EGFR c.931T>A ;(p.C311S)

Variant ID: 7-55223564-T-A

NM_005228.3(EGFR):c.931T>A;(p.C311S)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Association of Vascular Risk Factors and Genetic Factors With Penetrance of Variants Causing Monogenic Stroke.

Jama Neurology
Cho, Bernard P H BPH; Harshfield, Eric L EL; Al-Thani, Maha M; Tozer, Daniel J DJ; Bell, Steven S; Markus, Hugh S HS
Publication Date: 2022-10-27

Variant appearance in text: EGFR: 931T>A; Cys311Ser
PubMed Link: 36300346
Variant Present in the following documents:
  • jamaneurol-e223832-s001.pdf
View BVdb publication page



Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows.

Bmc Medical Genomics
Sobahy, Turki M TM; Tashkandi, Ghassan G; Bahussain, Donya D; Al-Harbi, Raneem R
Publication Date: 2022-04-25

Variant appearance in text: EGFR: 931T>A
PubMed Link: 35468810
Variant Present in the following documents:
  • 12920_2022_1235_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



CanDrA: cancer-specific driver missense mutation annotation with optimized features.

Plos One
Mao, Yong Y; Chen, Han H; Liang, Han H; Meric-Bernstam, Funda F; Mills, Gordon B GB; Chen, Ken K
Publication Date: 2013

Variant appearance in text: EGFR: C311S
PubMed Link: 24205039
Variant Present in the following documents:
  • pone.0077945.s001.xls, sheet 11
View BVdb publication page



Development of a fingerprinting panel using medically relevant polymorphisms.

Bmc Medical Genomics
Cross, Deanna S DS; Ivacic, Lynn C LC; McCarty, Catherine A CA
Publication Date: 2009-04-20

Variant appearance in text: EGFR: C311S
PubMed Link: 19379518
Variant Present in the following documents:
View BVdb publication page