×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
27696107 2017
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Atypical dermal melanocytosis: a diagnostic clue in constitutional mismatch repair deficiency syndrome.
28369758 2017
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
GeneticVariation
group
CLINVAR
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
28514183 2017
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.
28195393 2017
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
GeneticVariation
group
CLINVAR
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity.
28531214 2017
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
GeneticVariation
group
CLINVAR
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
27978560 2017
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
GeneticVariation
group
CLINVAR
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.
28944238 2017
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Gene panel sequencing in familial breast/ovarian cancer patients identifies multiple novel mutations also in genes others than BRCA1/2.
27616075 2017
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
GeneticVariation
group
CLINVAR
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
26681312 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Improving performance of multigene panels for genomic analysis of cancer predisposition.
26845104 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel.
26687385 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients.
26483394 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Germline multi-gene hereditary cancer panel testing in an unselected endometrial cancer cohort.
27443514 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity.
26544533 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
26681312 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
27601186 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
26787237 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
27064304 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
A cohort analysis of men with a family history of BRCA1/2 and Lynch mutations for prostate cancer.
27456091 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Prognostic impact of mismatch repair genes germline defects in colorectal cancer patients: are all mutations equal?
26485756 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Clinical and Molecular Characterization of Brazilian Patients Suspected to Have Lynch Syndrome.
26437257 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
GeneticVariation
group
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: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndrome.
25782445 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment.
26270727 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Identification of germline genetic mutations in patients with pancreatic cancer.
26440929 2015