| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32338829A>T | CA16042139 | BRCA2 | c.4474A>T (p.Lys1492Ter) c.4105A>T (p.Lys1369Ter) n.4474A>T | ClinVar dbSNP |
| 13 | g.32338829A>G | CA387781472 | BRCA2 | c.4474A>G (p.Lys1492Glu) c.4105A>G (p.Lys1369Glu) n.4474A>G | ClinVar dbSNP |