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EGFR c.2890T>C ;(p.L964=)
Variant ID: 7-55268050-T-C
NM_005228.3(
EGFR
):c.2890T>C;(p.L964=)
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:
Impact and Diagnostic Gaps of Comprehensive Genomic Profiling in Real-World Clinical Practice.
Cancers
Singh, Aditi P AP; Shum, Elaine E; Rajdev, Lakshmi L; Cheng, Haiying H; Goel, Sanjay S; Perez-Soler, Roman R; Halmos, Balazs B
Publication Date: 2020-05-04
Variant appearance in text: EGFR: L964L
PubMed Link:
32375398
Variant Present in the following documents:
Main text
cancers-12-01156.pdf
View BVdb publication page
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: EGFR: L964L
PubMed Link:
28492226
Variant Present in the following documents:
ncomms15086-s3.xlsx, sheet 1
View BVdb publication page