V37G (p.Val37Gly) variant of CYP17A1 (P05093)
V37G (p.Val37Gly) in CYP17A1 (P05093) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data and structural context.
V37G (p.Val37Gly) variant details
- p.Val37Gly
- gnomAD rs1394909194
- Missense
- Variant Prioritization Score for Impact Estimate 0.658
- REVEL 0.74
- CADD 25.10
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available