S37P (p.Ser37Pro) variant of HLA-B (P01889)
S37P (p.Ser37Pro) 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.
S37P (p.Ser37Pro) variant details
- p.Ser37Pro
- gnomAD rs41552612
- Missense
- Variant Prioritization Score for Impact Estimate 0.314
- REVEL 0.19
- CADD 25.20
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.3e-06)
- Structural context available