MSH6 c.2206G>C ;(p.D736H)

Variant ID: 2-48027328-G-C

NM_000179.2(MSH6):c.2206G>C;(p.D736H)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Thyroid cancers of follicular origin in a genomic light: in-depth overview of common and unique molecular marker candidates.

Molecular Cancer
Pstrąg, Natalia N; Ziemnicka, Katarzyna K; Bluyssen, Hans H; Wesoły, Joanna J
Publication Date: 2018-08-08

Variant appearance in text: MSH6: D736H
PubMed Link: 30089490
Variant Present in the following documents:
  • Main text
  • 12943_2018_Article_866.pdf
View BVdb publication page



Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing.

Human Molecular Genetics
Kunstman, John W JW; Juhlin, C Christofer CC; Goh, Gerald G; Brown, Taylor C TC; Stenman, Adam A; Healy, James M JM; Rubinstein, Jill C JC; Choi, Murim M; Kiss, Nimrod N; Nelson-Williams, Carol C; Mane, Shrikant S; Rimm, David L DL; Prasad, Manju L ML; Höög, Anders A; Zedenius, Jan J; Larsson, Catharina C; Korah, Reju R; Lifton, Richard P RP; Carling, Tobias T
Publication Date: 2015-04-15

Variant appearance in text: MSH6: D736H
PubMed Link: 25576899
Variant Present in the following documents:
  • Main text
View BVdb publication page