Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32338447dup | CA10589240 | BRCA2 | c.4092dup (p.Cys1365MetfsTer3) c.3723dup (p.Cys1242MetfsTer3) n.4092dup | ClinVar dbSNP |
13 | g.32338447_32338448insAA | CA10579601 | BRCA2 | c.4092_4093insAA (p.Cys1365AsnfsTer10) c.3723_3724insAA (p.Cys1242AsnfsTer10) n.4092_4093insAA | ClinVar dbSNP |