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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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