L38L (p.Leu38Leu) variant of CETP (P11597)
L38L (p.Leu38Leu) in CETP (P11597) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.54 / 1. The record also includes population frequency data, published literature, and structural context.
L38L (p.Leu38Leu) variant details
- p.Leu38Leu
- gnomAD 16-56962091-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.543
- CADD 4.75
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available
- Literature evidence available