T79A (p.Thr79Ala) variant of RAG2 (P55895)
T79A (p.Thr79Ala) in RAG2 (P55895) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
T79A (p.Thr79Ala) variant details
- p.Thr79Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available