Clinical Indication ID & Name
Familial rhabdoid tumours
Test Group
Inherited cancer
Specialties
Test code
R358.1
Test name
N/A
Target genes
Rhabdoid tumour predisposition (600)
Test scope
n/a
Test method/ technology
Small panel
Optimal Family Structure
n/a
Eligibility Criteria
Living affected individual (proband) where the proband has atypical teratoid/rhabdoid tumour (any age) OR
Small cell carcinoma of the ovary, hypercalcaemic type (SCCOHT) (any age)
NOTE: The proband’s cancer should have been confirmed
Genetic testing may occasionally be appropriate outside these criteria following discussion at a specialist MDT with a cancer geneticist present
Likely to need to specify high coverage depth to detect mosaic SMARCB1 and SMARCA4 mutations
Test code
R358.2
Test name
N/A
Target genes
Rhabdoid tumour predisposition (600)
Test scope
n/a
Test method/ technology
Exon level CNV detection by MLPA or equivalent
Optimal Family Structure
n/a
Eligibility Criteria
Living affected individual (proband) where the proband has atypical teratoid/rhabdoid tumour (any age) OR
Small cell carcinoma of the ovary, hypercalcaemic type (SCCOHT) (any age)
NOTE: The proband’s cancer should have been confirmed
Genetic testing may occasionally be appropriate outside these criteria following discussion at a specialist MDT with a cancer geneticist present
Likely to need to specify high coverage depth to detect mosaic SMARCB1 and SMARCA4 mutations
Commissioning group
Specialised
Overlapping idications
• M120 Atypical teratoid/rhabdoid tumour (ATRT) should be used for somatic testing
Address for samples/request forms
Genetics Laboratory
5th Floor Tower Wing
Guy’s Hospital
London
SE1 9RT
Contact with queries
Supporting documents
n/a
Education resources
n/a
Turn around times
All our turnaround times are listed on our specific turn around page https://southeastgenomics.nhs.uk/professionals/service-turn-around-times/
Request form download
Consent record
See consent guidance in test request form
Sample requirements
Samples may be rejected for the following reasons: 1.Samples and request form do not show at least three identical patient identifiers 2.The sample is in the incorrect collection media 3.The request form is not sufficiently completed 4.The sample is not of sufficient volume 5.The sample is too old