| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32326146del | CA16613909 | BRCA2 | c.471del (p.Lys157AsnfsTer15) c.102del (p.Lys34AsnfsTer15) n.342del c.*250del (n.*250del) n.669del n.471del | ClinVar dbSNP |
| 13 | g.32326146G= | CA2082750279 | BRCA2 | c.471G= (p.Lys157=) c.102G= (p.Lys34=) n.342G= c.*250G= (n.*250G=) n.669G= n.471G= | dbSNP dbSNP |