A113G (p.Ala113Gly) variant of CYP17A1 (P05093)
A113G (p.Ala113Gly) in CYP17A1 (P05093) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data and structural context.
A113G (p.Ala113Gly) variant details
- p.Ala113Gly
- gnomAD rs1297533084
- Missense
- Variant Prioritization Score for Impact Estimate 0.687
- REVEL 0.63
- CADD 25.10
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available