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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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