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.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Disease     

ID_report     

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VIP     

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Owner     
+?/? 32i c.4105-2A>T r.spl p.? - Maternal (confirmed) ACMG VUS g.73493995A>T g.71734238A>T - - CDH23_000363 heterozygous PubMed: Glöcke 2013 - - Germline - - +BseYI;-HpyCH4V;-PstI;-SbfI;-SfcI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/. - c.4105-2A>T r.spl p.(?) - Parent #1 - likely pathogenic g.73493995A>T g.71734238A>T CDH23, variant 1: c.4105-2A>T/p.?, variant 2: c.7362+5G>A/p.? - CDH23_000363 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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