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.




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