| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32337797C>T | CA018022 | BRCA2 | c.3442C>T (p.Gln1148Ter) c.3073C>T (p.Gln1025Ter) n.3442C>T | ClinVar dbSNP |
| 13 | g.32337797C>G | CA387776630 | BRCA2 | c.3442C>G (p.Gln1148Glu) c.3073C>G (p.Gln1025Glu) n.3442C>G | dbSNP |
| 13 | g.32337797C>A | CA387776628 | BRCA2 | c.3442C>A (p.Gln1148Lys) c.3073C>A (p.Gln1025Lys) n.3442C>A | dbSNP |