| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.107947388A>G | CA130342 | CYP2U1 | c.1139A>G (p.Glu380Gly) c.512A>G (p.Glu171Gly) c.1193A>G (p.Glu398Gly) c.503A>G (p.Glu168Gly) n.156-36839T>C n.530+31332T>C | ClinVar dbSNP |
| 4 | g.107947388A= | CA1483927712 | CYP2U1 | c.1139A= (p.Glu380=) c.512A= (p.Glu171=) c.1193A= (p.Glu398=) c.503A= (p.Glu168=) n.156-36839T= n.530+31332T= | dbSNP |