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EGFR c.1681G>C ;(p.E561Q)
Variant ID: 7-55231475-G-C
NM_005228.3(
EGFR
):c.1681G>C;(p.E561Q)
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:
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: rs769918274
PubMed Link:
36561320
Variant Present in the following documents:
Table2.xlsx, sheet 4
View BVdb publication page