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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.
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: 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