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EGFR c.89-55393G>C
Variant ID: 7-55154586-G-C
NM_005228.3(
EGFR
):c.89-55393G>C
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: rs12535578
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
RTK/ERK pathway under natural selection associated with prostate cancer.
Plos One
Chen, Yang Y; Xin, Xianxiang X; Li, Jie J; Xu, Jianfeng J; Yu, Xiaoxiang X; Li, Tianyu T; Mo, Zengnan Z; Hu, Yanling Y
Publication Date: 2013
Variant appearance in text: rs12535578
PubMed Link:
24223781
Variant Present in the following documents:
Main text
pone.0078254.pdf
View BVdb publication page
A Bayesian hierarchical model for analysis of SNP diversity in multilocus, multipopulation samples.
Journal Of The American Statistical Association
Guo, Feng F; Dey, Dipak K DK; Holsinger, Kent E KE
Publication Date: 2009-03-01
Variant appearance in text: rs12535578
PubMed Link:
19623271
Variant Present in the following documents:
Main text
View BVdb publication page