V39E (p.Val39Glu) variant of CETP (P11597)
V39E (p.Val39Glu) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data, published literature, and structural context.
V39E (p.Val39Glu) variant details
- p.Val39Glu
- gnomAD 16-56962095-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.233
- REVEL 0.22
- CADD 23.10
- PolyPhen-2 0.93
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available
- Literature evidence available