EGFR c.1367T>C ;(p.I456T)

Variant ID: 7-55227900-T-C

NM_005228.3(EGFR):c.1367T>C;(p.I456T)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Analysis of single-nucleotide polymorphisms in genes associated with triple-negative breast cancer.

Frontiers In Genetics
G, Vigneshwaran V; Hasan, Qurratulain Annie QA; Kumar, Rahul R; Eranki, Avinash A
Publication Date: 2022

Variant appearance in text: EGFR: I456T
PubMed Link: 36561320
Variant Present in the following documents:
  • Table3.xlsx, sheet 1
  • Table2.xlsx, sheet 4
View BVdb publication page



ATR inhibitors as a synthetic lethal therapy for tumours deficient in ARID1A.

Nature Communications
Williamson, Chris T CT; Miller, Rowan R; Pemberton, Helen N HN; Jones, Samuel E SE; Campbell, James J; Konde, Asha A; Badham, Nicholas N; Rafiq, Rumana R; Brough, Rachel R; Gulati, Aditi A; Ryan, Colm J CJ; Francis, Jeff J; Vermulen, Peter B PB; Reynolds, Andrew R AR; Reaper, Philip M PM; Pollard, John R JR; Ashworth, Alan A; Lord, Christopher J CJ
Publication Date: 2016-12-13

Variant appearance in text: EGFR: I456T
PubMed Link: 27958275
Variant Present in the following documents:
  • ncomms13837-s4.xlsx, sheet 1
View BVdb publication page