P9A (p.Pro9Ala) variant of NFE2L2 (Q16236)
P9A (p.Pro9Ala) in NFE2L2 (Q16236) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data.
P9A (p.Pro9Ala) variant details
- p.Pro9Ala
- gnomAD rs1281092624
- Missense
- Variant Prioritization Score for Impact Estimate 0.222
- REVEL 0.06
- CADD 20.20
- PolyPhen-2 0.00
- SIFT 0.52
- Most common in the Non-Finnish European population (allele frequency 9.4e-07)