EGFR c.2302_2303delinsTT ;(p.S768F)

Variant ID: 7-55249004-AG-TT

NM_005228.3(EGFR):c.2302_2303delinsTT;(p.S768F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A mutation-sensitive switch assay to detect five clinically significant epidermal growth factor receptor mutations.

Genetic Testing And Molecular Biomarkers
Liu, Bin B; Zhou, Lin L; Wang, Qian Q; Li, Kai K
Publication Date: 2015-06

Variant appearance in text: EGFR: S768F
PubMed Link: 25918867
Variant Present in the following documents:
  • Main text
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