S41R (p.Ser41Arg) variant of TPO (Thyroid peroxidase)
S41R (p.Ser41Arg) in TPO (Thyroid peroxidase) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Inborn genetic diseases.
S41R (p.Ser41Arg) variant details
- p.Ser41Arg
- 1000Genomes rs572043824
- ExAC rs572043824
- TOPMed rs572043824
- gnomAD rs572043824
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- EBI: Likely benign
- UniProt: Likely benign