×
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
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
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
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
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
Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases.
25892863
2015