| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.91724248C>T | CA118707 | ROR2 | c.2246G>A (p.Trp749Ter) c.1826G>A (p.Trp609Ter) n.2714G>A c.1043G>A (p.Trp348Ter) c.2237G>A (p.Trp746Ter) | ClinVar dbSNP |
| 9 | g.91724248C= | CA1863922439 | ROR2 | c.2246G= (p.Trp749=) c.1826G= (p.Trp609=) n.2714G= c.1043G= (p.Trp348=) c.2237G= (p.Trp746=) | dbSNP |