I63T (p.Ile63Thr) variant of CYP17A1 (P05093)
I63T (p.Ile63Thr) in CYP17A1 (P05093) 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.
I63T (p.Ile63Thr) variant details
- p.Ile63Thr
- TOPMed rs1844174479
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available