S37A (p.Ser37Ala) variant of HLA-B (P01889)
S37A (p.Ser37Ala) 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.
S37A (p.Ser37Ala) variant details
- p.Ser37Ala
- gnomAD rs41552612
- Missense
- Variant Prioritization Score for Impact Estimate 0.336
- REVEL 0.23
- CADD 24.50
- PolyPhen-2 0.99
- SIFT 0.00
- Population evidence available
- Structural context available