EGFR c.88+58276G>A

Variant ID: 7-55145334-G-A

NM_005228.3(EGFR):c.88+58276G>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: rs9642564
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page


RTK/ERK pathway under natural selection associated with prostate cancer.

Plos One
Chen, Yang Y; Xin, Xianxiang X; Li, Jie J; Xu, Jianfeng J; Yu, Xiaoxiang X; Li, Tianyu T; Mo, Zengnan Z; Hu, Yanling Y
Publication Date: 2013

Variant appearance in text: rs9642564
PubMed Link: 24223781
Variant Present in the following documents:
  • Main text
  • pone.0078254.pdf
View BVdb publication page