EGFR c.88+10716A>G

Variant ID: 7-55097774-A-G

NM_005228.3(EGFR):c.88+10716A>G

This variant was identified in 2 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: rs28557040
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Germline polymorphisms in myeloid-associated genes are not associated with survival in glioma patients.

Journal Of Neuro-Oncology
Jacobs, Daniel I DI; Liu, Yanhong Y; Gabrusiewicz, Konrad K; Tsavachidis, Spiridon S; Armstrong, Georgina N GN; Zhou, Renke R; Wei, Jun J; Ivan, Cristina C; Calin, George G; Molinaro, Annette M AM; Rice, Terri T; Bracci, Paige M PM; Hansen, Helen M HM; Wiencke, John K JK; Wrensch, Margaret R MR; Heimberger, Amy B AB; Bondy, Melissa L ML
Publication Date: 2018-01

Variant appearance in text: rs28557040
PubMed Link: 28965162
Variant Present in the following documents:
  • Main text
View BVdb publication page