S97R (p.Ser97Arg) variant of CD8B (P10966)
S97R (p.Ser97Arg) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
S97R (p.Ser97Arg) variant details
- p.Ser97Arg
- cosmic curated COSV58927
- Missense
- Variant Prioritization Score for Impact Estimate 0.17
- REVEL 0.15
- MetaLR 0.28
- MetaSVM -0.91
- CADD 1.16
- PolyPhen-2 0.14
- SIFT 0.17
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available