T34A (p.Thr34Ala) variant of HLA-B (P01889)
T34A (p.Thr34Ala) in HLA-B (P01889) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
T34A (p.Thr34Ala) variant details
- p.Thr34Ala
- 1000Genomes rs774891894
- ExAC rs774891894
- gnomAD rs774891894
- Missense
- Variant Prioritization Score for Impact Estimate 0.188
- REVEL 0.16
- CADD 22.00
- PolyPhen-2 0.02
- SIFT 0.02
- Most common in the East Asian population (allele frequency 8.2e-05)
- Structural context available