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.

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/- 70 c.9873G>A r.9873g>a p.= Cytoplasmic (3086-3354) Paternal (inferred) - benign g.73574843G>A g.71815086G>A - - CDH23_000097 homozygous PubMed: Roux 2011 - rs2290021 Germline - - +BtsI;+TspRI;-Fnu4HI;-ApeKI;-BbvI;-TseI; - - DNA, RNA RT-PCR, SEQ - - USH1 - PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 70 c.9873G>A r.9873g>a p.= Cytoplasmic (3086-3354) Maternal (inferred) - benign g.73574843G>A g.71815086G>A - - CDH23_000097 homozygous PubMed: Roux 2011 - rs2290021 Germline - - +BtsI;+TspRI;-Fnu4HI;-ApeKI;-BbvI;-TseI; - - DNA, RNA RT-PCR, SEQ - - USH1 - PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 70 c.9873G>A r.(?) p.(=) Cytoplasmic (3086-3354) Paternal (inferred) - benign g.73574843G>A g.71815086G>A - - CDH23_000097 homozygous PubMed: Roux 2011 - rs2290021 Germline - - +BtsI;+TspRI;-Fnu4HI;-ApeKI;-BbvI;-TseI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - Italy - - - - - 1 Anne-Françoise Roux
-/- 70 c.9873G>A r.(?) p.(=) Cytoplasmic (3086-3354) Maternal (inferred) - benign g.73574843G>A g.71815086G>A - - CDH23_000097 homozygous PubMed: Roux 2011 - rs2290021 Germline - - +BtsI;+TspRI;-Fnu4HI;-ApeKI;-BbvI;-TseI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - Italy - - - - - 1 Anne-Françoise Roux
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.