G21G (p.Gly21Gly) variant of CETP (P11597)
G21G (p.Gly21Gly) in CETP (P11597) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
G21G (p.Gly21Gly) variant details
- p.Gly21Gly
- gnomAD 16-56962042-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0899
- CADD 1.30
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available