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.

13 entries on 1 page. Showing entries 1 - 13.
Legend   How to query  

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     
-/- 47 c.6130G>A r.(?) p.(Glu2044Lys) Cadherin 19 (1960-2069) Parent #1 - benign g.73550969G>A g.71791212G>A - - CDH23_000024 heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA SEQ - - USH1 - PubMed: Roux 2006 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.(?) p.(Glu2044Lys) Cadherin 19 (1960-2069) Unknown - benign g.73550969G>A g.71791212G>A - - CDH23_000024 heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA SEQ - - USH1 - PubMed: Roux 2006 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.6130g>a p.Glu2044Lys Cadherin 19 (1960-2069) Unknown - benign g.73550969G>A g.71791212G>A - - CDH23_000024 heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA, RNA RT-PCR, SEQ - - USH1 - PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.(?) p.(Glu2044Lys) Cadherin 19 (1960-2069) Unknown - benign g.73550969G>A g.71791212G>A - - CDH23_000024 heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.(?) p.(Glu2044Lys) Cadherin 19 (1960-2069) Paternal (inferred) - benign g.73550969G>A g.71791212G>A - - CDH23_000024 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA SEQ - - USH1 - PubMed: Baux 2008 Proband F - Guinea - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.(?) p.(Glu2044Lys) Cadherin 19 (1960-2069) Maternal (inferred) - benign g.73550969G>A g.71791212G>A - - CDH23_000024 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA SEQ - - USH1 - PubMed: Baux 2008 Proband F - Guinea - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.6130g>a p.Glu2044Lys Cadherin 19 (1960-2069) Unknown - benign g.73550969G>A g.71791212G>A - - CDH23_000024 heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA, RNA RT-PCR, SEQ - - USH1 - PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.(?) p.(Glu2044Lys) Cadherin 19 (1960-2069) Paternal (inferred) - benign g.73550969G>A g.71791212G>A - - CDH23_000024 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - Italy - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.(?) p.(Glu2044Lys) Cadherin 19 (1960-2069) Maternal (inferred) - benign g.73550969G>A g.71791212G>A - - CDH23_000024 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - Italy - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.(?) p.(Glu2044Lys) Cadherin 19 (1960-2069) Unknown - benign g.73550969G>A g.71791212G>A - - CDH23_000024 heterozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Rong 2014 Proband - variants found in samples of two affected brothers. They carry the same causative mutations in MYO7A, but other variants cannot be discriminated from the publication. M - China - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.(?) p.(Glu2044Lys) Cadherin 19 (1960-2069) Unknown - benign g.73550969G>A g.71791212G>A - - CDH23_000024 heterozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband F - China - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.(?) p.(Glu2044Lys) Cadherin 19 (1960-2069) Paternal (inferred) - benign g.73550969G>A g.71791212G>A - - CDH23_000024 homozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband M - China - - - - - 1 Anne-Françoise Roux
-/- 47 c.6130G>A r.(?) p.(Glu2044Lys) Cadherin 19 (1960-2069) Maternal (inferred) - benign g.73550969G>A g.71791212G>A - - CDH23_000024 homozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10466026 Germline - - -MnlI;-BbvCI;-BspCNI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband M - China - - - - - 1 Anne-Françoise Roux
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.