Bibliome.ai browser hg19
Search
About
Stats
FAQ
SI c.83T>C ;(p.I28T)
Variant ID: 3-164793718-A-G
NM_001041.3(
SI
):c.83T>C;(p.I28T)
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:
Cancer related mutations in NRF2 impair its recognition by Keap1-Cul3 E3 ligase and promote malignancy.
Proceedings Of The National Academy Of Sciences Of The United States Of America
Shibata, Tatsuhiro T; Ohta, Tsutomu T; Tong, Kit I KI; Kokubu, Akiko A; Odogawa, Reiko R; Tsuta, Koji K; Asamura, Hisao H; Yamamoto, Masayuki M; Hirohashi, Setsuo S
Publication Date: 2008-09-09
Variant appearance in text: SI: I28T
PubMed Link:
18757741
Variant Present in the following documents:
Main text
View BVdb publication page