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EGFR c.89-41786A>G
Variant ID: 7-55168193-A-G
NM_005228.3(
EGFR
):c.89-41786A>G
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Pharmacogenomics in drug-induced cardiotoxicity: Current status and the future.
Frontiers In Cardiovascular Medicine
Li, Mo-Yun MY; Peng, Li-Ming LM; Chen, Xiao-Ping XP
Publication Date: 2022
Variant appearance in text: rs142136033
PubMed Link:
36312261
Variant Present in the following documents:
Main text
fcvm-09-966261.pdf
View BVdb publication page
Genome-wide prioritization reveals novel gene signatures associated with cardiotoxic effects of tyrosine kinase inhibitors.
Oncology Letters
Li, Yilan Y; Wang, Weijie W; Gao, Rong R; Xu, Xueming X; Zhang, Yao Y
Publication Date: 2021-02
Variant appearance in text: rs142136033
PubMed Link:
33376527
Variant Present in the following documents:
Main text
ol-21-02-12355.pdf
View BVdb publication page