V38E (p.Val38Glu) variant of CYP2C9 (Cytochrome P450 2C9)
V38E (p.Val38Glu) in CYP2C9 (Cytochrome P450 2C9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
V38E (p.Val38Glu) variant details
- p.Val38Glu
- gnomAD rs1414284836
- Missense
- Variant Prioritization Score for Impact Estimate 0.463
- REVEL 0.43
- CADD 22.80
- PolyPhen-2 0.63
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)
- Structural context available