G127V (p.Gly127Val) variant of CD8B (P10966)
G127V (p.Gly127Val) in CD8B (P10966) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The record also includes structural context.
G127V (p.Gly127Val) variant details
- p.Gly127Val
- rs2466679432
- ClinGen CA347580656
- ClinVar RCV004111534
- Uncertain significance
- not specified
- Missense
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available