Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32363190A>G | CA387748557 | BRCA2 | c.7988A>G (p.Glu2663Gly) c.7619A>G (p.Glu2540Gly) c.455A>G (p.Glu152Gly) c.7996A>G (n.7996A>G) c.553A>G c.7892A>G (p.Glu2631Gly) | ClinVar dbSNP |
13 | g.32363190A>T | CA025385 | BRCA2 | c.7988A>T (p.Glu2663Val) c.7619A>T (p.Glu2540Val) c.455A>T (p.Glu152Val) c.7996A>T (n.7996A>T) c.553A>T c.7892A>T (p.Glu2631Val) | ClinVar dbSNP gnomAD v4 |