L37F (p.Leu37Phe) variant of CETP (P11597)
L37F (p.Leu37Phe) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
L37F (p.Leu37Phe) variant details
- p.Leu37Phe
- ExAC rs773933829
- gnomAD rs773933829
- Missense
- Variant Prioritization Score for Impact Estimate 0.202
- REVEL 0.05
- CADD 11.70
- PolyPhen-2 0.24
- SIFT 0.15
- Most common in the South Asian population (allele frequency 5.8e-05)
- Structural context available