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EGFR c.2071C>A ;(p.P691T)
Variant ID: 7-55241623-C-A
NM_005228.3(
EGFR
):c.2071C>A;(p.P691T)
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:
Analysis of single-nucleotide polymorphisms in genes associated with triple-negative breast cancer.
Frontiers In Genetics
G, Vigneshwaran V; Hasan, Qurratulain Annie QA; Kumar, Rahul R; Eranki, Avinash A
Publication Date: 2022
Variant appearance in text: rs1168763004
PubMed Link:
36561320
Variant Present in the following documents:
Table2.xlsx, sheet 4
View BVdb publication page
Next-generation sequencing of lung cancer EGFR exons 18-21 allows effective molecular diagnosis of small routine samples (cytology and biopsy).
Plos One
de Biase, Dario D; Visani, Michela M; Malapelle, Umberto U; Simonato, Francesca F; Cesari, Valentina V; Bellevicine, Claudio C; Pession, Annalisa A; Troncone, Giancarlo G; Fassina, Ambrogio A; Tallini, Giovanni G
Publication Date: 2013
Variant appearance in text: EGFR: P691T
PubMed Link:
24376723
Variant Present in the following documents:
Main text
pone.0083607.pdf
View BVdb publication page