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     

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     
-?/? 24 c.2591G>A r.(?) p.(Gly864Asp) Cadherin 8 (779-890) Paternal (inferred) ACMG likely benign g.73462309G>A g.71702552G>A - - CDH23_000188 homozygous PubMed: Ammar-Khodja 2009; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/120 controls +Tsp45I;+HphI;+Cac8I; - - DNA minigene, SEQ - - USH1 - PubMed: Ammar-Khodja 2009 Proband F - Algeria - - - - - 1 Anne-Françoise Roux
-?/? 24 c.2591G>A r.(?) p.(Gly864Asp) Cadherin 8 (779-890) Maternal (inferred) ACMG likely benign g.73462309G>A g.71702552G>A - - CDH23_000188 homozygous PubMed: Ammar-Khodja 2009; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/120 controls +Tsp45I;+HphI;+Cac8I; - - DNA minigene, SEQ - - USH1 - PubMed: Ammar-Khodja 2009 Proband F - Algeria - - - - - 1 Anne-Françoise Roux
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