Trp2496Ter) c.323G>A (p.Trp108Ter) c.7864G>A (p.Gly2622Arg) c.421G>A n.7864G>A c.7760G>A (p.Trp2587Ter) | ClinVar dbSNP |
| 13 | g.32362573G>T | CA387747059 | BRCA2 | c.7856G>T (p.Trp2619Leu) c.7487G>T (p.Trp2496Leu) c.323G>T (p.Trp108Leu) c.7864G>T (p.Gly2622Trp) c.421G>T n.7864G>T c.7760G>T (p.Trp2587Leu) | dbSNP |