Q77E (p.Gln77Glu) variant of CSF1R (P07333)
Q77E (p.Gln77Glu) in CSF1R (P07333) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Inborn genetic diseases.
Q77E (p.Gln77Glu) variant details
- p.Gln77Glu
- TOPMed rs1487923086
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance