V38V (p.Val38Val) variant of CYP2C9 (Cytochrome P450 2C9)
V38V (p.Val38Val) in CYP2C9 (Cytochrome P450 2C9) is a synonymous 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.
V38V (p.Val38Val) variant details
- p.Val38Val
- rs2031308785
- gnomAD 10-94938796-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0809
- CADD 0.03
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available