Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease CLINVAR Spectrum of APC and MUTYH germ-line mutations in Russian patients with colorectal malignancies. 29406563 2018
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 CausalMutation disease 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
0.710 CausalMutation disease 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
0.710 CausalMutation disease CLINVAR Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer. 27978560 2017
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease 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
0.710 Biomarker disease CLINGEN Repair of 8-oxoG:A mismatches by the MUTYH glycosylase: Mechanism, metals and medicine. 28087410 2017
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease CLINVAR The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies. 28349240 2017
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 CausalMutation disease CLINVAR Mutational signature analysis identifies MUTYH deficiency in colorectal cancers and adrenocortical carcinomas. 28127763 2017
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease CLINVAR Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary. 26446593 2016
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease CLINVAR Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH. 27194394 2016
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease CLINVAR Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer. 26824983 2016
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 CausalMutation disease CLINVAR Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH. 27194394 2016
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease 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
0.710 CausalMutation disease CLINVAR Inactivating MUTYH germline mutations in pediatric patients with high-grade midline gliomas. 26902849 2016
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease UNIPROT 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
0.710 CausalMutation disease CLINVAR Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary. 26446593 2016
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 CausalMutation disease CLINVAR Detection of inherited mutations for hereditary cancer using target enrichment and next generation sequencing. 25151137 2015
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease CLINVAR MUTYH mediates the toxicity of combined DNA 6-thioguanine and UVA radiation. 25638157 2015
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease CLINVAR Distinct functional consequences of MUTYH variants associated with colorectal cancer: Damaged DNA affinity, glycosylase activity and interaction with PCNA and Hus1. 26377631 2015
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease 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
0.710 CausalMutation disease CLINVAR Patterns and functional implications of rare germline variants across 12 cancer types. 26689913 2015
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 CausalMutation disease CLINVAR Genomic variations integrated database for MUTYH-associated adenomatous polyposis. 25368107 2015
Entrez Id: 4595
Gene Symbol: MUTYH
MUTYH
0.710 GeneticVariation disease 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
0.710 CausalMutation disease 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
0.710 CausalMutation disease CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159 2015