G21D (p.Gly21Asp) variant of CETP (P11597)
G21D (p.Gly21Asp) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
G21D (p.Gly21Asp) variant details
- p.Gly21Asp
- gnomAD rs1282799611
- Missense
- Variant Prioritization Score for Impact Estimate 0.0762
- REVEL 0.07
- CADD 2.69
- PolyPhen-2 0.16
- SIFT 0.36
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available