| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32338795T>C | CA16606788 | BRCA2 | c.4440T>C (p.Tyr1480=) c.4071T>C (p.Tyr1357=) n.4440T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32338795T>A | CA387781332 | BRCA2 | c.4440T>A (p.Tyr1480Ter) c.4071T>A (p.Tyr1357Ter) n.4440T>A | dbSNP |
| 13 | g.32338795T>G | CA020187 | BRCA2 | c.4440T>G (p.Tyr1480Ter) c.4071T>G (p.Tyr1357Ter) n.4440T>G | ClinVar dbSNP |