| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32339338T>C | CA483438310 | BRCA2 | c.4983T>C (p.Tyr1661=) c.4614T>C (p.Tyr1538=) n.4983T>C | ClinVar dbSNP gnomAD v4 |
| 13 | g.32339338T>G | CA16616709 | BRCA2 | c.4983T>G (p.Tyr1661Ter) c.4614T>G (p.Tyr1538Ter) n.4983T>G | ClinVar dbSNP |
| 13 | g.32339338T>A | CA387783868 | BRCA2 | c.4983T>A (p.Tyr1661Ter) c.4614T>A (p.Tyr1538Ter) n.4983T>A | dbSNP gnomAD v4 |