C6orf136 c.1106+47A>G

Variant ID: 6-30618906-A-G

NM_001161376.1(C6orf136):c.1106+47A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09

Variant appearance in text: rs9262135
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
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Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia.

Journal Of Psychiatry & Neuroscience : Jpn
Forstner, Andreas J AJ; Basmanav, F B FB; Mattheisen, Manuel M; Böhmer, Anne C AC; Hollegaard, Mads V MV; Janson, Esther E; Strengman, Eric E; Priebe, Lutz L; Degenhardt, Franziska F; Hoffmann, Per P; Herms, Stefan S; Maier, Wolfgang W; Mössner, Rainald R; Rujescu, Dan D; Ophoff, Roel A RA; Moebus, Susanne S; Mortensen, Preben B PB; Børglum, Anders D AD; Hougaard, David M DM; Frank, Josef J; Witt, Stephanie H SH; Rietschel, Marcella M; Zimmer, Andreas A; Nöthen, Markus M MM; Miró, Xavier X; Cichon, Sven S
Publication Date: 2014-11

Variant appearance in text: rs9262135
PubMed Link: 24936775
Variant Present in the following documents:
  • Main text
View BVdb publication page