S37F (p.Ser37Phe) variant of RAG1 (P15918)
S37F (p.Ser37Phe) in RAG1 (P15918) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S37F (p.Ser37Phe) variant details
- p.Ser37Phe
- NCI-TCGA Cosmic COSV5502
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available