V9M (p.Val9Met) variant of TGM1 (P22735)
V9M (p.Val9Met) 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.
V9M (p.Val9Met) variant details
- p.Val9Met
- Ensembl rs2040821278
- NCI-TCGA Cosmic COSV9925
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available