R30W (p.Arg30Trp) variant of HLA-B (P01889)
R30W (p.Arg30Trp) in HLA-B (P01889) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
R30W (p.Arg30Trp) variant details
- p.Arg30Trp
- Ensembl rs2113751791
- Missense
- Variant Prioritization Score for Impact Estimate 0.288
- REVEL 0.15
- CADD 23.80
- PolyPhen-2 0.99
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.4e-06)
- Structural context available