Bibliome.ai browser hg19
Search
About
Stats
FAQ
TG c.5735G>A ;(p.S1912N)
Variant ID: 8-133980087-G-A
NM_003235.4(
TG
):c.5735G>A;(p.S1912N)
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: 5735G>A
PubMed Link:
37087497
Variant Present in the following documents:
42003_2023_4784_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page
Mutation spectrum analysis of 29 causative genes in 43 Chinese patients with congenital hypothyroidism.
Molecular Medicine Reports
Wang, Huijuan H; Kong, Xiaohong X; Pei, Yanrui Y; Cui, Xuemei X; Zhu, Yijie Y; He, Zixuan Z; Wang, Yanxia Y; Zhang, Lirong L; Zhuo, Lixia L; Chen, Chao C; Yan, Xiaoli X
Publication Date: 2020-07
Variant appearance in text: TG: S1912N
PubMed Link:
32319661
Variant Present in the following documents:
Main text
mmr-22-01-0297.pdf
Supplementary_Data6.pdf
Supplementary_Data7.pdf
View BVdb publication page