EGFR c.2502G>A ;(p.V834=)

Variant ID: 7-55259444-G-A

NM_005228.3(EGFR):c.2502G>A;(p.V834=)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Formalin fixation increases deamination mutation signature but should not lead to false positive mutations in clinical practice.

Plos One
Prentice, Leah M LM; Miller, Ruth R RR; Knaggs, Jeff J; Mazloomian, Alborz A; Aguirre Hernandez, Rosalia R; Franchini, Patrick P; Parsa, Kourosh K; Tessier-Cloutier, Basile B; Lapuk, Anna A; Huntsman, David D; Schaeffer, David F DF; Sheffield, Brandon S BS
Publication Date: 2018

Variant appearance in text: EGFR: V834V
PubMed Link: 29698444
Variant Present in the following documents:
  • pone.0196434.s001.xlsx, sheet 1
  • pone.0196434.s001.xlsx, sheet 3
  • pone.0196434.s001.xlsx, sheet 2
View BVdb publication page



Circulating tumour DNA sequence analysis as an alternative to multiple myeloma bone marrow aspirates.

Nature Communications
Kis, Olena O; Kaedbey, Rayan R; Chow, Signy S; Danesh, Arnavaz A; Dowar, Mark M; Li, Tiantian T; Li, Zhihua Z; Liu, Jessica J; Mansour, Mark M; Masih-Khan, Esther E; Zhang, Tong T; Bratman, Scott V SV; Oza, Amit M AM; Kamel-Reid, Suzanne S; Trudel, Suzanne S; Pugh, Trevor J TJ
Publication Date: 2017-05-11

Variant appearance in text: ERBB: 2502G>A
PubMed Link: 28492226
Variant Present in the following documents:
  • ncomms15086-s3.xlsx, sheet 1
View BVdb publication page



Frequency of mutations and polymorphisms in borderline ovarian tumors of known cancer genes.

Modern Pathology : An Official Journal Of The United States And Canadian Academy Of Pathology, Inc
Stemke-Hale, Katherine K; Shipman, Kristy K; Kitsou-Mylona, Isidora I; de Castro, David G DG; Hird, Vicky V; Brown, Robert R; Flanagan, James J; Gabra, Hani H; Mills, Gordon B GB; Agarwal, Roshan R; El-Bahrawy, Mona M
Publication Date: 2013-04

Variant appearance in text: EGFR: V834V
PubMed Link: 23174937
Variant Present in the following documents:
  • Main text
View BVdb publication page



Limited copy number-high resolution melting (LCN-HRM) enables the detection and identification by sequencing of low level mutations in cancer biopsies.

Molecular Cancer
Do, Hongdo H; Dobrovic, Alexander A
Publication Date: 2009-10-08

Variant appearance in text: EGFR: 2502G>A; V834V
PubMed Link: 19811662
Variant Present in the following documents:
  • Main text
  • 1476-4598-8-82.pdf
View BVdb publication page