Hereditary Melanoma Panel (7 genes)

Genetic test Export to PDF

Full name:	Hereditary Melanoma Panel (7 genes)
Description:	.
Test type:	Clinical
Test specialty:	Molecular Genetics
Test purpose:	Carrier diagnosis, Post-natal Diagnosis
Specimen:	Peripheral (whole) blood on EDTA, DNA
Method category:	Sequence analysis: entire coding region
Method technique:	Next Generation Sequencing (NGS)
Laboratory:	Centre de Génétique Humaine - CHU Sart-Tilman
RIZIV code:	565552-565563
Turnaround time (maximum):	2-3 months
Document(s):	Application form for hereditary cancer276.42 KB
Created:	22 Mar 2022 - 14:22
Changed:	23 Jan 2023 - 12:21
URL:	https://www.chu.ulg.ac.be/jcms/c_14209781/fr/susceptibilite-au-melanome

Related Diseases

• BAP1-related tumor predisposition syndrome
• Familial atypical multiple mole melanoma syndrome
• Familial melanoma
• MITF-related melanoma and renal cell carcinoma predisposition syndrome
• Melanoma and neural system tumor syndrome

Related Laboratories

• Centre de Génétique Humaine - CHU Sart-Tilman

Related Analytes

• BAP1
• CDK4
• CDKN2A
• MITF
• POT1
• TERF2IP
• TERT

Related Gene Panels

• Hereditary Melanoma Panel (7 genes) - ULG
  Details

  Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Copy number variation	Comments
  CDKN2A	100.00	0
  CDK4	100.00	0
  POT1	100.00	0
  TERT	100.00	0
  TERF2IP	100.00	0
  BAP1	100.00	0
  MITF	100.00	0