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EGFR c.861_862insCATGCA ;(p.F287_G288insHA)
Variant ID: 7-55221817-T-TCATGCA
NM_005228.3(
EGFR
):c.861_862insCATGCA;(p.F287_G288insHA)
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:
Case Report: Benefits of a NSCLC Patient With EGFR A289G/F287_G288insHA cis Mutations From Immunotherapy in Combination With Antiangiogenesis and Chemotherapy and Sequential Treatment of EGFR-TKI.
Frontiers In Oncology
Zhang, He H; Dong, Weiwei W; Zhao, Huixia H; Hu, Yanyan Y; You, Xia X; Sun, Tingting T; Xiao, Wenhua W
Publication Date: 2022
Variant appearance in text: EGFR: F287_G288insHA
PubMed Link:
35251994
Variant Present in the following documents:
Main text
fonc-12-826938.pdf
View BVdb publication page