N14N (p.Asn14Asn) variant of CETP (P11597)
N14N (p.Asn14Asn) in CETP (P11597) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
N14N (p.Asn14Asn) variant details
- p.Asn14Asn
- rs763683938
- gnomAD 16-56962021-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.112
- CADD 4.42
- Most common in the Middle Eastern population (allele frequency 0.00017)
- Structural context available
- Literature evidence available