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.
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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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 52i c.7362+5G>A r.(?) p.(?) - Parent #1 - pathogenic g.73559391G>A g.71799634G>A - - CDH23_000004 heterozygous PubMed: Bolz 2001 - - Germline - 0/400 controls - - - DNA SEQ - - USH1 - PubMed: Bolz 2001 Proband M - Germany - - - - - 1 Anne-Françoise Roux
+/+ 52i c.7362+5G>A r.(?) p.(?) - Unknown - pathogenic g.73559391G>A g.71799634G>A - - CDH23_000004 heterozygous PubMed: von Brederlow 2002 - - Germline - 0/100 controls - - - DNA SEQ - - USH1 - PubMed: von Brederlow 2002 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 52i c.7362+5G>A r.(?) p.(?) - Paternal (confirmed) - pathogenic g.73559391G>A g.71799634G>A - - CDH23_000004 heterozygous; likely pathogenic PubMed: Glöcke 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/. - c.7362+5G>A r.spl? p.(?) - Parent #1 - likely pathogenic g.73559391G>A g.71799634G>A CDH23, variant 1: c.4105-2A>T/p.?, variant 2: c.7362+5G>A/p.? - CDH23_000004 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET1 targeted sequencing panel - see paper retinal disease 44 PubMed: Weisschuh 2020 Filing key number: 24, Usher syndrome type I, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
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