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EGFR c.89-41067C>T
Variant ID: 7-55168912-C-T
NM_005228.3(
EGFR
):c.89-41067C>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: rs4947974
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
A two-stage case-control study of EGFR polymorphisms and breast cancer risk.
Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Hong, Young-Seoub YS; Deming, Sandra L SL; Gao, Yu-Tang YT; Long, Ji-Rong JR; Shu, Xiao-Ou XO; Cai, Qiuyin Q; Lu, Wei W; Zheng, Wei W
Publication Date: 2009-02
Variant appearance in text: rs4947974
PubMed Link:
19190167
Variant Present in the following documents:
Main text
View BVdb publication page