| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32357846G>T | CA387745455 | BRCA2 | c.7722G>T (p.Trp2574Cys) c.7353G>T (p.Trp2451Cys) c.189G>T (p.Trp63Cys) c.287G>T n.7722G>T c.7626G>T (p.Trp2542Cys) | ClinVar dbSNP |
| 13 | g.32357846G>C | CA387745454 | BRCA2 | c.7722G>C (p.Trp2574Cys) c.7353G>C (p.Trp2451Cys) c.189G>C (p.Trp63Cys) c.287G>C n.7722G>C c.7626G>C (p.Trp2542Cys) | dbSNP |
| 13 | g.32357846G>A | CA16614212 | BRCA2 | c.7722G>A (p.Trp2574Ter) c.7353G>A (p.Trp2451Ter) c.189G>A (p.Trp63Ter) c.287G>A n.7722G>A c.7626G>A (p.Trp2542Ter) | ClinVar dbSNP |