G38D (p.Gly38Asp) variant of MMADHC (Q9H3L0)
G38D (p.Gly38Asp) in MMADHC (Q9H3L0) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G38D (p.Gly38Asp) variant details
- p.Gly38Asp
- TOPMed rs1386535158
- gnomAD rs1386535158
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available