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EGFR c.2299_2301del ;(p.A767del)
Variant ID: 7-55249001-GGCC-G
NM_005228.3(
EGFR
):c.2299_2301del;(p.A767del)
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:
Successful treatment of a lung adenocarcinoma patient with a novel EGFR exon 20-ins mutation with afatinib: A case report.
Medicine
Cai, Yangyang Y; Wang, Xu X; Guo, Ye Y; Sun, Chao C; Xu, Yinghui Y; Qiu, Shi S; Ma, Kewei K
Publication Date: 2019-01
Variant appearance in text: EGFR: A767del
PubMed Link:
30608413
Variant Present in the following documents:
Main text
medi-98-e13890.pdf
View BVdb publication page
Impact of Concurrent Genomic Alterations Detected by Comprehensive Genomic Sequencing on Clinical Outcomes in East-Asian Patients with EGFR-Mutated Lung Adenocarcinoma.
Scientific Reports
Sato, Seijiro S; Nagahashi, Masayuki M; Koike, Terumoto T; Ichikawa, Hiroshi H; Shimada, Yoshifumi Y; Watanabe, Satoshi S; Kikuchi, Toshiaki T; Takada, Kazuki K; Nakanishi, Ryota R; Oki, Eiji E; Okamoto, Tatsuro T; Akazawa, Kouhei K; Lyle, Stephen S; Ling, Yiwei Y; Takabe, Kazuaki K; Okuda, Shujiro S; Wakai, Toshifumi T; Tsuchida, Masanori M
Publication Date: 2018-01-17
Variant appearance in text: EGFR: A767del
PubMed Link:
29343775
Variant Present in the following documents:
View BVdb publication page