| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32340094T>G | CA387786957 | BRCA2 | c.5739T>G (p.Cys1913Trp) c.5370T>G (p.Cys1790Trp) n.5739T>G | dbSNP |
| 13 | g.32340094T>C | CA483438896 | BRCA2 | c.5739T>C (p.Cys1913=) c.5370T>C (p.Cys1790=) n.5739T>C | ClinVar dbSNP |
| 13 | g.32340094T>A | CA023111 | BRCA2 | c.5739T>A (p.Cys1913Ter) c.5370T>A (p.Cys1790Ter) n.5739T>A | ClinVar dbSNP |