Gene

ACTG1 - autosomal dominant deafness type 20 (DFNA20/26)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 352

ACTG1 - autosomal dominant deafness type 20 (DFNA20/26)



€ 352

ACTG1 - autosomal dominant deafness type 20 (DFNA20/26)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 102560
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 352
Gene

COCH - autosomal dominant deafness type 9 (DFNA9)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 410

COCH - autosomal dominant deafness type 9 (DFNA9)



€ 410

COCH - autosomal dominant deafness type 9 (DFNA9)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 603196
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 410
Gene

COL11A2 - autosomal dominant deafness type 13 (DFNA13)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 616

COL11A2 - autosomal dominant deafness type 13 (DFNA13)



€ 616

COL11A2 - autosomal dominant deafness type 13 (DFNA13)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 120290
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 616
Gene

DFNA5 - autosomal dominant deafness type 5

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 327

DFNA5 - autosomal dominant deafness type 5



€ 327

DFNA5 - autosomal dominant deafness type 5

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of selected exons and flanking intron-exon boundaries
  • PCR followed by fragment (length) analysis
Remarks
All described mutations in DFNA5 result in the absence of exon 8 (193 bp) in the mRNA, causing a frame shift starting at aminoacid 330

OMIM: 608798
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 327
Gene

DIAPH1 - autosomal dominant deafness type 1 (DFNA1 )

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 517

DIAPH1 - autosomal dominant deafness type 1 (DFNA1 )



€ 517

DIAPH1 - autosomal dominant deafness type 1 (DFNA1 )

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 602121
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 517
Gene

EYA4 - autosomal dominant deafness type 10 (DFNA10 )

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 509

EYA4 - autosomal dominant deafness type 10 (DFNA10 )



€ 509

EYA4 - autosomal dominant deafness type 10 (DFNA10 )

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 603550
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 509
Gene

GJB2/GJB6 - autosomal dominant deafness type 3 (DFNA3)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 344

GJB2/GJB6 - autosomal dominant deafness type 3 (DFNA3)



€ 344

GJB2/GJB6 - autosomal dominant deafness type 3 (DFNA3)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
Remarks
Autosomal deafness type 3 (DFNA3) is caused either by a mutation in GJB2 or GJB6. Both genes will be analysed.

OMIM: 121011
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 344
Gene

GJB3 - autosomal dominant deafness type 2B

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 344

GJB3 - autosomal dominant deafness type 2B



€ 344

GJB3 - autosomal dominant deafness type 2B

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 603324
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 344
Gene

GJB6 - autosomal dominant deafness type 3B

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 336

GJB6 - autosomal dominant deafness type 3B



€ 336

GJB6 - autosomal dominant deafness type 3B

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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

Method

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

OMIM: 604418
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 336
Gene

GRHL2 - autosomal dominant deafness type 28

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 443

GRHL2 - autosomal dominant deafness type 28



€ 443

GRHL2 - autosomal dominant deafness type 28

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 608576
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 443
Gene

KCNQ4 - autosomal dominant deafness type 2 (DFNA2)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 426

KCNQ4 - autosomal dominant deafness type 2 (DFNA2)



€ 426

KCNQ4 - autosomal dominant deafness type 2 (DFNA2)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 603537
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 426
Gene

KITLG - autosomal dominant deafness type 69, unilateral or asymmetric (DFNA69)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 393

KITLG - autosomal dominant deafness type 69, unilateral or asymmetric (DFNA69)



€ 393

KITLG - autosomal dominant deafness type 69, unilateral or asymmetric (DFNA69)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 184745
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 393
Gene

MYH9 - autosomal dominant deafness type 17 (DFNA17)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 641

MYH9 - autosomal dominant deafness type 17 (DFNA17)



€ 641

MYH9 - autosomal dominant deafness type 17 (DFNA17)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 160775
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 641
Gene

MYO6 - autosomal dominant deafness type 22 (DFNA22)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 600

MYO6 - autosomal dominant deafness type 22 (DFNA22)



€ 600

MYO6 - autosomal dominant deafness type 22 (DFNA22)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 600970
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 600
Gene

MYO7A - autosomal dominant deafness type 11 (DFNA11)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 707

MYO7A - autosomal dominant deafness type 11 (DFNA11)



€ 707

MYO7A - autosomal dominant deafness type 11 (DFNA11)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 276903
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 707
Gene

POU4F3 - autosomal dominant deafness type 15 (DFNA15 )

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 344

POU4F3 - autosomal dominant deafness type 15 (DFNA15 )



€ 344

POU4F3 - autosomal dominant deafness type 15 (DFNA15 )

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 602460
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 344
Gene

TECTA - autosomal dominant deafness type 8/12 (DFNA8/12)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 542

TECTA - autosomal dominant deafness type 8/12 (DFNA8/12)



€ 542

TECTA - autosomal dominant deafness type 8/12 (DFNA8/12)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 602574
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 542
Gene

TMC1 - autosomal dominant deafness type 36 (DFNA36)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 492

TMC1 - autosomal dominant deafness type 36 (DFNA36)



€ 492

TMC1 - autosomal dominant deafness type 36 (DFNA36)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 606706
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 492
Gene

WFS1 - autosomal dominant deafness type 6/14 (DFNA6/14)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 410

WFS1 - autosomal dominant deafness type 6/14 (DFNA6/14)



€ 410

WFS1 - autosomal dominant deafness type 6/14 (DFNA6/14)

This test is available for the following conditions:

  • Conditions > Hearing impairment > Deafness, autosomal dominant

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: 8 weeks / Targeted analysis: 4 weeks

Method

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

OMIM: 606201
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 410