| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32340146C>T | CA023241 | BRCA2 | c.5791C>T (p.Gln1931Ter) c.5422C>T (p.Gln1808Ter) n.5791C>T | ClinVar dbSNP |
| 13 | g.32340146C>G | CA387787175 | BRCA2 | c.5791C>G (p.Gln1931Glu) c.5422C>G (p.Gln1808Glu) n.5791C>G | ClinVar dbSNP |
| 13 | g.32340146C>A | CA387787174 | BRCA2 | c.5791C>A (p.Gln1931Lys) c.5422C>A (p.Gln1808Lys) n.5791C>A | ClinVar dbSNP |