| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32340380C>A | CA387787763 | BRCA2 | c.6025C>A (p.Gln2009Lys) c.5656C>A (p.Gln1886Lys) n.6025C>A | dbSNP |
| 13 | g.32340380C>G | CA387787765 | BRCA2 | c.6025C>G (p.Gln2009Glu) c.5656C>G (p.Gln1886Glu) n.6025C>G | dbSNP |
| 13 | g.32340380C>T | CA023540 | BRCA2 | c.6025C>T (p.Gln2009Ter) c.5656C>T (p.Gln1886Ter) n.6025C>T | ClinVar dbSNP |