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EGFR c.2119_2120delinsAG ;(p.L707R)
Variant ID: 7-55241671-TT-AG
NM_005228.3(
EGFR
):c.2119_2120delinsAG;(p.L707R)
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:
A homologous mapping method for three-dimensional reconstruction of protein networks reveals disease-associated mutations.
Bmc Systems Biology
Huang, Sing-Han SH; Lo, Yu-Shu YS; Luo, Yong-Chun YC; Tseng, Yu-Yao YY; Yang, Jinn-Moon JM
Publication Date: 2018-03-19
Variant appearance in text: EGFR: L707R
PubMed Link:
29560828
Variant Present in the following documents:
Main text
12918_2018_Article_537.pdf
View BVdb publication page