Full data view for gene CDH23


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_022124.5 transcript reference sequence.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/? 55 c.7872G>A r.[(7872g>a; 7872_7873ins7872+1_7872+86)] p.[(=; Glu2625Valfs*30)] Cadherin 25 (2614-2722) Unknown ACMG likely pathogenic g.73563177G>A g.71803420G>A - - CDH23_000104 heterozygous PubMed: Astuto 2002 - - Germline - +ScaI;+MnlI; - - - DNA SEQ - - USH1 - PubMed: Astuto 2002 Proband - - - - - - - - 1 Anne-Françoise Roux
+/? 55 c.7872G>A r.[7872g>a; 7872_7873ins7872+1_7872+86] p.[=; Glu2625Valfs*30] Cadherin 25 (2614-2722) Parent #1 ACMG likely pathogenic g.73563177G>A g.71803420G>A - - CDH23_000104 heterozygous; ins first 86 nt IVS54 PubMed: Le Guédard-Méreuze 2010 - - Germline - 0/200 controls +ScaI;+MnlI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+/? 55 c.7872G>A r.[(7872g>a; 7872_7873ins7872+1_7872+86)] p.[(=; Glu2625Valfs*30)] Cadherin 25 (2614-2722) Maternal (confirmed) ACMG likely pathogenic g.73563177G>A g.71803420G>A - - CDH23_000104 heterozygous; Mutation PubMed: Schultz 2011 - - Germline - - +ScaI;+MnlI; - - DNA SEQ - - DFNB - PubMed: Schultz 2011 Proband - daughter 2 F - United States - - - - - 1 Anne-Françoise Roux
+/? 55 c.7872G>A r.[(7872g>a; 7872_7873ins7872+1_7872+86)] p.[(=; Glu2625Valfs*30)] Cadherin 25 (2614-2722) Unknown ACMG likely pathogenic g.73563177G>A g.71803420G>A - - CDH23_000104 heterozygous; Mutation PubMed: Schultz 2011 - - Germline - - +ScaI;+MnlI; - - DNA SEQ - - USH1 - PubMed: Schultz 2011 Proband - mother F - United States - - - - - 1 Anne-Françoise Roux
+/. 56 c.7872G>A r.spl p.? - Both (homozygous) - pathogenic (recessive) g.73563177G>A g.71803420G>A - - CDH23_000104 - Tranebjaerg 2011, PubMed: Dad 2016 - - Germline - - - - - DNA PE - - retinal disease USH1-21 Tranebjaerg 2011, PubMed: Dad 2016 family, 2 affeted M yes Pakistan - - - - - 2 LOVD
+/. 56 c.7872G>A r.spl p.? - Both (homozygous) - pathogenic (recessive) g.73563177G>A g.71803420G>A - - CDH23_000104 - Tranebjaerg 2011, PubMed: Dad 2016 - - Germline - - - - - DNA PE - - retinal disease USH1-21A Tranebjaerg 2011, PubMed: Dad 2016 - F yes Pakistan - - - - - 1 LOVD
+?/. 55 c.7872G>A r.(=) p.(=) - Unknown - likely pathogenic g.73563177G>A - c.7872G>A - CDH23_000104 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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