EGFR c.88+60420G>A

Variant ID: 7-55147478-G-A

NM_005228.3(EGFR):c.88+60420G>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: rs10245472
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genetics in glioma: lessons learned from genome-wide association studies.

Current Opinion In Neurology
Melin, Beatrice B; Jenkins, Robert R
Publication Date: 2013-12

Variant appearance in text: rs10245472
PubMed Link: 24184969
Variant Present in the following documents:
  • Main text
View BVdb publication page



EGFR gene variants are associated with specific somatic aberrations in glioma.

Plos One
Wibom, Carl C; Ghasimi, Soma S; Van Loo, Peter P; Brännström, Thomas T; Trygg, Johan J; Lau, Ching C; Henriksson, Roger R; Bergenheim, Tommy T; Andersson, Ulrika U; Rydén, Patrik P; Melin, Beatrice B
Publication Date: 2012

Variant appearance in text: rs10245472
PubMed Link: 23236348
Variant Present in the following documents:
  • Main text
  • pone.0047929.pdf
View BVdb publication page