Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.91724229G>A | CA5120436 | ROR2 | c.2265C>T (p.Tyr755=) c.1845C>T (p.Tyr615=) n.2733C>T c.1062C>T (p.Tyr354=) c.2256C>T (p.Tyr752=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91724229G>T | CA118705 | ROR2 | c.2265C>A (p.Tyr755Ter) c.1845C>A (p.Tyr615Ter) n.2733C>A c.1062C>A (p.Tyr354Ter) c.2256C>A (p.Tyr752Ter) | ClinVar dbSNP gnomAD v4 |