Gene

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

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 587

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



€ 587

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

** % 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




€ 587
Gene

COCH - autosomal dominant deafness type 9 (DFNA9)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 665

COCH - autosomal dominant deafness type 9 (DFNA9)



€ 665

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

** % 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




€ 665
Gene

COL11A2 - autosomal dominant deafness type 13 (DFNA13)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 946

COL11A2 - autosomal dominant deafness type 13 (DFNA13)



€ 946

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

** % 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




€ 946
Gene

DFNA5 - autosomal dominant deafness type 5

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 553

DFNA5 - autosomal dominant deafness type 5



€ 553

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

** % 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




€ 553
Gene

DIAPH1 - autosomal dominant deafness type 1 (DFNA1 )

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 811

DIAPH1 - autosomal dominant deafness type 1 (DFNA1 )



€ 811

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

** % 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




€ 811
Gene

EYA4 - autosomal dominant deafness type 10 (DFNA10 )

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 800

EYA4 - autosomal dominant deafness type 10 (DFNA10 )



€ 800

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

** % 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




€ 800
Gene

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

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 576

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



€ 576

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




€ 576
Gene

GJB3 - autosomal dominant deafness type 2B

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 576

GJB3 - autosomal dominant deafness type 2B



€ 576

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

** % 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




€ 576
Gene

GJB6 - autosomal dominant deafness type 3B

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 563

GJB6 - autosomal dominant deafness type 3B



€ 563

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




€ 563
Gene

GRHL2 - autosomal dominant deafness type 28

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 710

GRHL2 - autosomal dominant deafness type 28



€ 710

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

** % 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




€ 710
Gene

KCNQ4 - autosomal dominant deafness type 2 (DFNA2)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 688

KCNQ4 - autosomal dominant deafness type 2 (DFNA2)



€ 688

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

** % 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




€ 688
Gene

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

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 642

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



€ 642

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

** % 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




€ 642
Gene

MYH9 - autosomal dominant deafness type 17 (DFNA17)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 980

MYH9 - autosomal dominant deafness type 17 (DFNA17)



€ 980

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

** % 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




€ 980
Gene

MYO6 - autosomal dominant deafness type 22 (DFNA22)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 923

MYO6 - autosomal dominant deafness type 22 (DFNA22)



€ 923

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

** % 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




€ 923
Gene

MYO7A - autosomal dominant deafness type 11 (DFNA11)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 1069

MYO7A - autosomal dominant deafness type 11 (DFNA11)



€ 1069

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

** % 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




€ 1069
Gene

POU4F3 - autosomal dominant deafness type 15 (DFNA15 )

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 576

POU4F3 - autosomal dominant deafness type 15 (DFNA15 )



€ 576

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

** % 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




€ 576
Gene

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

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 845

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



€ 845

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

** % 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




€ 845
Gene

TMC1 - autosomal dominant deafness type 36 (DFNA36)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 778

TMC1 - autosomal dominant deafness type 36 (DFNA36)



€ 778

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

** % 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




€ 778
Gene

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

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 665

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



€ 665

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

** % 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




€ 665