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NF1 c.5969C>A ;(p.P1990Q)
Variant ID: 17-29662012-C-A
NM_001042492.2(
NF1
):c.5969C>A;(p.P1990Q)
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:
The Immunogenic Potential of Recurrent Cancer Drug Resistance Mutations: An In Silico Study.
Frontiers In Immunology
Punta, Marco M; Jennings, Victoria A VA; Melcher, Alan A AA; Lise, Stefano S
Publication Date: 2020
Variant appearance in text: NF1: P1990Q
PubMed Link:
33133066
Variant Present in the following documents:
Table_1.xlsx, sheet 2
Table_6.xlsx, sheet 7
Table_6.xlsx, sheet 2
View BVdb publication page
Diversity spectrum analysis identifies mutation-specific effects of cancer driver genes.
Communications Biology
Dong, Xiaobao X; Huang, Dandan D; Yi, Xianfu X; Zhang, Shijie S; Wang, Zhao Z; Yan, Bin B; Chung Sham, Pak P; Chen, Kexin K; Jun Li, Mulin M
Publication Date: 2020-01-07
Variant appearance in text: NF1: 5969C>A; P1990Q
PubMed Link:
31925297
Variant Present in the following documents:
42003_2019_736_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page