E110D (p.Glu110Asp) variant of CD8A (P01732)
E110D (p.Glu110Asp) in CD8A (P01732) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data.
E110D (p.Glu110Asp) variant details
- p.Glu110Asp
- NCI-TCGA TCGA novel
- ExAC rs756864143
- gnomAD rs756864143
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.191
- REVEL 0.24
- MetaLR 0.22
- MetaSVM -0.76
- CADD 1.55
- PolyPhen-2 0.29
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the 1KG:MSL population (allele frequency 0.013)