×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
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: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Analysis of Lynch Syndrome Mismatch Repair Genes in Women with Endometrial Cancer.
27398995 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancers.
26648449 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
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: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
26787237 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
27064304 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Co-occurrence of nonsense mutations in MSH6 and MSH2 in Lynch syndrome families evidencing that not all truncating mutations are equal.
26446363 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Mismatch repair deficiency concordance between primary colorectal cancer and corresponding metastasis.
26666765 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Massively Parallel Sequencing-Based Clonality Analysis of Synchronous Endometrioid Endometrial and Ovarian Carcinomas.
26832770 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Teenage colorectal polyposis and cancer may be caused by constitutional mismatch repair deficiency (CMMRD).
27723366 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
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
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
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
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
27601186 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Inherited Mutations in Women With Ovarian Carcinoma.
26720728 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Germline multi-gene hereditary cancer panel testing in an unselected endometrial cancer cohort.
27443514 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Frequent mismatch-repair defects link prostate cancer to Lynch syndrome.
27013479 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
27601186 2016
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Comprehensive screening for mutations associated with colorectal cancer in unselected cases reveals penetrant and nonpenetrant mutations.
25142776 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Impact of an immunohistochemistry-based universal screening protocol for Lynch syndrome in endometrial cancer on genetic counseling and testing.
25617771 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
The gastrointestinal manifestation of constitutional mismatch repair deficiency syndrome: from a single adenoma to polyposis-like phenotype and early onset cancer.
25307252 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Clinical and Molecular Characterization of Brazilian Patients Suspected to Have Lynch Syndrome.
26437257 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Germ-line variants identified by next generation sequencing in a panel of estrogen and cancer associated genes correlate with poor clinical outcome in Lynch syndrome patients.
26517685 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
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
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Identification of germline genetic mutations in patients with pancreatic cancer.
26440929 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
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