E39G (p.Glu39Gly) variant of RAG1 (P15918)
E39G (p.Glu39Gly) in RAG1 (P15918) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
E39G (p.Glu39Gly) variant details
- p.Glu39Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.33
- MetaSVM -0.49
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available