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.




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