EGFR c.2701+808A>C

Variant ID: 7-55261342-A-C

NM_005228.3(EGFR):c.2701+808A>C

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Anti-Irritant Strategy against Retinol Based on the Genetic Analysis of Korean Population: A Genetically Guided Top-Down Approach.

Pharmaceutics
Kang, Seongsu S; Kim, Kyunghoe K; Jun, Seung-Hyun SH; Lee, Seonju S; Kim, Juhyun J; Shin, Joong-Gon JG; Kim, Yunkwan Y; Kim, Mina M; Park, Sun-Gyoo SG; Kang, Nae-Gyu NG
Publication Date: 2021-11-25

Variant appearance in text: rs2740762
PubMed Link: 34959288
Variant Present in the following documents:
  • Main text
  • pharmaceutics-13-02006.pdf
View BVdb publication page



Anti-Irritant Strategy against Retinol Based on the Genetic Analysis of Korean Population: A Genetically Guided Top-Down Approach.

Pharmaceutics
Kang, Seongsu S; Kim, Kyunghoe K; Jun, Seung-Hyun SH; Lee, Seonju S; Kim, Juhyun J; Shin, Joong-Gon JG; Kim, Yunkwan Y; Kim, Mina M; Park, Sun-Gyoo SG; Kang, Nae-Gyu NG
Publication Date: 2021-11-25

Variant appearance in text: rs2740762
PubMed Link: 34959288
Variant Present in the following documents:
  • Main text
  • pharmaceutics-13-02006.pdf
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: rs2740762
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Epiregulin and EGFR interactions are involved in pain processing.

The Journal Of Clinical Investigation
Martin, Loren J LJ; Smith, Shad B SB; Khoutorsky, Arkady A; Magnussen, Claire A CA; Samoshkin, Alexander A; Sorge, Robert E RE; Cho, Chulmin C; Yosefpour, Noosha N; Sivaselvachandran, Sivaani S; Tohyama, Sarasa S; Cole, Tiffany T; Khuong, Thang M TM; Mir, Ellen E; Gibson, Dustin G DG; Wieskopf, Jeffrey S JS; Sotocinal, Susana G SG; Austin, Jean Sebastien JS; Meloto, Carolina B CB; Gitt, Joseph H JH; Gkogkas, Christos C; Sonenberg, Nahum N; Greenspan, Joel D JD; Fillingim, Roger B RB; Ohrbach, Richard R; Slade, Gary D GD; Knott, Charles C; Dubner, Ronald R; Nackley, Andrea G AG; Ribeiro-da-Silva, Alfredo A; Neely, G Gregory GG; Maixner, William W; Zaykin, Dmitri V DV; Mogil, Jeffrey S JS; Diatchenko, Luda L
Publication Date: 2017-09-01

Variant appearance in text: rs2740762
PubMed Link: 28783046
Variant Present in the following documents:
  • Main text
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: rs2740762
PubMed Link: 28400551
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_850.pdf
View BVdb publication page