V38M (p.Val38Met) variant of CD276 (CD276 antigen)
V38M (p.Val38Met) in CD276 (CD276 antigen) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
V38M (p.Val38Met) variant details
- p.Val38Met
- ExAC rs774478067
- TOPMed rs774478067
- gnomAD rs774478067
- Missense
- Variant Prioritization Score for Impact Estimate 0.439
- REVEL 0.20
- CADD 25.50
- PolyPhen-2 0.95
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 4.5e-05)
- Structural context available