Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.9759390A>T | CA226180 | GPR143 | c.397T>A (p.Trp133Arg) c.145T>A (p.Trp49Arg) n.5T>A | ClinVar dbSNP |
X | g.9759390A>G | CA226181 | GPR143 | c.397T>C (p.Trp133Arg) c.145T>C (p.Trp49Arg) n.5T>C | ClinVar dbSNP |
X | g.9759390A= | CA2415030080 | GPR143 | c.397T= (p.Trp133=) c.145T= (p.Trp49=) n.5T= | dbSNP |
X | g.9759390A>C | CA411998925 | GPR143 | c.397T>G (p.Trp133Gly) c.145T>G (p.Trp49Gly) n.5T>G | ClinVar dbSNP |