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     

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VIP     

Data_av     

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Panel size     

Owner     
-?/? 42 c.5418C>G r.(?) p.(Asp1806Glu) Cadherin 17 (1745-1851) Unknown - benign g.73544093C>G g.71784336C>G - - CDH23_000200 heterozygous PubMed: Kimberling 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs74145660 Germline - - +MnlI;+BslI;-HpyCH4IV;-BmgBI; - - DNA SEQ - - DFNB - PubMed: Kimberling 2010 Proband - No ophtalmologic examination - - United States - - - - - 1 Anne-Françoise Roux
-/- 42 c.5418C>G r.(?) p.(Asp1806Glu) Cadherin 17 (1745-1851) Unknown - benign g.73544093C>G g.71784336C>G - - CDH23_000200 heterozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs74145660 Germline - - +MnlI;+BslI;-HpyCH4IV;-BmgBI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband F - China - - - - - 1 Anne-Françoise Roux
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