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NF1 c.466C>T ;(p.R156C)
Variant ID: 17-29490381-C-T
NM_001042492.2(
NF1
):c.466C>T;(p.R156C)
This variant was identified in 4 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
An EGFR L858R mutation identified in 1862 Chinese NSCLC patients can be a promising neoantigen vaccine therapeutic strategy.
Frontiers In Immunology
Lin, Jing J; Liu, Jun J; Hao, Shi-Guang SG; Lan, Bin B; Zheng, Xiao-Bin XB; Xiong, Jia-Ni JN; Zhang, Ying-Qian YQ; Gao, Xuan X; Chen, Chuan-Ben CB; Chen, Ling L; Huang, Yu-Fang YF; Luo, Hong H; Yi, Yu-Ting YT; Yi, Xin X; Lu, Jian-Ping JP; Zheng, Xiong-Wei XW; Chen, Gang G; Wang, Xue-Feng XF; Chen, Yu Y
Publication Date: 2022
Variant appearance in text: NF1: 466C>T; R156C
PubMed Link:
36505399
Variant Present in the following documents:
Table_2.xlsx, sheet 3
Table_2.xlsx, sheet 2
View BVdb publication page
.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
Publication Date: 2017
Variant appearance in text: NF1: 466C>T; Arg156Cys
PubMed Link:
32214685
Variant Present in the following documents:
11825_2017_Article_126.pdf
View BVdb publication page
TAPES: A tool for assessment and prioritisation in exome studies.
Plos Computational Biology
Xavier, Alexandre A; Scott, Rodney J RJ; Talseth-Palmer, Bente A BA
Publication Date: 2019-10
Variant appearance in text: NF1: R156C; rs755890242
PubMed Link:
31613886
Variant Present in the following documents:
pcbi.1007453.s004.xlsx, sheet 2
pcbi.1007453.s002.xlsx, sheet 1
View BVdb publication page
Exhaustive non-synonymous variants functionality prediction enables high resolution characterization of the neurofibromin architecture.
Ebiomedicine
Isakov, Ofer O; Wallis, Deeann D; Evans, D Gareth DG; Ben-Shachar, Shay S
Publication Date: 2018-10
Variant appearance in text: rs755890242
PubMed Link:
30274822
Variant Present in the following documents:
mmc1.xls, sheet 1
View BVdb publication page