T152R (p.Thr152Arg) variant of CYP17A1 (P05093)
T152R (p.Thr152Arg) in CYP17A1 (P05093) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
T152R (p.Thr152Arg) variant details
- p.Thr152Arg
- TOPMed rs58822002
- gnomAD rs58822002
- Missense
- Variant Prioritization Score for Impact Estimate 0.139
- REVEL 0.17
- CADD 5.56
- PolyPhen-2 0.36
- SIFT 0.20
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available