Melanoma-pancreatic cancer syndrome

CDKN2A - melanoma-pancreatic cancer syndrome ¹

This test is available for the following conditions:

• Conditions > Skin > Melanoma-pancreatic cancer syndrome
• Conditions > Oncogenetics > Melanoma-pancreatic cancer syndrome

This product is also part of the following panels:

• panel Melanoma, basic (CDKN2A, CDK4, MITF p.(Glu318Lys)¹
• panel Melanoma, basic (CDKN2A, CDK4, MITF p.(Glu318Lys)¹
• panel Melanoma, extensive (CDKN2A, CDK4, MITF p.(Glu318Lys), BAP1, POT1, TERT promoter)¹
• panel Melanoma, extensive (CDKN2A, CDK4, MITF p.(Glu318Lys), BAP1, POT1, TERT promoter)¹
• WES hereditary cancer (100.0% *)
• WES Mendelian inherited disorders (100.0% *)
• WES skin disorders¹ (100.0% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

• Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 600160
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

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