EGFR c.922_924delinsATG ;(p.V308M)

Variant ID: 7-55223555-GTC-ATG

NM_005228.3(EGFR):c.922_924delinsATG;(p.V308M)

This variant was identified in 1 publication

View GRCh38 version.



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

Publications:

Calibration-free NGS quantitation of mutations below 0.01% VAF.

Nature Communications
Dai, Peng P; Wu, Lucia Ruojia LR; Chen, Sherry Xi SX; Wang, Michael Xiangjiang MX; Cheng, Lauren Yuxuan LY; Zhang, Jinny Xuemeng JX; Hao, Pengying P; Yao, Weijie W; Zarka, Jabra J; Issa, Ghayas C GC; Kwong, Lawrence L; Zhang, David Yu DY
Publication Date: 2021-10-21

Variant appearance in text: EGFR: V308M
PubMed Link: 34675197
Variant Present in the following documents:
  • 41467_2021_Article_26308.pdf
View BVdb publication page