Bibliome.ai browser hg19
Search
About
Stats
FAQ
EGFR c.88+58324C>T
Variant ID: 7-55145382-C-T
NM_005228.3(
EGFR
):c.88+58324C>T
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:
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: rs7809394
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Associations between EGFR gene polymorphisms and susceptibility to glioma: a systematic review and meta-analysis from GWAS and case-control studies.
Oncotarget
Yu, Xiao X; Sun, Nian Rong NR; Jang, Hai Tao HT; Guo, Shi Wen SW; Lian, Min Xue MX
Publication Date: 2017-10-17
Variant appearance in text: rs7809394
PubMed Link:
29156842
Variant Present in the following documents:
Main text
oncotarget-08-86877.pdf
View BVdb publication page