EGFR c.1627G>T ;(p.E543*)

Variant ID: 7-55229320-G-T

NM_005228.3(EGFR):c.1627G>T;(p.E543*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: 1627G>T
PubMed Link: 28492226
Variant Present in the following documents:
  • ncomms15086-s3.xlsx, sheet 1
View BVdb publication page



Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens.

The Journal Of Molecular Diagnostics : Jmd
Pritchard, Colin C CC; Salipante, Stephen J SJ; Koehler, Karen K; Smith, Christina C; Scroggins, Sheena S; Wood, Brent B; Wu, David D; Lee, Ming K MK; Dintzis, Suzanne S; Adey, Andrew A; Liu, Yajuan Y; Eaton, Keith D KD; Martins, Renato R; Stricker, Kari K; Margolin, Kim A KA; Hoffman, Noah N; Churpek, Jane E JE; Tait, Jonathan F JF; King, Mary-Claire MC; Walsh, Tom T
Publication Date: 2014-01

Variant appearance in text: EGFR: 1627G>T
PubMed Link: 24189654
Variant Present in the following documents:
  • Main text
View BVdb publication page