EGFR c.2469+855A>G

Variant ID: 7-55250026-A-G

NM_005228.3(EGFR):c.2469+855A>G

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes.

Communications Biology
Perrino, Peter A PA; Talbot, Lidiya L; Kirkland, Rose R; Hill, Amanda A; Rendall, Amanda R AR; Mountford, Hayley S HS; Taylor, Jenny J; , ; Buscarello, Alexzandrea N AN; Lahiri, Nayana N; Saggar, Anand A; Fitch, R Holly RH; Newbury, Dianne F DF
Publication Date: 2020-04-20

Variant appearance in text: rs2075101
PubMed Link: 32313182
Variant Present in the following documents:
  • 42003_2020_885_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



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: rs2075101
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs2075101
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



Genetic association analysis of the RTK/ERK pathway with aggressive prostate cancer highlights the potential role of CCND2 in disease progression.

Scientific Reports
Chen, Yang Y; Zhang, Qin Q; Wang, Qiuyan Q; Li, Jie J; Sipeky, Csilla C; Xia, Jihan J; Gao, Ping P; Hu, Yanling Y; Zhang, Haiying H; Yang, Xiaobo X; Chen, Haitao H; Jiang, Yonghua Y; Yang, Yuehong Y; Yao, Ziting Z; Chen, Yinchun Y; Gao, Yong Y; Tan, Aihua A; Liao, Ming M; Schleutker, Johanna J; Xu, Jianfeng J; Sun, Yinghao Y; Wei, Gong-Hong GH; Mo, Zengnan Z
Publication Date: 2017-07-03

Variant appearance in text: rs2075101
PubMed Link: 28674394
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_4731.pdf
View BVdb publication page



Genetic variants of PTPN2 are associated with lung cancer risk: a re-analysis of eight GWASs in the TRICL-ILCCO consortium.

Scientific Reports
Feng, Yun Y; Wang, Yanru Y; Liu, Hongliang H; Liu, Zhensheng Z; Mills, Coleman C; Han, Younghun Y; Hung, Rayjean J RJ; Brhane, Yonathan Y; McLaughlin, John J; Brennan, Paul P; Bickeboeller, Heike H; Rosenberger, Albert A; Houlston, Richard S RS; Caporaso, Neil E NE; Teresa Landi, Maria M; Brueske, Irene I; Risch, Angela A; Ye, Yuanqing Y; Wu, Xifeng X; Christiani, David C DC; Amos, Christopher I CI; Wei, Qingyi Q
Publication Date: 2017-04-11

Variant appearance in text: rs2075101
PubMed Link: 28400551
Variant Present in the following documents:
View BVdb publication page



Association of Polymorphisms in Connective Tissue Growth Factor and Epidermal Growth Factor Receptor Genes With Human Longevity.

The Journals Of Gerontology. Series A, Biological Sciences And Medical Sciences
Donlon, Timothy A TA; Morris, Brian J BJ; He, Qimei Q; Chen, Randi R; Masaki, Kamal H KH; Allsopp, Richard C RC; Willcox, D Craig DC; Tranah, Gregory J GJ; Parimi, Neeta N; Evans, Daniel S DS; Flachsbart, Friederike F; Nebel, Almut A; Kim, Duk-Hwan DH; Park, Joobae J; Willcox, Bradley J BJ
Publication Date: 2017-08-01

Variant appearance in text: rs2075101
PubMed Link: 27365368
Variant Present in the following documents:
  • Main text
View BVdb publication page