×
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
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
CausalMutation
CLINVAR
Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing.
28873162 2017
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Mutational signature analysis identifies MUTYH deficiency in colorectal cancers and adrenocortical carcinomas.
28127763 2017
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Association of monoallelic MUTYH mutation among Egyptian patients with colorectal cancer.
27631816 2017
×
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
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
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
Inactivating MUTYH germline mutations in pediatric patients with high-grade midline gliomas.
26902849 2016
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
27153395 2016
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Functional Evaluation of Nine Missense-Type Variants of the Human DNA Glycosylase Enzyme MUTYH in the Japanese Population.
26694661 2016
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer.
26976419 2016
×
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
Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary.
26446593 2016
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Cutaneous Sebaceous Lesions in a Patient With MUTYH-Associated Polyposis Mimicking Muir-Torre Syndrome.
27870730 2016
×
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
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
25980754 2015
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases.
25892863 2015
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases.
25892863 2015
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Functional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain.
25820570 2015
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
25980754 2015
×
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing.
25559809 2015
×
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
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
Detection of inherited mutations for hereditary cancer using target enrichment and next generation sequencing.
25151137 2015