A36D (p.Ala36Asp) variant of CETP (P11597)
A36D (p.Ala36Asp) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
A36D (p.Ala36Asp) variant details
- p.Ala36Asp
- gnomAD 16-56962086-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.405
- REVEL 0.34
- CADD 24.20
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available