MSH6 c.2101T>G ;(p.L701V)

Variant ID: 2-48027223-T-G

NM_000179.2(MSH6):c.2101T>G;(p.L701V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Concurrent CIC mutations, IDH mutations, and 1p/19q loss distinguish oligodendrogliomas from other cancers.

The Journal Of Pathology
Yip, Stephen S; Butterfield, Yaron S YS; Morozova, Olena O; Chittaranjan, Suganthi S; Blough, Michael D MD; An, Jianghong J; Birol, Inanc I; Chesnelong, Charles C; Chiu, Readman R; Chuah, Eric E; Corbett, Richard R; Docking, Rod R; Firme, Marlo M; Hirst, Martin M; Jackman, Shaun S; Karsan, Aly A; Li, Haiyan H; Louis, David N DN; Maslova, Alexandra A; Moore, Richard R; Moradian, Annie A; Mungall, Karen L KL; Perizzolo, Marco M; Qian, Jenny J; Roldan, Gloria G; Smith, Eric E EE; Tamura-Wells, Jessica J; Thiessen, Nina N; Varhol, Richard R; Weiss, Samuel S; Wu, Wei W; Young, Sean S; Zhao, Yongjun Y; Mungall, Andrew J AJ; Jones, Steven J M SJ; Morin, Gregg B GB; Chan, Jennifer A JA; Cairncross, J Gregory JG; Marra, Marco A MA
Publication Date: 2012-01

Variant appearance in text: MSH6: 2101T>G
PubMed Link: 22072542
Variant Present in the following documents:
  • Main text
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