V29E (p.Val29Glu) variant of CETP (P11597)
V29E (p.Val29Glu) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
V29E (p.Val29Glu) variant details
- p.Val29Glu
- gnomAD rs2056027061
- Missense
- Variant Prioritization Score for Impact Estimate 0.391
- REVEL 0.26
- CADD 24.60
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available