D139H (p.Asp139His) variant of CYP17A1 (P05093)
D139H (p.Asp139His) in CYP17A1 (P05093) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
D139H (p.Asp139His) variant details
- p.Asp139His
- ExAC rs755526392
- TOPMed rs755526392
- gnomAD rs755526392
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available