Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.91737400G>T | CA5120962 | ROR2 | c.613C>A (p.Arg205=) c.193C>A (p.Arg65=) n.1081C>A c.604C>A (p.Arg202=) n.856C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.91737400G>A | CA254147 | ROR2 | c.613C>T (p.Arg205Ter) c.193C>T (p.Arg65Ter) n.1081C>T c.604C>T (p.Arg202Ter) n.856C>T | ClinVar dbSNP gnomAD v4 |