R43G (p.Arg43Gly) variant of NFE2L2 (Q16236)
R43G (p.Arg43Gly) in NFE2L2 (Q16236) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
R43G (p.Arg43Gly) variant details
- p.Arg43Gly
- NCI-TCGA Cosmic COSV6796
- cosmic curated COSV67960
- 1000Genomes rs182428269
- ESP rs182428269
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance (in dbSNP:rs35248500)
- UniProt: Uncertain significance (in dbSNP:rs35248500)
- Structural context available