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.




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