| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32337638C>T | CA017706 | BRCA2 | c.3283C>T (p.Gln1095Ter) c.2914C>T (p.Gln972Ter) n.3283C>T | ClinVar dbSNP |
| 13 | g.32337638C>G | CA387776099 | BRCA2 | c.3283C>G (p.Gln1095Glu) c.2914C>G (p.Gln972Glu) n.3283C>G | ClinVar dbSNP |
| 13 | g.32337638C>A | CA387776098 | BRCA2 | c.3283C>A (p.Gln1095Lys) c.2914C>A (p.Gln972Lys) n.3283C>A | ClinVar dbSNP |