D59H (p.Asp59His) variant of CETP (P11597)
D59H (p.Asp59His) 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.
D59H (p.Asp59His) variant details
- p.Asp59His
- TOPMed rs1271404748
- gnomAD rs1271404748
- Missense
- Variant Prioritization Score for Impact Estimate 0.201
- REVEL 0.10
- CADD 19.20
- PolyPhen-2 0.90
- SIFT 0.01
- Most common in the REMAINING population (allele frequency 3.3e-05)
- Structural context available