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EGFR c.2314_2315insACA ;(p.P772delinsHT)
Variant ID: 7-55249016-C-CACA
NM_005228.3(
EGFR
):c.2314_2315insACA;(p.P772delinsHT)
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:
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: 2314_2315insACA; Pro772delinsHisThr
PubMed Link:
28639239
Variant Present in the following documents:
Main text
40291_2017_Article_290.pdf
View BVdb publication page