P42H (p.Pro42His) variant of RAG1 (P15918)
P42H (p.Pro42His) in RAG1 (P15918) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
P42H (p.Pro42His) variant details
- p.Pro42His
- NCI-TCGA Cosmic COSV5502
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.56
- MetaSVM 0.14
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available