EGFR c.2322_2323insCCACGT ;(p.V774_C775insPR)

Variant ID: 7-55249024-G-GCCACGT

NM_005228.3(EGFR):c.2322_2323insCCACGT;(p.V774_C775insPR)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genome-wide chemical mutagenesis screens allow unbiased saturation of the cancer genome and identification of drug resistance mutations.

Genome Research
Brammeld, Jonathan S JS; Petljak, Mia M; Martincorena, Inigo I; Williams, Steven P SP; Alonso, Luz Garcia LG; Dalmases, Alba A; Bellosillo, Beatriz B; Robles-Espinoza, Carla Daniela CD; Price, Stacey S; Barthorpe, Syd S; Tarpey, Patrick P; Alifrangis, Constantine C; Bignell, Graham G; Vidal, Joana J; Young, Jamie J; Stebbings, Lucy L; Beal, Kathryn K; Stratton, Michael R MR; Saez-Rodriguez, Julio J; Garnett, Mathew M; Montagut, Clara C; Iorio, Francesco F; McDermott, Ultan U
Publication Date: 2017-04

Variant appearance in text: EGFR: 2322_2323insCCACGT; V774_C775insPR
PubMed Link: 28179366
Variant Present in the following documents:
  • supp_gr.213546.116_Supplemental_Table_S7.xlsx, sheet 1
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: 2322_2323insCCACGT
PubMed Link: 18495026
Variant Present in the following documents:
  • Main text
  • 1471-2407-8-142.pdf
View BVdb publication page