| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32357881G>A | CA025259 | BRCA2 | c.7757G>A (p.Trp2586Ter) c.7388G>A (p.Trp2463Ter) c.224G>A (p.Trp75Ter) c.322G>A n.7757G>A c.7661G>A (p.Trp2554Ter) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32357881G>T | CA387745814 | BRCA2 | c.7757G>T (p.Trp2586Leu) c.7388G>T (p.Trp2463Leu) c.224G>T (p.Trp75Leu) c.322G>T n.7757G>T c.7661G>T (p.Trp2554Leu) | dbSNP |