V26L (p.Val26Leu) variant of CD8A (P01732)
V26L (p.Val26Leu) in CD8A (P01732) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
V26L (p.Val26Leu) variant details
- p.Val26Leu
- rs771549955
- ClinGen CA1751277
- ClinVar RCV002922335
- ExAC rs771549955
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.0925
- REVEL 0.04
- MetaLR 0.07
- MetaSVM -1.07
- CADD 7.45
- PolyPhen-2 0.00
- SIFT 0.15
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available