MSH6 c.1742dup ;(p.F582Ifs*2)

Variant ID: 2-48026863-A-AG

NM_000179.2(MSH6):c.1742dup;(p.F582Ifs*2)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.

Nature Communications
Chubb, Daniel D; Broderick, Peter P; Dobbins, Sara E SE; Frampton, Matthew M; Kinnersley, Ben B; Penegar, Steven S; Price, Amy A; Ma, Yussanne P YP; Sherborne, Amy L AL; Palles, Claire C; Timofeeva, Maria N MN; Bishop, D Timothy DT; Dunlop, Malcolm G MG; Tomlinson, Ian I; Houlston, Richard S RS
Publication Date: 2016-06-22

Variant appearance in text: MSH6: 1742dupG
PubMed Link: 27329137
Variant Present in the following documents:
  • Main text
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