EGFR c.88+2905C>G

Variant ID: 7-55089963-C-G

NM_005228.3(EGFR):c.88+2905C>G

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: rs7787739
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page


Abstracts for the 15th International Congress on Schizophrenia Research (ICOSR), March 28-April 1, 2015, Colorado Springs, Colorado.

Schizophrenia Bulletin
Publication Date: 2015-03

Variant appearance in text: rs7787739
PubMed Link: 26305006
Variant Present in the following documents:
  • Main text
View BVdb publication page