L9F (p.Leu9Phe) variant of RAG1 (P15918)
L9F (p.Leu9Phe) 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.
L9F (p.Leu9Phe) variant details
- p.Leu9Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available