ATM - risk factor breast cancer
This test is available for the following conditions:
- Conditions > Oncogenetics > Breast and Ovary cancer, hereditary
This product is also part of the following panels:
- Comprehensive preconception carrier test panel¹
- Hereditary cancer panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- Movement disorders panel
- Panel hereditary pancreatic cancer (BRCA1, BRCA2, PALB2, ATM, CDKN2A, MLH1, MSH2, MSH6, PMS2, STK11)
- Primary immunodeficiencies panel
                Turnaround time
                Complete analysis & Targeted analysis: 3 weeks
            
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
                    OMIM: 
607585                    
                    Performing laboratory: Radboudumc & Maastricht UMC+
                    Authorized material(s): EDTA blood, FFPE, Isolated DNA
            
BARD1 - risk factor breast cancer
This test is available for the following conditions:
- Conditions > Oncogenetics > Breast and Ovary cancer, hereditary
                Turnaround time
                Complete analysis & Targeted analysis: 3 weeks
            
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
                    OMIM: 
601593                    
                    Performing laboratory: Radboudumc & Maastricht UMC+
                    Authorized material(s): EDTA blood, FFPE, Isolated DNA
            
BRCA1 - hereditary breast cancer and/or ovarian cancer (only familial mutation testing)
This test is available for the following conditions:
- Conditions > Oncogenetics > Breast and Ovary cancer, hereditary
This product is also part of the following panels:
- Comprehensive preconception carrier test panel¹
- Hereditary cancer panel
- Inherited bone marrow failure and/or predisposition panel to hematological malignancies
- Mendelian inherited disorders panel with genome wide CNV analysis
- Panel hereditary pancreatic cancer (BRCA1, BRCA2, PALB2, ATM, CDKN2A, MLH1, MSH2, MSH6, PMS2, STK11)
                Turnaround time
                Complete analysis & Targeted analysis: 3 weeks
            
Method
- Sequence analysis of selected exons and flanking intron-exon boundaries
Analysis of a known familial mutation only (screening).
                    OMIM: 
113705                    
                    Performing laboratory: Radboudumc & Maastricht UMC+
                    Authorized material(s): EDTA blood, FFPE, Isolated DNA
            
BRCA2 - hereditary breast cancer and/or ovarian cancer (only familial mutation testing)
This test is available for the following conditions:
- Conditions > Oncogenetics > Breast and Ovary cancer, hereditary
This product is also part of the following panels:
- Comprehensive preconception carrier test panel¹
- Hereditary cancer panel
- Inherited bone marrow failure and/or predisposition panel to hematological malignancies
- Mendelian inherited disorders panel with genome wide CNV analysis
- Panel hereditary pancreatic cancer (BRCA1, BRCA2, PALB2, ATM, CDKN2A, MLH1, MSH2, MSH6, PMS2, STK11)
- Sonic hedgehog medulloblastoma panel
                Turnaround time
                Complete analysis & Targeted analysis: 3 weeks
            
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
- Deletion/duplication analysis (MLPA)
Analysis of a known familial mutation only (screening).
MLPA analysis only upon request.
                    OMIM: 
600185                    
                    Performing laboratory: Radboudumc & Maastricht UMC+
                    Authorized material(s): EDTA blood, FFPE, Isolated DNA
            
BRIP1 - hereditary ovarian cancer (only familial mutation testing)
This test is available for the following conditions:
- Conditions > Oncogenetics > Breast and Ovary cancer, hereditary
                Turnaround time
                Complete analysis & Targeted analysis: 3 weeks
            
Method
- Sequence analysis of selected exons and flanking intron-exon boundaries
                    OMIM: 
605882                    
                    Performing laboratory: Radboudumc & Maastricht UMC+
                    Authorized material(s): EDTA blood, FFPE, Isolated DNA
            
CHEK2 - risk factor breast cancer
This test is available for the following conditions:
- Conditions > Oncogenetics > Breast and Ovary cancer, hereditary
This product is also part of the following panels:
- Hereditary cancer panel
- Mendelian inherited disorders panel with genome wide CNV analysis
                Turnaround time
                Complete analysis & Targeted analysis: 3 weeks
            
Method
- Sequence analysis of selected exons and flanking intron-exon boundaries
                    OMIM: 
604373                    
                    Performing laboratory: Radboudumc & Maastricht UMC+
                    Authorized material(s): EDTA blood, FFPE, Isolated DNA
            
PALB2 - hereditary breast cancer
This test is available for the following conditions:
- Conditions > Oncogenetics > Breast and Ovary cancer, hereditary
This product is also part of the following panels:
- Hereditary cancer panel
- Inherited bone marrow failure and/or predisposition panel to hematological malignancies
- Mendelian inherited disorders panel with genome wide CNV analysis
- Panel hereditary pancreatic cancer (BRCA1, BRCA2, PALB2, ATM, CDKN2A, MLH1, MSH2, MSH6, PMS2, STK11)
- Skin disorders panel¹
- Sonic hedgehog medulloblastoma panel
                Turnaround time
                Complete analysis & Targeted analysis: 3 weeks
            
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
                    OMIM: 
610355                    
                    Performing laboratory: Radboudumc & Maastricht UMC+
                    Authorized material(s): EDTA blood, FFPE, Isolated DNA
            
RAD51C - hereditary ovarian cancer (only familial mutation testing)
This test is available for the following conditions:
- Conditions > Oncogenetics > Breast and Ovary cancer, hereditary
                Turnaround time
                Complete analysis & Targeted analysis: 3 weeks
            
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
- Deletion/duplication analysis (MLPA)
MLPA analysis only upon request.
                    OMIM: 
613399                    
                    Performing laboratory: Radboudumc & Maastricht UMC+
                    Authorized material(s): EDTA blood, FFPE, Isolated DNA
            
RAD51D - hereditary ovarian cancer (only familial mutation testing)
This test is available for the following conditions:
- Conditions > Oncogenetics > Breast and Ovary cancer, hereditary
                Turnaround time
                Complete analysis & Targeted analysis: 3 weeks
            
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
- Deletion/duplication analysis (MLPA)
MLPA analysis only upon request.
                    OMIM: 
614291                    
                    Performing laboratory: Radboudumc & Maastricht UMC+
                    Authorized material(s): EDTA blood, FFPE, Isolated DNA
            
