TG c.2183C>A ;(p.T728K)

Variant ID: 8-133900235-C-A

NM_003235.4(TG):c.2183C>A;(p.T728K)

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: 2183C>A
PubMed Link: 37087497
Variant Present in the following documents:
  • 42003_2023_4784_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes.

European Journal Of Endocrinology
Sun, Feng F; Zhang, Jun-Xiu JX; Yang, Chang-Yi CY; Gao, Guan-Qi GQ; Zhu, Wen-Bin WB; Han, Bing B; Zhang, Le-Le LL; Wan, Yue-Yue YY; Ye, Xiao-Ping XP; Ma, Yu-Ru YR; Zhang, Man-Man MM; Yang, Liu L; Zhang, Qian-Yue QY; Liu, Wei W; Guo, Cui-Cui CC; Chen, Gang G; Zhao, Shuang-Xia SX; Song, Ke-Yi KY; Song, Huai-Dong HD
Publication Date: 2018-06

Variant appearance in text: TG: T728K
PubMed Link: 29650690
Variant Present in the following documents:
  • Main text
  • eje-178-623-t001.pdf
  • eje-178-623.pdf
View BVdb publication page