HR c.236A>G ;(p.E79G)

Variant ID: 8-21986448-T-C

NM_005144.4(HR):c.236A>G;(p.E79G)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Functional polymorphisms in Nrf2: implications for human disease.

Free Radical Biology & Medicine
Cho, Hye-Youn HY; Marzec, Jacqui J; Kleeberger, Steven R SR
Publication Date: 2015-11

Variant appearance in text: HR: 236A>G
PubMed Link: 26117318
Variant Present in the following documents:
  • Main text
View BVdb publication page