| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.49474074A>T | CA376721328 | ERCC6 | c.2551T>A (p.Trp851Arg) n.2629T>A c.2392T>A (p.Trp798Arg) c.*847T>A (n.*847T>A) c.661T>A (p.Trp221Arg) c.383T>A | ClinVar dbSNP |
| 10 | g.49474074A>G | CA277416 | ERCC6 | c.2551T>C (p.Trp851Arg) n.2629T>C c.2392T>C (p.Trp798Arg) c.*847T>C (n.*847T>C) c.661T>C (p.Trp221Arg) c.383T>C | ClinVar dbSNP |