EGF c.1724+1398T>C

Variant ID: 4-110891673-T-C

NM_001963.4(EGF):c.1724+1398T>C

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: rs2298989
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genetic variations in EGF and EGFR and glioblastoma outcome.

Neuro-Oncology
Sjöström, Sara S; Andersson, Ulrika U; Liu, Yanhong Y; Brännström, Thomas T; Broholm, Helle H; Johansen, Christoffer C; Collatz-Laier, Helle H; Henriksson, Roger R; Bondy, Melissa M; Melin, Beatrice B
Publication Date: 2010-08

Variant appearance in text: rs2298989
PubMed Link: 20197289
Variant Present in the following documents:
  • Main text
  • noq018.pdf
View BVdb publication page