P26H (p.Pro26His) variant of IFNGR2 (Interferon gamma receptor 2)
P26H (p.Pro26His) in IFNGR2 (Interferon gamma receptor 2) 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.
P26H (p.Pro26His) variant details
- p.Pro26His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.19
- MetaSVM -0.93
- SIFT 0.19
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available