A51G (p.Ala51Gly) variant of CETP (P11597)
A51G (p.Ala51Gly) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data, published literature, and structural context.
A51G (p.Ala51Gly) variant details
- p.Ala51Gly
- gnomAD 16-56963043-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.207
- REVEL 0.14
- CADD 18.90
- PolyPhen-2 0.45
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available