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EGFR c.89-12589C>T
Variant ID: 7-55197390-C-T
NM_005228.3(
EGFR
):c.89-12589C>T
This variant was identified in 3 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: rs11534100
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Intronic variant of EGFR is associated with GBAS expression and survival outcome of early-stage non-small cell lung cancer.
Thoracic Cancer
Hong, Mi Jeong MJ; Lee, Shin Yup SY; Choi, Jin Eun JE; Kang, Hyo-Gyoung HG; Do, Sook Kyung SK; Lee, Jang Hyuck JH; Yoo, Seung Soo SS; Lee, Eung Bae EB; Seok, Yangki Y; Cho, Sukki S; Jheon, Sanghoon S; Lee, Jaehee J; Cha, Seung Ick SI; Kim, Chang Ho CH; Park, Jae Yong JY
Publication Date: 2018-08
Variant appearance in text: rs11534100
PubMed Link:
29806744
Variant Present in the following documents:
Main text
TCA-9-916.pdf
View BVdb publication page
Adaptations to climate in candidate genes for common metabolic disorders.
Plos Genetics
Hancock, Angela M AM; Witonsky, David B DB; Gordon, Adam S AS; Eshel, Gidon G; Pritchard, Jonathan K JK; Coop, Graham G; Di Rienzo, Anna A
Publication Date: 2008-02
Variant appearance in text: rs11534100
PubMed Link:
18282109
Variant Present in the following documents:
pgen.0040032.pdf
View BVdb publication page