EGFR c.2654C>T ;(p.S885L)

Variant ID: 7-55260487-C-T

NM_005228.3(EGFR):c.2654C>T;(p.S885L)

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: S885L
PubMed Link: 36561320
Variant Present in the following documents:
  • Table3.xlsx, sheet 1
  • Table2.xlsx, sheet 4
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: EGFR: S885L; rs397517137
PubMed Link: 28492226
Variant Present in the following documents:
  • ncomms15086-s3.xlsx, sheet 1
View BVdb publication page



Detection of mutations in EGFR in circulating lung-cancer cells.

The New England Journal Of Medicine
Maheswaran, Shyamala S; Sequist, Lecia V LV; Nagrath, Sunitha S; Ulkus, Lindsey L; Brannigan, Brian B; Collura, Chey V CV; Inserra, Elizabeth E; Diederichs, Sven S; Iafrate, A John AJ; Bell, Daphne W DW; Digumarthy, Subba S; Muzikansky, Alona A; Irimia, Daniel D; Settleman, Jeffrey J; Tompkins, Ronald G RG; Lynch, Thomas J TJ; Toner, Mehmet M; Haber, Daniel A DA
Publication Date: 2008-07-24

Variant appearance in text: EGFR: S885L
PubMed Link: 18596266
Variant Present in the following documents:
  • Main text
View BVdb publication page