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NF1 c.2660C>T ;(p.A887V)
Variant ID: 17-29556293-C-T
NM_001042492.2(
NF1
):c.2660C>T;(p.A887V)
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:
A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing.
Genome Medicine
Cao, Ye Y; Tokita, Mari J MJ; Chen, Edward S ES; Ghosh, Rajarshi R; Chen, Tiansheng T; Feng, Yanming Y; Gorman, Elizabeth E; Gibellini, Federica F; Ward, Patricia A PA; Braxton, Alicia A; Wang, Xia X; Meng, Linyan L; Xiao, Rui R; Bi, Weimin W; Xia, Fan F; Eng, Christine M CM; Yang, Yaping Y; Gambin, Tomasz T; Shaw, Chad C; Liu, Pengfei P; Stankiewicz, Pawel P
Publication Date: 2019-07-26
Variant appearance in text: NF1: 2660C>T
PubMed Link:
31349857
Variant Present in the following documents:
Main text
View BVdb publication page
Genomic Profiling on an Unselected Solid Tumor Population Reveals a Highly Mutated Wnt/β-Catenin Pathway Associated with Oncogenic EGFR Mutations.
Journal Of Personalized Medicine
Jiang, Jingrui J; Protopopov, Alexei A; Sun, Ruobai R; Lyle, Stephen S; Russell, Meaghan M
Publication Date: 2018-04-09
Variant appearance in text: NF1: A887V
PubMed Link:
29642553
Variant Present in the following documents:
Main text
jpm-08-00013.pdf
View BVdb publication page