TG c.1142dup ;(p.Y382Lfs*103)

Variant ID: 8-133898757-A-AG

NM_003235.4(TG):c.1142dup;(p.Y382Lfs*103)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Identification of potential modifier genes in Chinese patients with Wilson disease.

Metallomics : Integrated Biometal Science
Zhou, Donghu D; Jia, Siyu S; Yi, Liping L; Wu, Zhen Z; Song, Yi Y; Zhang, Bei B; Li, Yanmeng Y; Yang, Xiaoxi X; Xu, Anjian A; Li, Xiaojin X; Zhang, Wei W; Duan, Weijia W; Li, Zhenkun Z; Qi, Saiping S; Chen, Zhibin Z; Ouyang, Qin Q; Jia, Jidong J; Huang, Jian J; Ou, Xiaojuan X; You, Hong H
Publication Date: 2022-05-27

Variant appearance in text: TGN: 1141dupG
PubMed Link: 35357466
Variant Present in the following documents:
  • Main text
View BVdb publication page



Haplotype-resolved de novo assembly of the Vero cell line genome.

Npj Vaccines
Sène, Marie-Angélique MA; Kiesslich, Sascha S; Djambazian, Haig H; Ragoussis, Jiannis J; Xia, Yu Y; Kamen, Amine A AA
Publication Date: 2021-08-20

Variant appearance in text: TG: 1142dupG
PubMed Link: 34417462
Variant Present in the following documents:
  • 41541_2021_358_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page