Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32363259T>C | CA025427 | BRCA2 | c.8057T>C (p.Leu2686Pro) c.7688T>C (p.Leu2563Pro) c.524T>C (p.Leu175Pro) c.8065T>C (n.8065T>C) c.622T>C c.7961T>C (p.Leu2654Pro) | ClinVar dbSNP gnomAD v4 |
13 | g.32363259T>G | CA387749102 | BRCA2 | c.8057T>G (p.Leu2686Arg) c.7688T>G (p.Leu2563Arg) c.524T>G (p.Leu175Arg) c.8065T>G (n.8065T>G) c.622T>G c.7961T>G (p.Leu2654Arg) | ClinVar dbSNP |
13 | g.32363259T>A | CA387749100 | BRCA2 | c.8057T>A (p.Leu2686His) c.7688T>A (p.Leu2563His) c.524T>A (p.Leu175His) c.8065T>A (n.8065T>A) c.622T>A c.7961T>A (p.Leu2654His) | dbSNP |