EGFR c.55_57delinsATG ;(p.C19M)

Variant ID: 7-55087025-TGC-ATG

NM_005228.3(EGFR):c.55_57delinsATG;(p.C19M)

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:

Genetic Abnormalities, Clonal Evolution, and Cancer Stem Cells of Brain Tumors.

Medical Sciences (Basel, Switzerland)
Testa, Ugo U; Castelli, Germana G; Pelosi, Elvira E
Publication Date: 2018-10-02

Variant appearance in text: EGFR: C19M
PubMed Link: 30279357
Variant Present in the following documents:
  • Main text
  • medsci-06-00085.pdf
View BVdb publication page