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     
+/+ 43 c.5712G>A r.(?) p.(=) Cadherin 18 (1852-1959) Parent #1 - pathogenic g.73544857G>A g.71785100G>A - - CDH23_000008 heterozygous PubMed: von Brederlow 2002 - - Germline - 0/100 controls -BsaJI;-BtgI; - - DNA SEQ - - USH1 - PubMed: von Brederlow 2002 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 43 c.5712G>A r.(?) p.(=) Cadherin 18 (1852-1959) Paternal (inferred) - pathogenic g.73544857G>A g.71785100G>A - - CDH23_000008 homozygous; Mutation PubMed: Vozzi 2011 - - Germline - - -BsaJI;-BtgI; - - DNA PE, SEQ - APEX USH1 - PubMed: Vozzi 2011 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 43 c.5712G>A r.(?) p.(=) Cadherin 18 (1852-1959) Maternal (inferred) - pathogenic g.73544857G>A g.71785100G>A - - CDH23_000008 homozygous; Mutation PubMed: Vozzi 2011 - - Germline - - -BsaJI;-BtgI; - - DNA PE, SEQ - APEX USH1 - PubMed: Vozzi 2011 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+?/. - c.5712G>A r.spl p.? - Parent #1 - likely pathogenic g.73544857G>A - - - CDH23_000008 - PubMed: Holtan 2020 - - Germline - 1/899 cases - - - DNA SEQ - - retinal disease - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - 1 Global Variome, with Curator vacancy
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