F46V (p.Phe46Val) variant of RAG2 (P55895)
F46V (p.Phe46Val) in RAG2 (P55895) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes experimental measurements and structural context.
F46V (p.Phe46Val) variant details
- p.Phe46Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available
- RAG2 Recombination activating protein 2, PHD domain domainome 1.0: score -0.113