EGFR c.722_723inv ;(p.T241M)

Variant ID: 7-55220332-CA-TG

NM_005228.3(EGFR):c.722_723inv;(p.T241M)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Sequencing technology status of BRCA1/2 testing in Latin American Countries.

Npj Genomic Medicine
Solano, Angela R AR; Palmero, Edenir I EI; Delgado, Lucía L; Carraro, Dirce M DM; Ortíz-López, Rocío R; Carranza, Claudia L CL; Santamaria, Carlos C; Cifuentes, Laura L; Jara Sosa, Lilian E LE; Toland, Amanda E AE
Publication Date: 2020

Variant appearance in text: EGFR: T241M
PubMed Link: 32550004
Variant Present in the following documents:
  • 41525_2020_126_MOESM1_ESM.pdf
View BVdb publication page



Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics.

Scientific Reports
John, Sumi Elsa SE; Antony, Dinu D; Eaaswarkhanth, Muthukrishnan M; Hebbar, Prashantha P; Channanath, Arshad Mohamed AM; Thomas, Daisy D; Devarajan, Sriraman S; Tuomilehto, Jaakko J; Al-Mulla, Fahd F; Alsmadi, Osama O; Thanaraj, Thangavel Alphonse TA
Publication Date: 2018-11-08

Variant appearance in text: EGFR: Thr241Met
PubMed Link: 30409984
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_34815.pdf
View BVdb publication page



Inherited predisposition to glioma.

Neuro-Oncology
Kyritsis, Athanassios P AP; Bondy, Melissa L ML; Rao, Jasti S JS; Sioka, Chrissa C
Publication Date: 2010-01

Variant appearance in text: EGFR: Thr241Met
PubMed Link: 20150373
Variant Present in the following documents:
  • Main text
View BVdb publication page