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NUP214 c.1475C>G ;(p.S492C)
Variant ID: 9-134019847-C-G
NM_005085.3(
NUP214
):c.1475C>G;(p.S492C)
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:
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: NUP214: S492C
PubMed Link:
29642553
Variant Present in the following documents:
Main text
jpm-08-00013.pdf
View BVdb publication page
The chronological sequence of somatic mutations in early gastric carcinogenesis inferred from multiregion sequencing of gastric adenomas.
Oncotarget
Lim, Chul-Hyun CH; Cho, Yu Kyung YK; Kim, Sang Woo SW; Choi, Myung-Gyu MG; Rhee, Je-Keun JK; Chung, Yeun-Jun YJ; Lee, Sug-Hyung SH; Kim, Tae-Min TM
Publication Date: 2016-06-28
Variant appearance in text: NUP214: S492C
PubMed Link:
27175599
Variant Present in the following documents:
oncotarget-07-39758-s006.xlsx, sheet 1
View BVdb publication page