| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32357916G>T | CA387746039 | BRCA2 | c.7792G>T (p.Glu2598Ter) c.7423G>T (p.Glu2475Ter) c.259G>T (p.Glu87Ter) c.357G>T n.7792G>T c.7696G>T (p.Glu2566Ter) | ClinVar dbSNP |
| 13 | g.32357916G>C | CA387746037 | BRCA2 | c.7792G>C (p.Glu2598Gln) c.7423G>C (p.Glu2475Gln) c.259G>C (p.Glu87Gln) c.357G>C n.7792G>C c.7696G>C (p.Glu2566Gln) | dbSNP |
| 13 | g.32357916G>A | CA387746035 | BRCA2 | c.7792G>A (p.Glu2598Lys) c.7423G>A (p.Glu2475Lys) c.259G>A (p.Glu87Lys) c.357G>A n.7792G>A c.7696G>A (p.Glu2566Lys) | dbSNP |