Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.124398082A>G | CA113987 | OAT | c.1180T>C (p.Cys394Arg) n.690T>C c.766T>C (p.Cys256Arg) c.859T>C (p.Cys287Arg) c.580T>C (p.Cys194Arg) | ClinVar dbSNP gnomAD v4 COSMIC |
10 | g.124398082A= | CA1942335692 | OAT | c.1180T= (p.Cys394=) n.690T= c.766T= (p.Cys256=) c.859T= (p.Cys287=) c.580T= (p.Cys194=) | dbSNP |