EGFR c.1920-697G>A

Variant ID: 7-55239979-G-A

NM_005228.3(EGFR):c.1920-697G>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: rs2241054
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genetic effects and modifiers of radiotherapy and chemotherapy on survival in pancreatic cancer.

Pancreas
Zeng, Hongmei H; Yu, Herbert H; Lu, Lingeng L; Jain, Dhanpat D; Kidd, Mark S MS; Saif, M Wasif MW; Chanock, Stephen J SJ; Hartge, Patricia P; , ; Risch, Harvey A HA
Publication Date: 2011-07

Variant appearance in text: rs2241054
PubMed Link: 21487324
Variant Present in the following documents:
  • Main text
View BVdb publication page