EGFR c.968T>C ;(p.V323A)

Variant ID: 7-55223601-T-C

NM_005228.3(EGFR):c.968T>C;(p.V323A)

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: rs367680488
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: V323A; rs367680488
PubMed Link: 36413997
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



Chemical genetic strategy for targeting protein kinases based on covalent complementarity.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Garske, Adam L AL; Peters, Ulf U; Cortesi, Arianna T AT; Perez, Jenny L JL; Shokat, Kevan M KM
Publication Date: 2011-09-13

Variant appearance in text: EGFR: V323A
PubMed Link: 21852571
Variant Present in the following documents:
  • Main text
View BVdb publication page