V38M (p.Val38Met) variant of CD80 (P33681)
V38M (p.Val38Met) in CD80 (P33681) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
V38M (p.Val38Met) variant details
- p.Val38Met
- ESP rs146886200
- TOPMed rs146886200
- gnomAD rs146886200
- Missense
- Variant Prioritization Score for Impact Estimate 0.289
- REVEL 0.27
- MetaLR 0.43
- MetaSVM -0.49
- CADD 17.00
- PolyPhen-2 0.80
- SIFT 0.04
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available