S92F (p.Ser92Phe) variant of TGM1 (P22735)
S92F (p.Ser92Phe) 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.
S92F (p.Ser92Phe) variant details
- p.Ser92Phe
- NCI-TCGA Cosmic COSV5286
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available