TM7SF2 c.459G>C ;(p.Q153H)

Variant ID: 11-64880846-G-C

NM_003273.3(TM7SF2):c.459G>C;(p.Q153H)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing.

Genome Biology
Demeulemeester, Jonas J; Kumar, Parveen P; Møller, Elen K EK; Nord, Silje S; Wedge, David C DC; Peterson, April A; Mathiesen, Randi R RR; Fjelldal, Renathe R; Zamani Esteki, Masoud M; Theunis, Koen K; Fernandez Gallardo, Elia E; Grundstad, A Jason AJ; Borgen, Elin E; Baumbusch, Lars O LO; Børresen-Dale, Anne-Lise AL; White, Kevin P KP; Kristensen, Vessela N VN; Van Loo, Peter P; Voet, Thierry T; Naume, Bjørn B
Publication Date: 2016-12-09

Variant appearance in text: TM7SF2: Q153H
PubMed Link: 27931250
Variant Present in the following documents:
  • 13059_2016_1109_MOESM2_ESM.xlsx, sheet 5
View BVdb publication page