I39V (p.Ile39Val) variant of CYP2C8 (Cytochrome P450 2C8)
I39V (p.Ile39Val) in CYP2C8 (Cytochrome P450 2C8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
I39V (p.Ile39Val) variant details
- p.Ile39Val
- TOPMed rs1420452597
- gnomAD rs1420452597
- Missense
- Variant Prioritization Score for Impact Estimate 0.0766
- REVEL 0.08
- CADD 2.12
- PolyPhen-2 0.01
- SIFT 0.26
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available