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  2. Colorectal cancer / Polyposis (gene panel)

Colorectal cancer / Polyposis (gene panel)

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Full name:
Colorectal cancer / Polyposis (gene panel)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis,
Predictive and Pre-symptomatic diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Sequence analysis: entire coding region
Deletion/duplication analysis
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centrum Menselijke Erfelijkheid - KUL
RIZIV code:
565552-565563
EQA:
  • 2015 Lynch Syndrome EMQN
  • 2016 Lynch Syndrome EMQN
  • 2017 Lynch Syndrome EMQN
  • 2017 Familial Adenomatous Polyposis Colon Cancer EMQN
  • 2018 Lynch Syndrome EMQN
  • 2018 Familial Adenomatous Polyposis Colon Cancer EMQN
  • 2021 Lynch Syndrome EMQN
  • 2021 Polyposis syndrome (Familial Adenomatous Polyposis Colon Cancer, MAP) EMQN
Accreditation (ISO 15189):
2021-07-08 / 2026-02-02
Turnaround time (maximum):
4 - 6 months
Document(s):
Created:
18 Jul 2019 - 11:23
Changed:
01 Mar 2023 - 14:53
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB%20CME/13379
  • Colorectal cancer/polyposis (18 genes) - KUL
    Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments
    MLH1 100.00 1
    MSH2 100.00 1
    MSH6 100.00 1
    PMS2 100.00 1
    EPCAM 100.00 1
    POLD1 100.00 1
    POLE 100.00 1
    CHEK2 100.00 1
    TP53 100.00 1
    APC 100.00 1
    STK11 100.00 1
    BMPR1A 100.00 1
    SMAD4 100.00 1
    PTEN 100.00 1
    RNF43 100.00 1
    NTHL1 100.00 1
    MSH3 100.00 1
    MUTYH 100.00 1