Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.91724247C>T | CA118709 | ROR2 | c.2247G>A (p.Trp749Ter) c.1827G>A (p.Trp609Ter) n.2715G>A c.1044G>A (p.Trp348Ter) c.2238G>A (p.Trp746Ter) | ClinVar dbSNP |
9 | g.91724247C= | CA1863922431 | ROR2 | c.2247G= (p.Trp749=) c.1827G= (p.Trp609=) n.2715G= c.1044G= (p.Trp348=) c.2238G= (p.Trp746=) | dbSNP |