Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32336961C>T | CA015810 | BRCA2 | c.2606C>T (p.Ser869Leu) c.2237C>T (p.Ser746Leu) n.2606C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
13 | g.32336961C>G | CA10586061 | BRCA2 | c.2606C>G (p.Ser869Ter) c.2237C>G (p.Ser746Ter) n.2606C>G | ClinVar dbSNP gnomAD v4 |
13 | g.32336961C>A | CA387772640 | BRCA2 | c.2606C>A (p.Ser869Ter) c.2237C>A (p.Ser746Ter) n.2606C>A | dbSNP |