V97A (p.Val97Ala) variant of TGM1 (P22735)
V97A (p.Val97Ala) 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.
V97A (p.Val97Ala) variant details
- p.Val97Ala
- NCI-TCGA TCGA novel
- TOPMed rs2040816323
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available