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.

2 entries on 1 page. Showing entries 1 - 2.
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     
+/+ 47 c.6155del r.(?) p.(Thr2052Argfs*28) Cadherin 19 (1960-2069) Parent #1 - pathogenic g.73550994del g.71791237del - - CDH23_000148 heterozygous PubMed: Astuto 2002 - - Germline - - - - - DNA SEQ - - USH - PubMed: Astuto 2002 Proband - - - European - - - - 1 Anne-Françoise Roux
+/+ 47 c.6155del r.(?) p.(Thr2052Argfs*28) Cadherin 19 (1960-2069) Parent #1 - pathogenic g.73550994del g.71791237del - - CDH23_000148 heterozygous PubMed: Astuto 2002 - - Germline - - - - - DNA SEQ - - USH - PubMed: Astuto 2002 Relative - - - European - - - - 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.