P9T (p.Pro9Thr) variant of NFE2L2 (Q16236)
P9T (p.Pro9Thr) in NFE2L2 (Q16236) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data.
P9T (p.Pro9Thr) variant details
- p.Pro9Thr
- gnomAD rs1281092624
- Missense
- Variant Prioritization Score for Impact Estimate 0.212
- REVEL 0.04
- CADD 20.00
- PolyPhen-2 0.03
- SIFT 1.00
- Most common in the East Asian population (allele frequency 3.2e-05)