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