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EGFR c.88+29649G>A
Variant ID: 7-55116707-G-A
NM_005228.3(
EGFR
):c.88+29649G>A
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: rs759165
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Single nucleotide polymorphisms as susceptibility, prognostic, and therapeutic markers of nonsmall cell lung cancer.
Lung Cancer (Auckland, N.Z.)
Zienolddiny, Shanbeh S; Skaug, Vidar V
Publication Date: 2012
Variant appearance in text: rs759165
PubMed Link:
28210120
Variant Present in the following documents:
Main text
View BVdb publication page