PC c.2098G>C ;(p.V700L)

Variant ID: 11-66618636-C-G

NM_001040716.1(PC):c.2098G>C;(p.V700L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome sequencing analysis identifies Epstein-Barr virus subtypes associated with high risk of nasopharyngeal carcinoma.

Nature Genetics
Xu, Miao M; Yao, Youyuan Y; Chen, Hui H; Zhang, Shanshan S; Cao, Su-Mei SM; Zhang, Zhe Z; Luo, Bing B; Liu, Zhiwei Z; Li, Zilin Z; Xiang, Tong T; He, Guiping G; Feng, Qi-Sheng QS; Chen, Li-Zhen LZ; Guo, Xiang X; Jia, Wei-Hua WH; Chen, Ming-Yuan MY; Zhang, Xiao X; Xie, Shang-Hang SH; Peng, Roujun R; Chang, Ellen T ET; Pedergnana, Vincent V; Feng, Lin L; Bei, Jin-Xin JX; Xu, Rui-Hua RH; Zeng, Mu-Sheng MS; Ye, Weimin W; Adami, Hans-Olov HO; Lin, Xihong X; Zhai, Weiwei W; Zeng, Yi-Xin YX; Liu, Jianjun J
Publication Date: 2019-07

Variant appearance in text: PC: V700L
PubMed Link: 31209392
Variant Present in the following documents:
  • Main text
  • nihms-1528858.pdf
  • NIHMS1528858-supplement-1.pdf
View BVdb publication page