H16H (p.His16His) variant of CETP (P11597)
H16H (p.His16His) in CETP (P11597) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
H16H (p.His16His) variant details
- p.His16His
- rs767475225
- gnomAD 16-56962027-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0845
- CADD 0.65
- Most common in the South Asian population (allele frequency 3.5e-05)
- Structural context available
- Literature evidence available