M11T (p.Met11Thr) variant of CYP11B1 (P15538)
M11T (p.Met11Thr) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
M11T (p.Met11Thr) variant details
- p.Met11Thr
- TOPMed rs1817089502
- gnomAD rs1817089502
- Missense
- Variant Prioritization Score for Impact Estimate 0.114
- REVEL 0.16
- CADD 0.31
- PolyPhen-2 0.00
- SIFT 0.19
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available