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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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