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EGFR c.478G>T ;(p.E160*)
Variant ID: 7-55214352-G-T
NM_005228.3(
EGFR
):c.478G>T;(p.E160*)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Circulating tumour DNA sequence analysis as an alternative to multiple myeloma bone marrow aspirates.
Nature Communications
Kis, Olena O; Kaedbey, Rayan R; Chow, Signy S; Danesh, Arnavaz A; Dowar, Mark M; Li, Tiantian T; Li, Zhihua Z; Liu, Jessica J; Mansour, Mark M; Masih-Khan, Esther E; Zhang, Tong T; Bratman, Scott V SV; Oza, Amit M AM; Kamel-Reid, Suzanne S; Trudel, Suzanne S; Pugh, Trevor J TJ
Publication Date: 2017-05-11
Variant appearance in text: ERBB: 478G>T
PubMed Link:
28492226
Variant Present in the following documents:
ncomms15086-s3.xlsx, sheet 1
View BVdb publication page
Targeting therapeutic liabilities engendered by PIK3R1 mutations for cancer treatment.
Pharmacogenomics
Cheung, Lydia Wt LW; Mills, Gordon B GB
Publication Date: 2016-02
Variant appearance in text: EGFR: E160*
PubMed Link:
26807692
Variant Present in the following documents:
Main text
View BVdb publication page