A16G (p.Ala16Gly) variant of HLA-B (P01889)
A16G (p.Ala16Gly) in HLA-B (P01889) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
A16G (p.Ala16Gly) variant details
- p.Ala16Gly
- ExAC rs45585233
- gnomAD rs45585233
- Missense
- Variant Prioritization Score for Impact Estimate 0.31
- REVEL 0.15
- CADD 20.60
- PolyPhen-2 0.33
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.5e-06)
- Structural context available