THSD7A c.2506A>T ;(p.K836*)

Variant ID: 7-11500388-T-A

NM_015204.2(THSD7A):c.2506A>T;(p.K836*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Rare POLN mutations confer risk for familial nasopharyngeal carcinoma through weakened Epstein-Barr virus lytic replication.

Ebiomedicine
Xiao, Ruo-Wen RW; Wang, Fang F; Wang, Tong-Min TM; Zhang, Jiang-Bo JB; Wu, Zi-Yi ZY; Deng, Chang-Mi CM; Liao, Ying Y; Zhou, Ting T; Yang, Da-Wei DW; Dong, Si-Qi SQ; Xue, Wen-Qiong WQ; He, Yong-Qiao YQ; Zheng, Xiao-Hui XH; Li, Xi-Zhao XZ; Zhang, Pei-Fen PF; Zhang, Shao-Dan SD; Hu, Ye-Zhu YZ; Liu, Yu-Ying YY; Xia, Yun-Fei YF; Gao, Song S; Mu, Jian-Bing JB; Feng, Lin L; Jia, Wei-Hua WH
Publication Date: 2022-10

Variant appearance in text: THSD7A: K836X
PubMed Link: 36116213
Variant Present in the following documents:
  • mmc3.xlsx, sheet 3
View BVdb publication page