S56N (p.Ser56Asn) variant of CETP (P11597)
S56N (p.Ser56Asn) in CETP (P11597) is a missense 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.
S56N (p.Ser56Asn) variant details
- p.Ser56Asn
- gnomAD 16-56963058-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0821
- REVEL 0.01
- CADD 0.37
- PolyPhen-2 0.00
- SIFT 0.41
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available