| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32376717del | CA025779 | BRCA2 | c.8680del (p.Gln2894LysfsTer15) c.*47del (n.*47del) c.8311del (p.Gln2771LysfsTer15) c.*242del (n.*242del) c.1147del (p.Gln383LysfsTer15) n.807del c.8688del (n.8688del) c.1558del c.242del (n.242del) c.8584del (p.Gln2862LysfsTer15) | ClinVar dbSNP |
| 13 | g.32376717C= | CA2082828710 | BRCA2 | c.8680C= (p.Gln2894=) c.*47C= (n.*47C=) c.8311C= (p.Gln2771=) c.*242C= (n.*242C=) c.1147C= (p.Gln383=) n.807C= c.8688C= (n.8688C=) c.1558C= c.242C= (n.242C=) c.8584C= (p.Gln2862=) | dbSNP dbSNP |