S74F (p.Ser74Phe) variant of SRD5A2 (P31213)
S74F (p.Ser74Phe) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
S74F (p.Ser74Phe) variant details
- p.Ser74Phe
- TOPMed rs1462234672
- gnomAD rs1462234672
- Missense
- Variant Prioritization Score for Impact Estimate 0.307
- CADD 14.50
- PolyPhen-2 0.01
- SIFT 0.06
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available