M156T (p.Met156Thr) variant of CYP17A1 (P05093)
M156T (p.Met156Thr) in CYP17A1 (P05093) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
M156T (p.Met156Thr) variant details
- p.Met156Thr
- ExAC rs774849280
- gnomAD rs774849280
- Missense
- Variant Prioritization Score for Impact Estimate 0.0992
- REVEL 0.11
- CADD 3.05
- PolyPhen-2 0.00
- SIFT 0.44
- Most common in the South Asian population (allele frequency 3.5e-05)
- Structural context available