×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
UMD-MLH1/MSH2/MSH6 databases: description and analysis of genetic variations in French Lynch syndrome families.
23729658 2013
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Type and frequency of MUTYH variants in Italian patients with suspected MAP: a retrospective multicenter study.
27829682 2017
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
The thorough screening of the MUTYH gene in a large French cohort of sporadic colorectal cancers.
17931073 2007
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
The potential for increased clinical sensitivity in genetic testing for polyposis colorectal cancer through the analysis of MYH mutations in North American patients.
15635083 2005
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
The genetic basis of familial adenomatous polyposis and its implications for clinical practice and risk management.
25931827 2015
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.
28944238 2017
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Simplifying the detection of MUTYH mutations by high resolution melting analysis.
20687945 2010
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Similar colorectal cancer risk in patients with monoallelic and biallelic mutations in the MYH gene identified in a population with adenomatous polyposis.
17949294 2007
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Similar colorectal cancer risk in patients with monoallelic and biallelic mutations in the MYH gene identified in a population with adenomatous polyposis.
17949294 2007
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.
22703879 2012
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Sebaceous adenomas in an MYH associated polyposis patient of Indian (Gujarati) origin.
17874208 2008
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
25525159 2015
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH.
27194394 2016
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer.
24444654 2014
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Relative and absolute risk of colorectal cancer for individuals with a family history: a meta-analysis.
16338133 2006
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Reduced expression of the DNA glycosylase gene MUTYH is associated with an increased number of somatic mutations via a reduction in the DNA repair capacity in prostate adenocarcinoma.
27253753 2017
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Racial variation in frequency and phenotypes of APC and MUTYH mutations in 6,169 individuals undergoing genetic testing.
25590978 2015
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Prevalence of MYH germline mutations in Swiss APC mutation-negative polyposis patients.
16287072 2006
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Prevalence of MYH germline mutations in Swiss APC mutation-negative polyposis patients.
16287072 2006
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Prevalence and characteristics of MUTYH-associated polyposis in patients with multiple adenomatous and serrated polyps.
24470512 2014
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Personalized genomic disease risk of volunteers.
24082139 2013
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
26681312 2016
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Novel mutations and phenotypic associations identified through APC, MUTYH, NTHL1, POLD1, POLE gene analysis in Indian Familial Adenomatous Polyposis cohort.
28533537 2017
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Novel findings in Swedish patients with MYH-associated polyposis: mutation detection and clinical characterization.
16616356 2006
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
18301448 2008