P39T (p.Pro39Thr) variant of HLA-B (P01889)
P39T (p.Pro39Thr) in HLA-B (P01889) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
P39T (p.Pro39Thr) variant details
- p.Pro39Thr
- Ensembl rs151341099
- Missense
- Variant Prioritization Score for Impact Estimate 0.342
- REVEL 0.20
- CADD 24.90
- PolyPhen-2 0.77
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 2.6e-06)
- Structural context available