Panel

panel hereditary paragangliomas (SDHA, SDHB, SDHC, SDHD, SDHAF2)

Turnaround time
3 weeks
Performing laboratory
Radboudumc
€ 1550

panel hereditary paragangliomas (SDHA, SDHB, SDHC, SDHD, SDHAF2)



€ 1550

panel hereditary paragangliomas (SDHA, SDHB, SDHC, SDHD, SDHAF2)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

Turnaround time
3 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)

Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 1550
Panel

panel paragangliomas / pheochromocytomas (SDHA,SDHB,SDHC,SDHD,SDHAF2,RET,VHL,TMEM127,MAX,FH,MDH2)

Turnaround time
3 weeks
Performing laboratory
Radboudumc
€ 1550

panel paragangliomas / pheochromocytomas (SDHA,SDHB,SDHC,SDHD,SDHAF2,RET,VHL,TMEM127,MAX,FH,MDH2)



€ 1550

panel paragangliomas / pheochromocytomas (SDHA,SDHB,SDHC,SDHD,SDHAF2,RET,VHL,TMEM127,MAX,FH,MDH2)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

Turnaround time
3 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)
Remarks
Deletion/duplication analysis includes the SDH-, VHL and BAP1 gene.

Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 1550
Gene

FH - hereditary paragangliomas and pheochromocytomas

Turnaround time
Complete analysis & Targeted analysis: 3 weeks
Performing laboratory
Radboudumc
€ 1000

FH - hereditary paragangliomas and pheochromocytomas



€ 1000

FH - hereditary paragangliomas and pheochromocytomas

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

This product is also part of the following panels:

** % 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 & Targeted analysis: 3 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)

OMIM: 136850
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 1000
Gene

MAX - hereditary paraganglioma and feochromocytoma

Turnaround time
Complete analysis & Targeted analysis: 3 weeks
Performing laboratory
Radboudumc
€ 800

MAX - hereditary paraganglioma and feochromocytoma



€ 800

MAX - hereditary paraganglioma and feochromocytoma

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

This product is also part of the following panels:

** % 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 & Targeted analysis: 3 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
Remarks
Deletion/duplication analysis is being developed

OMIM: 154950
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 800
Gene

MDH2 - hereditary paraganglioma and feochromocytoma

Turnaround time
Complete analysis & Targeted analysis: 3 weeks
Performing laboratory
Radboudumc
€ 800

MDH2 - hereditary paraganglioma and feochromocytoma



€ 800

MDH2 - hereditary paraganglioma and feochromocytoma

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

This product is also part of the following panels:

** % 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 & Targeted analysis: 3 weeks

Method

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

OMIM: 154100
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 800
Gene

RET - paraganglioma / pheochromocytoma (MEN2)

Turnaround time
Complete analysis & Targeted analysis: 3 weeks
Performing laboratory
Radboudumc
€ 800

RET - paraganglioma / pheochromocytoma (MEN2)



€ 800

RET - paraganglioma / pheochromocytoma (MEN2)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

This product is also part of the following panels:

** % 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 & Targeted analysis: 3 weeks

Method

  • Sequence analysis of selected exons and flanking intron-exon boundaries
Remarks
Analysis of exons 10, 11, 13-16 only. With this test all known mutations are detected and explain 98% of the MEN2 patients.

OMIM: 164761
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 800
Gene

SDHA - hereditary paraganglioma and pheochromocytoma

Turnaround time
3 weeks
Performing laboratory
Radboudumc
€ 800

SDHA - hereditary paraganglioma and pheochromocytoma



€ 800

SDHA - hereditary paraganglioma and pheochromocytoma

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

This product is also part of the following panels:

** % 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
3 weeks

Method

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

OMIM: 600857
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 800
Gene

SDHAF2 - hereditary paraganglioma and pheochromocytoma

Turnaround time
Complete analysis & Targeted analysis: 3 weeks
Performing laboratory
Radboudumc
€ 800

SDHAF2 - hereditary paraganglioma and pheochromocytoma



€ 800

SDHAF2 - hereditary paraganglioma and pheochromocytoma

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

This product is also part of the following panels:

** % 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 & Targeted analysis: 3 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)

OMIM: 613019
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 800
Gene

SDHB - hereditary paraganglioma and pheochromocytoma

Turnaround time
3 weeks
Performing laboratory
Radboudumc
€ 1000

SDHB - hereditary paraganglioma and pheochromocytoma



€ 1000

SDHB - hereditary paraganglioma and pheochromocytoma

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

This product is also part of the following panels:

** % 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
3 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)

OMIM: 185470
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 1000
Gene

SDHC - hereditary paraganglioma and pheochromocytoma

Turnaround time
3 weeks
Performing laboratory
Radboudumc
€ 800

SDHC - hereditary paraganglioma and pheochromocytoma



€ 800

SDHC - hereditary paraganglioma and pheochromocytoma

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

This product is also part of the following panels:

** % 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
3 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)

OMIM: 602413
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 800
Gene

SDHD - hereditary paraganglioma and pheochromocytoma

Turnaround time
3 weeks
Performing laboratory
Radboudumc
€ 1000

SDHD - hereditary paraganglioma and pheochromocytoma



€ 1000

SDHD - hereditary paraganglioma and pheochromocytoma

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

This product is also part of the following panels:

** % 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
3 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)

OMIM: 602690
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 1000
Gene

TMEM127 - hereditary pheochromocytoma

Turnaround time
Complete analysis & Targeted analysis: 3 weeks
Performing laboratory
Radboudumc
€ 800

TMEM127 - hereditary pheochromocytoma



€ 800

TMEM127 - hereditary pheochromocytoma

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

This product is also part of the following panels:

** % 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 & Targeted analysis: 3 weeks

Method

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

OMIM: 613403
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 800
Gene

VHL - hereditary paragangliomas and pheochromocytomas

Turnaround time
3 weeks
Performing laboratory
Radboudumc
€ 1000

VHL - hereditary paragangliomas and pheochromocytomas



€ 1000

VHL - hereditary paragangliomas and pheochromocytomas

This test is available for the following conditions:

  • Conditions > Hearing impairment > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Endocrine > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Renal / Nephrological > Paraganglioma and pheochromocytoma, Hereditary
  • Conditions > Oncogenetics > Paraganglioma and pheochromocytoma, Hereditary

This product is also part of the following panels:

** % 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
3 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)

OMIM: 608537
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA




€ 1000