N41Y (p.Asn41Tyr) variant of CETP (P11597)
N41Y (p.Asn41Tyr) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, published literature, and structural context.
N41Y (p.Asn41Tyr) variant details
- p.Asn41Tyr
- gnomAD 16-56963012-A-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.341
- REVEL 0.33
- CADD 24.00
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available