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EGFR c.2318_2319insACC ;(p.H773delinsQP)
Variant ID: 7-55249020-A-AACC
NM_005228.3(
EGFR
):c.2318_2319insACC;(p.H773delinsQP)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Next generation sequencing and molecular imaging identify EGFR mutation and amplification in a glioblastoma multiforme patient treated with an EGFR inhibitor: a case report.
Oncotarget
Zhou, Ke K; Yao, Hui H; Zhang, Xuewen X; Liu, Jiangang J; Qi, Zhenyu Z; Xie, Xueshun X; Xu, Xiaoting X; Zhou, Youxin Y; Yu, Zhengquan Z; Wang, Zhong Z; Che, Yanjun Y; Huang, Yulun Y
Publication Date: 2017-07-25
Variant appearance in text: EGFR: 2318_2319insACC
PubMed Link:
28611289
Variant Present in the following documents:
Main text
View BVdb publication page