Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.40015416T>C | CA460788976 | IDO2 | c.1038T>C (p.Tyr346=) n.3289T>C n.665T>C c.1077T>C (p.Tyr359=) | dbSNP |
8 | g.40015416T>A | CA4725373 | IDO2 | c.1038T>A (p.Tyr346Ter) n.3289T>A n.665T>A c.1077T>A (p.Tyr359Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.40015416T= | CA1778257328 | IDO2 | c.1038T= (p.Tyr346=) n.3289T= n.665T= c.1077T= (p.Tyr359=) | dbSNP |