IQSEC3 c.517_528del ;(p.S173_G176del)

Variant ID: 12-176563-CCTCCGCCCTCGG-C

NM_001170738.1(IQSEC3):c.517_528del;(p.S173_G176del)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of recurrent USP48 and BRAF mutations in Cushing's disease.

Nature Communications
Chen, Jianhua J; Jian, Xuemin X; Deng, Siyu S; Ma, Zengyi Z; Shou, Xuefei X; Shen, Yue Y; Zhang, Qilin Q; Song, Zhijian Z; Li, Zhiqiang Z; Peng, Hong H; Peng, Cheng C; Chen, Min M; Luo, Cheng C; Zhao, Dan D; Ye, Zhao Z; Shen, Ming M; Zhang, Yichao Y; Zhou, Juan J; Fahira, Aamir A; Wang, Yongfei Y; Li, Shiqi S; Zhang, Zhaoyun Z; Ye, Hongying H; Li, Yiming Y; Shen, Jiawei J; Chen, Hong H; Tang, Feng F; Yao, Zhenwei Z; Shi, Zhifeng Z; Chen, Chunjui C; Xie, Lu L; Wang, Ye Y; Fu, Chaowei C; Mao, Ying Y; Zhou, Liangfu L; Gao, Daming D; Yan, Hai H; Zhao, Yao Y; Huang, Chuanxin C; Shi, Yongyong Y
Publication Date: 2018-08-09

Variant appearance in text: IQSEC3: 516_527del
PubMed Link: 30093687
Variant Present in the following documents:
  • 41467_2018_5275_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page