EGFR c.89-6141G>A

Variant ID: 7-55203838-G-A

NM_005228.3(EGFR):c.89-6141G>A

This variant was identified in 2 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: rs6969570
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Identification of epidermal growth factor receptor (EGFR) genetic variants that modify risk for head and neck squamous cell carcinoma.

Cancer Letters
Fung, Christopher C; Zhou, Pei P; Joyce, Sonali S; Trent, Kerry K; Yuan, Jian-Min JM; Grandis, Jennifer R JR; Weissfeld, Joel L JL; Romkes, Marjorie M; Weeks, Daniel E DE; Egloff, Ann Marie AM
Publication Date: 2015-02-28

Variant appearance in text: rs6969570
PubMed Link: 25511740
Variant Present in the following documents:
  • Main text
View BVdb publication page