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.

6 entries on 1 page. Showing entries 1 - 6.
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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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 35 c.4309C>T r.(?) p.(Arg1437*) Cadherin 14 (1420-1527) Parent #2 - pathogenic g.73498354C>T g.71738597C>T - - CDH23_000047 heterozygous PubMed: Roux 2006 - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Roux 2006 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 35 c.4309C>T r.(?) p.(Arg1437*) Cadherin 14 (1420-1527) Parent #2 - pathogenic g.73498354C>T g.71738597C>T - - CDH23_000047 heterozygous PubMed: Roux 2006 - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Roux 2006 Relative F - France - - - - - 1 Anne-Françoise Roux
+/. - c.4309C>T r.(?) p.(Arg1437*) - Parent #1 - pathogenic g.73498354C>T g.71738597C>T - - CDH23_000047 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs397517329 Germline - 1/2781 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
+/. - c.4309C>T r.(?) p.(Arg1437*) - Unknown - pathogenic g.73498354C>T g.71738597C>T CDH23 c.4309C>T, p.Arg1442Ter - CDH23_000047 different transcript, error in annotation NM_022124.5(CDH23):c.4309C>T, p.(Arg1437*), heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI2858_004443 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.4309C>T r.(?) p.(Arg1437*) - Parent #1 - likely pathogenic g.73498354C>T g.71738597C>T CDH23, variant 1: c.4309C>T/p.R1437*, variant 2: c.4309C>T/p.R1437* - CDH23_000047 solved, homozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET4 targeted sequencing panel - see paper retinal disease 66 PubMed: Weisschuh 2020 Filing key number: 33, Usher syndrome type I, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.4309C>T r.(?) p.(Arg1437*) - Parent #1 - likely pathogenic g.73498354C>T g.71738597C>T CDH23, variant 1: c.4309C>T/p.R1437*, variant 2: c.4309C>T/p.R1437* - CDH23_000047 solved, homozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 67 PubMed: Weisschuh 2020 Filing key number: 33, Usher syndrome type I, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
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