Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32355262dup | CA025059 | BRCA2 | c.7409dup (p.Thr2471HisfsTer4) c.7040dup (p.Thr2348HisfsTer4) n.7409dup c.7313dup (p.Thr2439HisfsTer4) | ClinVar dbSNP |
13 | g.32355261_32355262del | CA025058 | BRCA2 | c.7408_7409del (p.Phe2470HisfsTer4) c.7039_7040del (p.Phe2347HisfsTer4) n.7408_7409del c.7312_7313del (p.Phe2438HisfsTer4) | ClinVar dbSNP |