V39M (p.Val39Met) variant of CETP (P11597)
V39M (p.Val39Met) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data, published literature, and structural context.
V39M (p.Val39Met) variant details
- p.Val39Met
- gnomAD 16-56962094-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.252
- REVEL 0.09
- CADD 23.80
- PolyPhen-2 0.92
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available