P58R (p.Pro58Arg) variant of CETP (P11597)
P58R (p.Pro58Arg) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
P58R (p.Pro58Arg) variant details
- p.Pro58Arg
- gnomAD rs890161478
- Missense
- Variant Prioritization Score for Impact Estimate 0.413
- REVEL 0.40
- CADD 22.70
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Middle Eastern population (allele frequency 0.00017)
- Structural context available