Q98L (p.Gln98Leu) variant of CYP17A1 (P05093)
Q98L (p.Gln98Leu) in CYP17A1 (P05093) 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.
Q98L (p.Gln98Leu) variant details
- p.Gln98Leu
- ExAC rs757599828
- gnomAD rs757599828
- Missense
- Variant Prioritization Score for Impact Estimate 0.0886
- REVEL 0.08
- CADD 6.74
- PolyPhen-2 0.00
- SIFT 0.15
- Most common in the East Asian population (allele frequency 0.0001)
- Structural context available