H16R (p.His16Arg) variant of CETP (P11597)
H16R (p.His16Arg) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.05 / 1. The record also includes population frequency data and structural context.
H16R (p.His16Arg) variant details
- p.His16Arg
- gnomAD rs1303090767
- Missense
- Variant Prioritization Score for Impact Estimate 0.0456
- REVEL 0.02
- CADD 2.59
- PolyPhen-2 0.00
- SIFT 0.54
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available