L13F (p.Leu13Phe) variant of HLA-B (P01889)
L13F (p.Leu13Phe) in HLA-B (P01889) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
L13F (p.Leu13Phe) variant details
- p.Leu13Phe
- gnomAD rs1290354847
- Missense
- Variant Prioritization Score for Impact Estimate 0.316
- REVEL 0.13
- CADD 25.10
- PolyPhen-2 1.00
- SIFT 0.01
- Population evidence available
- Structural context available