G91D (p.Gly91Asp) variant of CD8A (P01732)
G91D (p.Gly91Asp) in CD8A (P01732) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
G91D (p.Gly91Asp) variant details
- p.Gly91Asp
- TOPMed rs1400434555
- gnomAD rs1400434555
- Missense
- Variant Prioritization Score for Impact Estimate 0.416
- REVEL 0.29
- AlphaMissense 0.92
- MetaLR 0.89
- MetaSVM 0.98
- CADD 22.40
- PolyPhen-2 1.00
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)
- Structural context available