×
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
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
GeneticVariation
group
CLINVAR
Combined Microsatellite Instability, MLH1 Methylation Analysis, and Immunohistochemistry for Lynch Syndrome Screening in Endometrial Cancers From GOG210: An NRG Oncology and Gynecologic Oncology Group Study.
26552419 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
25980754 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
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
0.100
CausalMutation
group
CLINVAR
Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel.
25186627 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
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
0.100
CausalMutation
group
CLINVAR
Multigene panel analysis identified germline mutations of DNA repair genes in breast and ovarian cancer.
26436112 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Genetic features of Lynch syndrome in the Israeli population.
25430799 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort.
26318770 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Combined Microsatellite Instability, MLH1 Methylation Analysis, and Immunohistochemistry for Lynch Syndrome Screening in Endometrial Cancers From GOG210: An NRG Oncology and Gynecologic Oncology Group Study.
26552419 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Lynch-like syndrome: characterization and comparison with EPCAM deletion carriers.
25110875 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.
26023681 2015
×
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
0.100
GeneticVariation
group
CLINVAR
[Constitutional mismatch repair deficiency syndrome].
26200421 2015