| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32340524G>T | CA023712 | BRCA2 | c.6169G>T (p.Gly2057Ter) c.5800G>T (p.Gly1934Ter) n.6169G>T | ClinVar dbSNP |
| 13 | g.32340524G>A | CA387788354 | BRCA2 | c.6169G>A (p.Gly2057Arg) c.5800G>A (p.Gly1934Arg) n.6169G>A | ClinVar dbSNP |
| 13 | g.32340524G= | CA2082811153 | BRCA2 | c.6169G= (p.Gly2057=) c.5800G= (p.Gly1934=) n.6169G= | dbSNP |