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EGFR c.2302_2303delinsTT ;(p.S768F)
Variant ID: 7-55249004-AG-TT
NM_005228.3(
EGFR
):c.2302_2303delinsTT;(p.S768F)
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:
A mutation-sensitive switch assay to detect five clinically significant epidermal growth factor receptor mutations.
Genetic Testing And Molecular Biomarkers
Liu, Bin B; Zhou, Lin L; Wang, Qian Q; Li, Kai K
Publication Date: 2015-06
Variant appearance in text: EGFR: S768F
PubMed Link:
25918867
Variant Present in the following documents:
Main text
View BVdb publication page