G78R (p.Gly78Arg) variant of CD8B (P10966)
G78R (p.Gly78Arg) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
G78R (p.Gly78Arg) variant details
- p.Gly78Arg
- gnomAD rs1402775866
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- REVEL 0.16
- MetaLR 0.37
- MetaSVM -0.63
- CADD 5.19
- PolyPhen-2 0.81
- SIFT 0.24
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.7e-05)
- Structural context available