S17C (p.Ser17Cys) variant of CYP11B1 (P15538)
S17C (p.Ser17Cys) in CYP11B1 (P15538) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
S17C (p.Ser17Cys) variant details
- p.Ser17Cys
- 1000Genomes rs142591816
- ESP rs142591816
- ExAC rs142591816
- TOPMed rs142591816
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available