C88W (p.Cys88Trp) variant of SRD5A2 (P31213)
C88W (p.Cys88Trp) in SRD5A2 (P31213) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes variant effect predictions and structural context.
C88W (p.Cys88Trp) variant details
- p.Cys88Trp
- TOPMed rs867198056
- Benign
- Missense
- SIFT 0.05
- EBI: Benign
- UniProt: Benign
- Structural context available