L11P (p.Leu11Pro) variant of HLA-B (P01889)
L11P (p.Leu11Pro) 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.
L11P (p.Leu11Pro) variant details
- p.Leu11Pro
- ExAC rs756534089
- gnomAD rs756534089
- Missense
- Variant Prioritization Score for Impact Estimate 0.343
- REVEL 0.18
- CADD 32.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-06)
- Structural context available