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CTTNBP2NL c.*531A>G
Variant ID: 1-113000565-A-G
NM_018704.2(
CTTNBP2NL
):c.*531A>G
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.
Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10
Variant appearance in text: rs3795821
PubMed Link:
29221171
Variant Present in the following documents:
oncotarget-08-95841-s002.xlsx, sheet 1
View BVdb publication page
Wnt signaling pathway pharmacogenetics in non-small cell lung cancer.
The Pharmacogenomics Journal
Stewart, D J DJ; Chang, D W DW; Ye, Y Y; Spitz, M M; Lu, C C; Shu, X X; Wampfler, J A JA; Marks, R S RS; Garces, Y I YI; Yang, P P; Wu, X X
Publication Date: 2014-12
Variant appearance in text: rs3795821
PubMed Link:
24980784
Variant Present in the following documents:
Main text
View BVdb publication page
miRNA-mediated relationships between Cis-SNP genotypes and transcript intensities in lymphocyte cell lines.
Plos One
Zhang, Wensheng W; Edwards, Andrea A; Zhu, Dongxiao D; Flemington, Erik K EK; Deininger, Prescott P; Zhang, Kun K
Publication Date: 2012
Variant appearance in text: rs3795821
PubMed Link:
22348086
Variant Present in the following documents:
Main text
pone.0031429.pdf
View BVdb publication page