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TG c.2000C>G ;(p.A667G)
Variant ID: 8-133899617-C-G
NM_003235.4(
TG
):c.2000C>G;(p.A667G)
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:
HaploCoV: unsupervised classification and rapid detection of novel emerging variants of SARS-CoV-2.
Communications Biology
Chiara, Matteo M; Horner, David S DS; Ferrandi, Erika E; Gissi, Carmela C; Pesole, Graziano G
Publication Date: 2023-04-22
Variant appearance in text: TG: 2000C>G; A667G
PubMed Link:
37087497
Variant Present in the following documents:
42003_2023_4784_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page
Recent Advances in the Targeting of Epigenetic Regulators in B-Cell Non-Hodgkin Lymphoma.
Frontiers In Genetics
Ribeiro, Marcelo L ML; Reyes-Garau, Diana D; Armengol, Marc M; Fernández-Serrano, Miranda M; Roué, Gaël G
Publication Date: 2019
Variant appearance in text: TG: A667G
PubMed Link:
31681423
Variant Present in the following documents:
Main text
fgene-10-00986.pdf
View BVdb publication page