T37P (p.Thr37Pro) variant of SRD5A2 (P31213)
T37P (p.Thr37Pro) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
T37P (p.Thr37Pro) variant details
- p.Thr37Pro
- ExAC rs782140524
- TOPMed rs782140524
- gnomAD rs782140524
- Missense
- Variant Prioritization Score for Impact Estimate 0.0866
- CADD 3.66
- PolyPhen-2 0.16
- SIFT 0.24
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available