P12R (p.Pro12Arg) variant of NFE2L2 (Q16236)
P12R (p.Pro12Arg) in NFE2L2 (Q16236) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data.
P12R (p.Pro12Arg) variant details
- p.Pro12Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.133
- REVEL 0.07
- CADD 19.40
- PolyPhen-2 0.04
- SIFT 0.48
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9.4e-07)