EGFR c.2625+381C>G

Variant ID: 7-55259948-C-G

NM_005228.3(EGFR):c.2625+381C>G

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: rs17337331
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genetic variability in EGFR, Src and HER2 and risk of colorectal adenoma and cancer.

International Journal Of Molecular Epidemiology And Genetics
Poole, Elizabeth M EM; Curtin, Karen K; Hsu, Li L; Kulmacz, Richard J RJ; Duggan, David J DJ; Makar, Karen W KW; Xiao, Liren L; Carlson, Christopher S CS; Slattery, Martha L ML; Caan, Bette J BJ; Potter, John D JD; Ulrich, Cornelia M CM
Publication Date: 2011

Variant appearance in text: rs17337331
PubMed Link: 22199994
Variant Present in the following documents:
  • Main text
View BVdb publication page