G13V (p.Gly13Val) variant of CETP (P11597)
G13V (p.Gly13Val) 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.
G13V (p.Gly13Val) variant details
- p.Gly13Val
- gnomAD 16-56962017-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.255
- REVEL 0.18
- CADD 22.70
- PolyPhen-2 0.99
- SIFT 0.01
- Population evidence available
- Structural context available
- Literature evidence available