EGFR c.88+27258A>G

Variant ID: 7-55114316-A-G

NM_005228.3(EGFR):c.88+27258A>G

This variant was identified in 4 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: rs1015793
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: rs1015793
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: rs1015793
PubMed Link: 23236348
Variant Present in the following documents:
  • Main text
  • pone.0047929.pdf
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Inherited variation in immune genes and pathways and glioblastoma risk.

Carcinogenesis
Schwartzbaum, Judith A JA; Xiao, Yuanyuan Y; Liu, Yanhong Y; Tsavachidis, Spyros S; Berger, Mitchel S MS; Bondy, Melissa L ML; Chang, Jeffrey S JS; Chang, Susan M SM; Decker, Paul A PA; Ding, Bo B; Hepworth, Sarah J SJ; Houlston, Richard S RS; Hosking, Fay J FJ; Jenkins, Robert B RB; Kosel, Matthew L ML; McCoy, Lucie S LS; McKinney, Patricia A PA; Muir, Kenneth K; Patoka, Joe S JS; Prados, Michael M; Rice, Terri T; Robertson, Lindsay B LB; Schoemaker, Minouk J MJ; Shete, Sanjay S; Swerdlow, Anthony J AJ; Wiemels, Joe L JL; Wiencke, John K JK; Yang, Ping P; Wrensch, Margaret R MR
Publication Date: 2010-10

Variant appearance in text: rs1015793
PubMed Link: 20668009
Variant Present in the following documents:
  • Main text
  • bgq152.pdf
View BVdb publication page