Clinical Indication ID & Name
Rhabdoid Tumours - Paediatric
Test Group
Paediatric
Specialties
Test code
M167.1
Test name
Multi-target NGS panel - small variant (SMARCB1)
Target genes
SMARCB1
Test scope
Small variant detection
Test method/ technology
Panel
Optimal Family Structure
n/a
Eligibility Criteria
Specialist paediatric pathology review indicates that molecular assessment will aid diagnosis or management
Test code
M167.2
Test name
SMARCB1 seq
Target genes
SMARCB1
Test scope
Small variant detection
Test method/ technology
Single gene sequencing
Optimal Family Structure
n/a
Eligibility Criteria
Specialist paediatric pathology review indicates that molecular assessment will aid diagnosis or management
Test code
M167.3
Test name
SMARCB1 copy number FISH
Target genes
SMARCB1
Test scope
Copy number variant detection to genomewide resolution
Test method/ technology
FISH
Optimal Family Structure
n/a
Eligibility Criteria
Specialist paediatric pathology review indicates that molecular assessment will aid diagnosis or management
Test code
M167.4
Test name
WGS Germline and Tumour
Target genes
All including burden / signature
Test scope
All variant types
Test method/ technology
WGS
Optimal Family Structure
n/a
Eligibility Criteria
Specialist paediatric pathology review indicates that molecular assessment will aid diagnosis or management
Test code
M167.5
Test name
Multi-target NGS panel - structural variant (NTRK1, NTRK2, NTRK3)
Target genes
NTRK1, NTRK2, NTRK3
Test scope
Structural variant detection
Test method/ technology
Panel
Optimal Family Structure
n/a
Eligibility Criteria
Patient’s clinical status means they are eligible for an NTRK inhibitor in the event an NTRK rearrangement is detected
Test code
M167.6
Test name
Multi-target NGS panel - copy number variant (SMARCB1)
Target genes
SMARCB1
Test scope
Copy number variant detection to exon level resolution
Test method/ technology
Panel
Optimal Family Structure
n/a
Eligibility Criteria
Specialist paediatric pathology review indicates that molecular assessment will aid diagnosis or management
Commissioning group
n/a
Overlapping idications
n/a
Address for samples/request forms
North Thames GLH, Rare & Inherited Disease Genomic Laboratory
Specimen Reception, Level 5 Barclay House, 37 Queen Square,
London WC1N 3BH
Contact with queries
Supporting documents
n/a
Education resources
n/a
Service updates
n/a
Request form download
n/a
Consent record
See consent guidance in test request form
Sample requirements
See sample guidance in test request form