EGFR c.1798A>G ;(p.M600V)

Variant ID: 7-55233048-A-G

NM_005228.3(EGFR):c.1798A>G;(p.M600V)

This variant was identified in 3 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: M600V
PubMed Link: 36561320
Variant Present in the following documents:
  • Table2.xlsx, sheet 4
  • Table3.xlsx, sheet 1
View BVdb publication page



Detection and benchmarking of somatic mutations in cancer genomes using RNA-seq data.

Peerj
Coudray, Alexandre A; Battenhouse, Anna M AM; Bucher, Philipp P; Iyer, Vishwanath R VR
Publication Date: 2018

Variant appearance in text: EGFR: M600V
PubMed Link: 30083469
Variant Present in the following documents:
  • Main text
  • peerj-06-5362.pdf
View BVdb publication page



Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas.

Cell Reports
Way, Gregory P GP; Sanchez-Vega, Francisco F; La, Konnor K; Armenia, Joshua J; Chatila, Walid K WK; Luna, Augustin A; Sander, Chris C; Cherniack, Andrew D AD; Mina, Marco M; Ciriello, Giovanni G; Schultz, Nikolaus N; , ; Sanchez, Yolanda Y; Greene, Casey S CS
Publication Date: 2018-04-03

Variant appearance in text: EGFR: 1798A>G
PubMed Link: 29617658
Variant Present in the following documents:
  • NIHMS958974-supplement-6.xlsx, sheet 1
  • NIHMS958974-supplement-5.xlsx, sheet 1
View BVdb publication page