A13V (p.Ala13Val) variant of CYP17A1 (P05093)
A13V (p.Ala13Val) in CYP17A1 (P05093) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
A13V (p.Ala13Val) variant details
- p.Ala13Val
- gnomAD rs528612678
- Missense
- Variant Prioritization Score for Impact Estimate 0.13
- REVEL 0.03
- CADD 9.95
- PolyPhen-2 0.00
- SIFT 0.33
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available