R43P (p.Arg43Pro) variant of NFE2L2 (Q16236)
R43P (p.Arg43Pro) in NFE2L2 (Q16236) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
R43P (p.Arg43Pro) variant details
- p.Arg43Pro
- 1000Genomes rs35248500
- ESP rs35248500
- ExAC rs35248500
- TOPMed rs35248500
- Benign
- Missense
- EBI: Benign (in dbSNP:rs35248500)
- UniProt: Benign (in dbSNP:rs35248500)
- Structural context available