M99I (p.Met99Ile) variant of CYP17A1 (P05093)
M99I (p.Met99Ile) in CYP17A1 (P05093) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
M99I (p.Met99Ile) variant details
- p.Met99Ile
- cosmic curated COSV10468
- ExAC rs751850976
- TOPMed rs751850976
- gnomAD rs751850976
- Missense
- Variant Prioritization Score for Impact Estimate 0.304
- REVEL 0.14
- CADD 22.80
- PolyPhen-2 0.15
- SIFT 0.27
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Structural context available