EGFR c.976T>G ;(p.C326G)

Variant ID: 7-55223609-T-G

NM_005228.3(EGFR):c.976T>G;(p.C326G)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


appreci8: a pipeline for precise variant calling integrating 8 tools.

Bioinformatics (Oxford, England)
Sandmann, Sarah S; Karimi, Mohsen M; de Graaf, Aniek O AO; Rohde, Christian C; Göllner, Stefanie S; Varghese, Julian J; Ernsting, Jan J; Walldin, Gunilla G; van der Reijden, Bert A BA; Müller-Tidow, Carsten C; Malcovati, Luca L; Hellström-Lindberg, Eva E; Jansen, Joop H JH; Dugas, Martin M
Publication Date: 2018-12-15

Variant appearance in text: EGFR: 976T>G; Cys326Gly
PubMed Link: 29945233
Variant Present in the following documents:
  • bty518_supplementary_data_s8.xls, sheet 8
View BVdb publication page



Mutation-Structure-Function Relationship Based Integrated Strategy Reveals the Potential Impact of Deleterious Missense Mutations in Autophagy Related Proteins on Hepatocellular Carcinoma (HCC): A Comprehensive Informatics Approach.

International Journal Of Molecular Sciences
Awan, Faryal Mehwish FM; Obaid, Ayesha A; Ikram, Aqsa A; Janjua, Hussnain Ahmed HA
Publication Date: 2017-01-11

Variant appearance in text: EGFR: C326G
PubMed Link: 28085066
Variant Present in the following documents:
  • Main text
  • ijms-18-00139.pdf
View BVdb publication page