R26T (p.Arg26Thr) variant of AMH (Anti-Muellerian hormone)
R26T (p.Arg26Thr) in AMH (Anti-Muellerian hormone) 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 structural context.
R26T (p.Arg26Thr) variant details
- p.Arg26Thr
- ExAC rs764149385
- TOPMed rs764149385
- gnomAD rs764149385
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available