EGFR c.145C>T ;(p.L49F)

Variant ID: 7-55210035-C-T

NM_005228.3(EGFR):c.145C>T;(p.L49F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Exome Sequencing Identifies Potentially Druggable Mutations in Nasopharyngeal Carcinoma.

Scientific Reports
Chow, Yock Ping YP; Tan, Lu Ping LP; Chai, San Jiun SJ; Abdul Aziz, Norazlin N; Choo, Siew Woh SW; Lim, Paul Vey Hong PV; Pathmanathan, Rajadurai R; Mohd Kornain, Noor Kaslina NK; Lum, Chee Lun CL; Pua, Kin Choo KC; Yap, Yoke Yeow YY; Tan, Tee Yong TY; Teo, Soo Hwang SH; Khoo, Alan Soo-Beng AS; Patel, Vyomesh V
Publication Date: 2017-03-03

Variant appearance in text: EGFR: L49F
PubMed Link: 28256603
Variant Present in the following documents:
  • Main text
  • srep42980.pdf
  • srep42980-s2.xls, sheet 9
View BVdb publication page