EGFR c.89-7381G>A

Variant ID: 7-55202598-G-A

NM_005228.3(EGFR):c.89-7381G>A

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: rs17172446
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



SNP-SNP interaction network in angiogenesis genes associated with prostate cancer aggressiveness.

Plos One
Lin, Hui-Yi HY; Amankwah, Ernest K EK; Tseng, Tung-Sung TS; Qu, Xiaotao X; Chen, Dung-Tsa DT; Park, Jong Y JY
Publication Date: 2013

Variant appearance in text: rs17172446
PubMed Link: 23593148
Variant Present in the following documents:
  • Main text
  • pone.0059688.pdf
View BVdb publication page



Next-generation analysis of cataracts: determining knowledge driven gene-gene interactions using Biofilter, and gene-environment interactions using the PhenX Toolkit.

Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing
Pendergrass, Sarah A SA; Verma, Shefali S SS; Holzinger, Emily R ER; Moore, Carrie B CB; Wallace, John J; Dudek, Scott M SM; Huggins, Wayne W; Kitchner, Terrie T; Waudby, Carol C; Berg, Richard R; McCarty, Catherine A CA; Ritchie, Marylyn D MD
Publication Date: 2013

Variant appearance in text: rs17172446
PubMed Link: 23424120
Variant Present in the following documents:
  • Main text
View BVdb publication page