E87Q (p.Glu87Gln) variant of RAG2 (P55895)
E87Q (p.Glu87Gln) 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.
E87Q (p.Glu87Gln) variant details
- p.Glu87Gln
- NCI-TCGA Cosmic COSV5755
- cosmic curated COSV57559
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available