| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.124398061C>A | CA113990 | OAT | c.1201G>T (p.Gly401Ter) n.711G>T c.787G>T (p.Gly263Ter) c.880G>T (p.Gly294Ter) c.601G>T (p.Gly201Ter) | ClinVar dbSNP gnomAD v4 |
| 10 | g.124398061C= | CA1942335684 | OAT | c.1201G= (p.Gly401=) n.711G= c.787G= (p.Gly263=) c.880G= (p.Gly294=) c.601G= (p.Gly201=) | dbSNP |