| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32355033A>T | CA024928 | BRCA2 | c.7180A>T (p.Arg2394Ter) c.6811A>T (p.Arg2271Ter) n.7180A>T c.7084A>T (p.Arg2362Ter) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32355033A>G | CA387739584 | BRCA2 | c.7180A>G (p.Arg2394Gly) c.6811A>G (p.Arg2271Gly) n.7180A>G c.7084A>G (p.Arg2362Gly) | dbSNP |