EGFR c.88+58324C>T

Variant ID: 7-55145382-C-T

NM_005228.3(EGFR):c.88+58324C>T

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: rs7809394
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Associations between EGFR gene polymorphisms and susceptibility to glioma: a systematic review and meta-analysis from GWAS and case-control studies.

Oncotarget
Yu, Xiao X; Sun, Nian Rong NR; Jang, Hai Tao HT; Guo, Shi Wen SW; Lian, Min Xue MX
Publication Date: 2017-10-17

Variant appearance in text: rs7809394
PubMed Link: 29156842
Variant Present in the following documents:
  • Main text
  • oncotarget-08-86877.pdf
View BVdb publication page