EGFR c.1646T>C ;(p.F549S)

Variant ID: 7-55231440-T-C

NM_005228.3(EGFR):c.1646T>C;(p.F549S)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Analysis of single-nucleotide polymorphisms in genes associated with triple-negative breast cancer.

Frontiers In Genetics
G, Vigneshwaran V; Hasan, Qurratulain Annie QA; Kumar, Rahul R; Eranki, Avinash A
Publication Date: 2022

Variant appearance in text: rs1419611893
PubMed Link: 36561320
Variant Present in the following documents:
  • Table2.xlsx, sheet 4
View BVdb publication page



Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria.

American Journal Of Human Genetics
Pejaver, Vikas V; Byrne, Alicia B AB; Feng, Bing-Jian BJ; Pagel, Kymberleigh A KA; Mooney, Sean D SD; Karchin, Rachel R; O'Donnell-Luria, Anne A; Harrison, Steven M SM; Tavtigian, Sean V SV; Greenblatt, Marc S MS; Biesecker, Leslie G LG; Radivojac, Predrag P; Brenner, Steven E SE; ,
Publication Date: 2022-12-01

Variant appearance in text: EGFR: F549S; rs1419611893
PubMed Link: 36413997
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



Antibody neutralization of retargeted measles viruses.

Virology
Lech, Patrycja J PJ; Pappoe, Roland R; Nakamura, Takafumi T; Tobin, Gregory J GJ; Nara, Peter L PL; Russell, Stephen J SJ
Publication Date: 2014-04

Variant appearance in text: EGFR: F549S
PubMed Link: 24725950
Variant Present in the following documents:
  • Main text
View BVdb publication page