| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32363421T>A | CA025524 | BRCA2 | c.8219T>A (p.Leu2740Ter) c.7850T>A (p.Leu2617Ter) c.686T>A (p.Leu229Ter) c.8227T>A (n.8227T>A) c.784T>A c.8123T>A (p.Leu2708Ter) | ClinVar dbSNP |
| 13 | g.32363421T= | CA2082836536 | BRCA2 | c.8219T= (p.Leu2740=) c.7850T= (p.Leu2617=) c.686T= (p.Leu229=) c.8227T= (n.8227T=) c.784T= c.8123T= (p.Leu2708=) | dbSNP |