|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
GeneticVariation
|
group |
CLINVAR |
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
|
28514183 |
2017 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
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: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
GeneticVariation
|
group |
CLINVAR |
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
|
27978560 |
2017 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Atypical dermal melanocytosis: a diagnostic clue in constitutional mismatch repair deficiency syndrome.
|
28369758 |
2017 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
|
27696107 |
2017 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
GeneticVariation
|
group |
CLINVAR |
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.
|
28944238 |
2017 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
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: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
GeneticVariation
|
group |
CLINVAR |
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity.
|
28531214 |
2017 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel.
|
26687385 |
2016 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients.
|
26483394 |
2016 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
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: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Germline multi-gene hereditary cancer panel testing in an unselected endometrial cancer cohort.
|
27443514 |
2016 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
|
26787237 |
2016 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
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: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
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: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity.
|
26544533 |
2016 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
|
27064304 |
2016 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
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: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Identification of germline genetic mutations in patients with pancreatic cancer.
|
26440929 |
2015 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
|
25980754 |
2015 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort.
|
26318770 |
2015 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population.
|
25318681 |
2015 |
|
| Entrez Id: |
2956 |
| Gene Symbol: |
MSH6 |
MSH6
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Lynch-like syndrome: characterization and comparison with EPCAM deletion carriers.
|
25110875 |
2015 |