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EGFR c.2176G>T ;(p.V726L)
Variant ID: 7-55241728-G-T
NM_005228.3(
EGFR
):c.2176G>T;(p.V726L)
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:
Structural insights into drug development strategy targeting EGFR T790M/C797S.
Oncotarget
Zhu, Su-Jie SJ; Zhao, Peng P; Yang, Jiao J; Ma, Rui R; Yan, Xiao-E XE; Yang, Sheng-Yong SY; Yang, Jing-Wen JW; Yun, Cai-Hong CH
Publication Date: 2018-03-02
Variant appearance in text: EGFR: V726L
PubMed Link:
29568384
Variant Present in the following documents:
Main text
oncotarget-09-13652.pdf
View BVdb publication page
Significant Improvement in Detecting BRAF, KRAS, and EGFR Mutations Using Next-Generation Sequencing as Compared with FDA-Cleared Kits.
Molecular Diagnosis & Therapy
Ma, Wanlong W; Brodie, Steven S; Agersborg, Sally S; Funari, Vincent A VA; Albitar, Maher M
Publication Date: 2017-10
Variant appearance in text: EGFR: 2176G>T; Val726Leu
PubMed Link:
28639239
Variant Present in the following documents:
Main text
40291_2017_Article_290.pdf
View BVdb publication page