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EGFR c.142_143delinsGC ;(p.F48A)
Variant ID: 7-55210032-TT-GC
NM_005228.3(
EGFR
):c.142_143delinsGC;(p.F48A)
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:
Core site-moiety maps reveal inhibitors and binding mechanisms of orthologous proteins by screening compound libraries.
Plos One
Hsu, Kai-Cheng KC; Cheng, Wen-Chi WC; Chen, Yen-Fu YF; Wang, Hung-Jung HJ; Li, Ling-Ting LT; Wang, Wen-Ching WC; Yang, Jinn-Moon JM
Publication Date: 2012
Variant appearance in text: EGFR: F48A
PubMed Link:
22393385
Variant Present in the following documents:
Main text
pone.0032142.pdf
View BVdb publication page