EGFR c.2283+2225C>T

Variant ID: 7-55244738-C-T

NM_005228.3(EGFR):c.2283+2225C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics.

International Journal Of Cancer
Ostrom, Quinn T QT; Egan, Kathleen M KM; Nabors, L Burt LB; Gerke, Travis T; Thompson, Reid C RC; Olson, Jeffrey J JJ; LaRocca, Renato R; Chowdhary, Sajeel S; Eckel-Passow, Jeanette E JE; Armstrong, Georgina G; Wiencke, John K JK; Bernstein, Jonine L JL; Claus, Elizabeth B EB; Il'yasova, Dora D; Johansen, Christoffer C; Lachance, Daniel H DH; Lai, Rose K RK; Merrell, Ryan T RT; Olson, Sara H SH; Sadetzki, Siegal S; Schildkraut, Joellen M JM; Shete, Sanjay S; Houlston, Richard S RS; Jenkins, Robert B RB; Wrensch, Margaret R MR; Melin, Beatrice B; Amos, Christopher I CI; Huse, Jason T JT; Barnholtz-Sloan, Jill S JS; Bondy, Melissa L ML
Publication Date: 2020-02-01

Variant appearance in text: rs56129111
PubMed Link: 30963577
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: rs56129111
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page