G26R (p.Gly26Arg) variant of TPO (Thyroid peroxidase)
G26R (p.Gly26Arg) in TPO (Thyroid peroxidase) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes population frequency data.
G26R (p.Gly26Arg) variant details
- p.Gly26Arg
- cosmic curated COSV61111
- ExAC rs778914648
- TOPMed rs778914648
- gnomAD rs778914648
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Population evidence available