A76V (p.Ala76Val) variant of RAG2 (P55895)
A76V (p.Ala76Val) 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.
A76V (p.Ala76Val) variant details
- p.Ala76Val
- NCI-TCGA Cosmic COSV5755
- cosmic curated COSV57557
- 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 -0.0609