VANGL1 c.464C>G ;(p.S155C)

Variant ID: 1-116206541-C-G

NM_138959.2(VANGL1):c.464C>G;(p.S155C)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Comprehensive genomic analysis of Oesophageal Squamous Cell Carcinoma reveals clinical relevance.

Scientific Reports
Du, Peina P; Huang, Peide P; Huang, Xuanlin X; Li, Xiangchun X; Feng, Zhimin Z; Li, Fengyu F; Liang, Shaoguang S; Song, Yongmei Y; Stenvang, Jan J; BrĂ¼nner, Nils N; Yang, Huanming H; Ou, Yunwei Y; Gao, Qiang Q; Li, Lin L
Publication Date: 2017-11-10

Variant appearance in text: VANGL1: 464C>G; S155C
PubMed Link: 29127303
Variant Present in the following documents:
  • 41598_2017_14909_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Genomic Characterization of Esophageal Squamous Cell Carcinoma Reveals Critical Genes Underlying Tumorigenesis and Poor Prognosis.

American Journal Of Human Genetics
Qin, Hai-De HD; Liao, Xiao-Yu XY; Chen, Yuan-Bin YB; Huang, Shao-Yi SY; Xue, Wen-Qiong WQ; Li, Fang-Fang FF; Ge, Xiao-Song XS; Liu, De-Qing DQ; Cai, Qiuyin Q; Long, Jirong J; Li, Xi-Zhao XZ; Hu, Ye-Zhu YZ; Zhang, Shao-Dan SD; Zhang, Lan-Jun LJ; Lehrman, Benjamin B; Scott, Alan F AF; Lin, Dongxin D; Zeng, Yi-Xin YX; Shugart, Yin Yao YY; Jia, Wei-Hua WH
Publication Date: 2016-04-07

Variant appearance in text: VANGL1: 464C>G; Ser155Cys
PubMed Link: 27058444
Variant Present in the following documents:
  • Main text
View BVdb publication page