M68V (p.Met68Val) variant of CYP17A1 (P05093)
M68V (p.Met68Val) in CYP17A1 (P05093) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
M68V (p.Met68Val) variant details
- p.Met68Val
- ExAC rs752052614
- gnomAD rs752052614
- Missense
- Variant Prioritization Score for Impact Estimate 0.169
- REVEL 0.25
- CADD 0.10
- PolyPhen-2 0.40
- SIFT 0.14
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available