EGFR c.2469+959G>A

Variant ID: 7-55250130-G-A

NM_005228.3(EGFR):c.2469+959G>A

This variant was identified in 7 publications

View GRCh38 version.




Publications:


The effect of SNPs in lncRNA as ceRNA on the risk and prognosis of hepatocellular carcinoma.

Bmc Genomics
Mo, Han H; Wang, Xi X; Ji, Guohua G; Liang, Xiao X; Yang, Yi Y; Sun, Wenjing W; Jia, Xueyuan X; Xu, Lidan L; Qiao, Yuandong Y; Zhou, Henan H; Zhao, Wenhui W; Fu, Songbin S; Zhang, Xuelong X
Publication Date: 2022-11-24

Variant appearance in text: rs7795743
PubMed Link: 36418931
Variant Present in the following documents:
  • Main text
  • 12864_2022_Article_9010.pdf
View BVdb publication page



Mutational landscape of gastric adenocarcinoma in Latin America: A genetic approach for precision medicine.

Genes & Diseases
Cerrato-Izaguirre, Dennis D; Chirino, Yolanda I YI; García-Cuellar, Claudia M CM; Santibáñez-Andrade, Miguel M; Prada, Diddier D; Hernández-Guerrero, Angélica A; Larraga, Octavio Alonso OA; Camacho, Javier J; Sánchez-Pérez, Yesennia Y
Publication Date: 2022-07

Variant appearance in text: rs7795743
PubMed Link: 35685475
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



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: rs7795743
PubMed Link: 32313182
Variant Present in the following documents:
  • 42003_2020_885_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



GOG 8020/210: Risk stratification of lymph node metastasis, disease progression and survival using single nucleotide polymorphisms in endometrial cancer: An NRG oncology/gynecologic oncology group study.

Gynecologic Oncology
Brooks, Rebecca A RA; Tritchler, David S DS; Darcy, Kathleen M KM; Lankes, Heather A HA; Salani, Ritu R; Sperduto, Paul P; Guntupalli, Saketh S; DiSilvestro, Paul P; Kesterson, Joshua J; Olawaiye, Alexander B AB; Moxley, Katherine K; Waggoner, Steven S; Santin, Alessandro A; Rader, Janet S JS; Kizer, Nora T NT; Thaker, Premal H PH; Powell, Matthew A MA; Mutch, David G DG; Birrer, Michael J MJ; Goodfellow, Paul J PJ
Publication Date: 2019-05

Variant appearance in text: rs7795743
PubMed Link: 30827726
Variant Present in the following documents:
  • Main text
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: rs7795743
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: rs7795743
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
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: rs7795743
PubMed Link: 27365368
Variant Present in the following documents:
  • Main text
View BVdb publication page