NF1 c.3088_3089del ;(p.S1030Ifs*8)

Variant ID: 17-29557371-CCT-C

NM_001042492.2(NF1):c.3088_3089del;(p.S1030Ifs*8)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Discovery of targetable genetic alterations in advanced non-small cell lung cancer using a next-generation sequencing-based circulating tumor DNA assay.

Scientific Reports
Hou, Helei H; Yang, Xiaonan X; Zhang, Jinping J; Zhang, Zhe Z; Xu, Xiaomei X; Zhang, Xiaoping X; Zhang, Chuantao C; Liu, Dong D; Yan, Weihua W; Zhou, Na N; Zhu, Hongmei H; Qian, Zhaoyang Z; Li, Zhuokun Z; Zhang, Xiaochun X
Publication Date: 2017-11-06

Variant appearance in text: NF1: S1030Ifs*8
PubMed Link: 29097733
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_14962.pdf
View BVdb publication page



Clinical and Molecular Characterization of NF1 Patients: Single-Center Experience of 32 Patients From China.

Medicine
Zhu, Lude L; Zhang, Yunfeng Y; Tong, Hanxing H; Shao, Minhua M; Gu, Yong Y; Du, Xufeng X; Wang, Peiru P; Shi, Lei L; Zhang, Linglin L; Bi, Mingye M; Wang, Xiuli X; Zhang, Guolong G
Publication Date: 2016-03

Variant appearance in text: NF1: 3088_3089delTC
PubMed Link: 26962827
Variant Present in the following documents:
  • medi-95-e03043.pdf
View BVdb publication page