| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32337334G>T | CA387774564 | BRCA2 | c.2979G>T (p.Trp993Cys) c.2610G>T (p.Trp870Cys) n.2979G>T | ClinVar dbSNP |
| 13 | g.32337334G>A | CA016943 | BRCA2 | c.2979G>A (p.Trp993Ter) c.2610G>A (p.Trp870Ter) n.2979G>A | ClinVar dbSNP |
| 13 | g.32337334G>C | CA387774563 | BRCA2 | c.2979G>C (p.Trp993Cys) c.2610G>C (p.Trp870Cys) n.2979G>C | dbSNP COSMIC COSMIC |