Bibliome.ai browser hg19
Search
About
Stats
FAQ
EGFR c.89-46112G>A
Variant ID: 7-55163867-G-A
NM_005228.3(
EGFR
):c.89-46112G>A
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:
The Relationship between Metabolic Syndrome and Plasma Metals Modified by EGFR and TNF-α Gene Polymorphisms.
Toxics
Chen, Tzu-Hua TH; Kung, Wei-Shyang WS; Sun, Hung-Yu HY; Huang, Joh-Jong JJ; Lu, Jia-Yi JY; Luo, Kuei-Hau KH; Chuang, Hung-Yi HY
Publication Date: 2021-09-16
Variant appearance in text: rs3735061
PubMed Link:
34564376
Variant Present in the following documents:
Main text
toxics-09-00225.pdf
View BVdb publication page
Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.
The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04
Variant appearance in text: rs3735061
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page