EGFR c.2326_2327insCTGCAC ;(p.C775_R776insPA)

Variant ID: 7-55249027-C-CCCTGCA

NM_005228.3(EGFR):c.2326_2327insCTGCAC;(p.C775_R776insPA)

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:

Dramatic reduction of sequence artefacts from DNA isolated from formalin-fixed cancer biopsies by treatment with uracil- DNA glycosylase.

Oncotarget
Do, Hongdo H; Dobrovic, Alexander A
Publication Date: 2012-05

Variant appearance in text: EGFR: C775_R776insPA
PubMed Link: 22643842
Variant Present in the following documents:
  • oncotarget-03-546.pdf
View BVdb publication page


High resolution melting analysis for rapid and sensitive EGFR and KRAS mutation detection in formalin fixed paraffin embedded biopsies.

Bmc Cancer
Do, Hongdo H; Krypuy, Michael M; Mitchell, Paul L PL; Fox, Stephen B SB; Dobrovic, Alexander A
Publication Date: 2008-05-21

Variant appearance in text: EGFR: C775_R776insPA
PubMed Link: 18495026
Variant Present in the following documents:
  • Main text
  • 1471-2407-8-142.pdf
View BVdb publication page