Varaico: Literature-Extracted Genetic Variants

Gene:MSH2
Variant:p.Q324H
Back to variants list

MSH2

NM_000251.3:p.Q324H

Associated Papers

Genetic variants in MUTYH are not associated with endometrial cancer risk.

Ashton KA et al.

Hereditary Cancer in Clinical Practice, 2009

Characterization of mutant MUTYH proteins associated with familial colorectal cancer.

Ali M et al.

Gastroenterology, 2008

Association between genetic polymorphisms of the base excision repair gene MUTYH and increased colorectal cancer risk in a Japanese population.

Tao H et al.

Cancer Science, 2008

Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis.

Cattaneo F et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2007

Identification of MYH mutation carriers in colorectal cancer: a multicenter, case-control, population-based study.

Balaguer F et al.

Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association, 2007

Implication of MYH in colorectal polyposis.

Lefevre JH et al.

Annals of Surgery, 2006

The role of MYH and microsatellite instability in the development of sporadic colorectal cancer.

Colebatch A et al.

British Journal of Cancer, 2006

Microsatellite stable colorectal cancers in clinically suspected hereditary nonpolyposis colorectal cancer patients without vertical transmission of disease are unlikely to be caused by biallelic germline mutations in MYH.

Görgens H et al.

The Journal of Molecular Diagnostics : Jmd, 2006

Germline mutations in the MYH gene in Swedish familial and sporadic colorectal cancer.

Zhou XL et al.

Genetic Testing, 2005

A novel splice-site variant of the base excision repair gene MYH is associated with production of an aberrant mRNA transcript encoding a truncated MYH protein not localized in the nucleus.

Tao H et al.

Carcinogenesis, 2004

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."