G89D (p.Gly89Asp) variant of FMR1 (Q06787)
G89D (p.Gly89Asp) in FMR1 (Q06787) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G89D (p.Gly89Asp) variant details
- p.Gly89Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available