L2Q (p.Leu2Gln) variant of HLA-B (P01889)
L2Q (p.Leu2Gln) in HLA-B (P01889) is a missense change. The available record places it in the context of in allele B*13:02, allele B*15:01, allele B*18:01, allele B*27:01, allele B*27:0. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
L2Q (p.Leu2Gln) variant details
- p.Leu2Gln
- 1000Genomes rs9266206
- ExAC rs9266206
- gnomAD rs9266206
- in allele B*13:02, allele B*15:01, allele B*18:01, allele B*27:01, allele B*27:0
- Missense
- Variant Prioritization Score for Impact Estimate 0.208
- REVEL 0.26
- CADD 9.36
- PolyPhen-2 0.00
- SIFT 0.43
- Population evidence available
- Structural context available