V38L (p.Val38Leu) variant of CYP2C9 (Cytochrome P450 2C9)
V38L (p.Val38Leu) in CYP2C9 (Cytochrome P450 2C9) 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, published literature, and structural context.
V38L (p.Val38Leu) variant details
- p.Val38Leu
- gnomAD 10-94938794-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.08
- REVEL 0.10
- CADD 0.19
- PolyPhen-2 0.00
- SIFT 0.12
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available