P16R (p.Pro16Arg) variant of TGM1 (P22735)
P16R (p.Pro16Arg) 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.
P16R (p.Pro16Arg) variant details
- p.Pro16Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available