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TG c.2593C>A ;(p.P865T)
Variant ID: 8-133900645-C-A
NM_003235.4(
TG
):c.2593C>A;(p.P865T)
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: 2593C>A
PubMed Link:
37087497
Variant Present in the following documents:
42003_2023_4784_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page
Newborn Screening and Molecular Profile of Congenital Hypothyroidism in a Chinese Population.
Frontiers In Genetics
Yu, Bin B; Long, Wei W; Yang, Yuqi Y; Wang, Ying Y; Jiang, Lihua L; Cai, Zhengmao Z; Wang, Huaiyan H
Publication Date: 2018
Variant appearance in text: TG: 2593C>A; P865T
PubMed Link:
30420871
Variant Present in the following documents:
Main text
fgene-09-00509.pdf
View BVdb publication page