GC c.1352A>C ;(p.N451T)

Variant ID: 4-72618278-T-G

NM_000583.3(GC):c.1352A>C;(p.N451T)

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: GC: 1352A>C
PubMed Link: 37087497
Variant Present in the following documents:
  • 42003_2023_4784_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome.

Bmc Pediatrics
Gailite, Linda L; Rots, Dmitrijs D; Pukite, Ieva I; Cernevska, Gunta G; Kreile, Madara M
Publication Date: 2018-10-03

Variant appearance in text: GC: 1352A>C
PubMed Link: 30285761
Variant Present in the following documents:
  • Main text
  • 12887_2018_Article_1285.pdf
View BVdb publication page