G38R (p.Gly38Arg) variant of MMADHC (Q9H3L0)
G38R (p.Gly38Arg) in MMADHC (Q9H3L0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G38R (p.Gly38Arg) variant details
- p.Gly38Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available