S97G (p.Ser97Gly) variant of CD8B (P10966)
S97G (p.Ser97Gly) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
S97G (p.Ser97Gly) variant details
- p.Ser97Gly
- ExAC rs779620836
- TOPMed rs779620836
- gnomAD rs779620836
- Missense
- Variant Prioritization Score for Impact Estimate 0.187
- REVEL 0.21
- MetaLR 0.31
- MetaSVM -0.60
- CADD 2.50
- PolyPhen-2 0.60
- SIFT 0.18
- Most common in the Latino/Admixed American population (allele frequency 0.00013)
- Structural context available