EGFR c.2236_2259del ;(p.E746_P753del)

Variant ID: 7-55242464-AGGAATTAAGAGAAGCAACATCTCC-A

NM_005228.3(EGFR):c.2236_2259del;(p.E746_P753del)

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:

Different subtypes of EGFR exon19 mutation can affect prognosis of patients with non-small cell lung adenocarcinoma.

Plos One
Tian, Yingying Y; Zhao, Jiuzhou J; Ren, Pengfei P; Wang, Bo B; Zhao, Chengzhi C; Shi, Chao C; Wei, Bing B; Ma, Jie J; Guo, Yongjun Y
Publication Date: 2018

Variant appearance in text: EGFR: Glu746_Pro753del
PubMed Link: 30383772
Variant Present in the following documents:
  • Main text
  • pone.0201682.pdf
View BVdb publication page


Diagnostic value of H3F3A mutations in giant cell tumour of bone compared to osteoclast-rich mimics.

The Journal Of Pathology. Clinical Research
Presneau, Nadège N; Baumhoer, Daniel D; Behjati, Sam S; Pillay, Nischalan N; Tarpey, Patrick P; Campbell, Peter J PJ; Jundt, Gernot G; Hamoudi, Rifat R; Wedge, David C DC; Loo, Peter Van PV; Hassan, A Bassim AB; Khatri, Bhavisha B; Ye, Hongtao H; Tirabosco, Roberto R; Amary, M Fernanda MF; Flanagan, Adrienne M AM
Publication Date: 2015-04

Variant appearance in text: EGFR: E746_P753del
PubMed Link: 27499898
Variant Present in the following documents:
  • CJP2-1-113-s004.xlsx, sheet 1
View BVdb publication page