Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32356514G>A | CA025130 | BRCA2 | c.7522G>A (p.Gly2508Ser) c.7153G>A (p.Gly2385Ser) c.87G>A n.7522G>A c.7426G>A (p.Gly2476Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.32356514G>C | CA387743535 | BRCA2 | c.7522G>C (p.Gly2508Arg) c.7153G>C (p.Gly2385Arg) c.87G>C n.7522G>C c.7426G>C (p.Gly2476Arg) | ClinVar dbSNP |
13 | g.32356514G>T | CA387743536 | BRCA2 | c.7522G>T (p.Gly2508Cys) c.7153G>T (p.Gly2385Cys) c.87G>T n.7522G>T c.7426G>T (p.Gly2476Cys) | dbSNP |