S74C (p.Ser74Cys) variant of SRD5A2 (P31213)
S74C (p.Ser74Cys) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
S74C (p.Ser74Cys) variant details
- p.Ser74Cys
- TOPMed rs1462234672
- gnomAD rs1462234672
- Missense
- Variant Prioritization Score for Impact Estimate 0.304
- CADD 14.10
- PolyPhen-2 0.02
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available