M49V (p.Met49Val) variant of CYP17A1 (P05093)
M49V (p.Met49Val) 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.
M49V (p.Met49Val) variant details
- p.Met49Val
- Ensembl rs1844175113
- Missense
- Variant Prioritization Score for Impact Estimate 0.0863
- REVEL 0.09
- CADD 2.70
- PolyPhen-2 0.06
- SIFT 0.22
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available