P39L (p.Pro39Leu) variant of HLA-B (P01889)
P39L (p.Pro39Leu) 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.
P39L (p.Pro39Leu) variant details
- p.Pro39Leu
- Ensembl rs281864587
- Missense
- Variant Prioritization Score for Impact Estimate 0.34
- REVEL 0.19
- CADD 26.10
- PolyPhen-2 0.95
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.3e-06)
- Structural context available