S26F (p.Ser26Phe) variant of HLA-B (P01889)
S26F (p.Ser26Phe) in HLA-B (P01889) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
S26F (p.Ser26Phe) variant details
- p.Ser26Phe
- Ensembl rs151341087
- Missense
- Variant Prioritization Score for Impact Estimate 0.181
- REVEL 0.12
- CADD 24.20
- PolyPhen-2 1.00
- SIFT 0.02
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.5e-05)
- Structural context available