W20G (p.Trp20Gly) variant of CD3E (P07766)
W20G (p.Trp20Gly) in CD3E (P07766) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Immunodeficiency 18. The record also includes structural context.
W20G (p.Trp20Gly) variant details
- p.Trp20Gly
- rs2496826882
- ClinGen CA382779997
- ClinVar RCV003042187
- Uncertain significance
- Immunodeficiency 18
- Missense
- ClinVar: Uncertain significance (Immunodeficiency 18)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available