H16N (p.His16Asn) variant of CETP (P11597)
H16N (p.His16Asn) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
H16N (p.His16Asn) variant details
- p.His16Asn
- gnomAD rs1389424544
- Missense
- Variant Prioritization Score for Impact Estimate 0.132
- REVEL 0.02
- CADD 3.20
- PolyPhen-2 0.00
- SIFT 0.47
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available