R79I (p.Arg79Ile) variant of TGM1 (P22735)
R79I (p.Arg79Ile) in TGM1 (P22735) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R79I (p.Arg79Ile) variant details
- p.Arg79Ile
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available