| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32340000C>A | CA022818 | BRCA2 | c.5645C>A (p.Ser1882Ter) c.5276C>A (p.Ser1759Ter) n.5645C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 13 | g.32340000C>G | CA022825 | BRCA2 | c.5645C>G (p.Ser1882Ter) c.5276C>G (p.Ser1759Ter) n.5645C>G | ClinVar dbSNP |
| 13 | g.32340000C= | CA2082825727 | BRCA2 | c.5645C= (p.Ser1882=) c.5276C= (p.Ser1759=) n.5645C= | dbSNP |