G27R (p.Gly27Arg) variant of CETP (P11597)
G27R (p.Gly27Arg) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
G27R (p.Gly27Arg) variant details
- p.Gly27Arg
- Ensembl rs2141989701
- Missense
- Variant Prioritization Score for Impact Estimate 0.357
- REVEL 0.26
- CADD 23.30
- Most common in the HGDP:BEDOUIN population (allele frequency 0.012)
- Structural context available