A36T (p.Ala36Thr) variant of CETP (P11597)
A36T (p.Ala36Thr) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
A36T (p.Ala36Thr) variant details
- p.Ala36Thr
- TOPMed rs1365954946
- gnomAD rs1365954946
- Missense
- Variant Prioritization Score for Impact Estimate 0.273
- REVEL 0.22
- CADD 25.10
- PolyPhen-2 0.94
- SIFT 0.00
- Most common in the East Asian population (allele frequency 0.00018)
- Structural context available