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.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Reference     

ClinVar ID     

dbSNP ID     

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Disease     

ID_report     

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Owner     
-?/? 27 c.3178C>T r.(?) p.(Arg1060Trp) Cadherin 10 (996-1102) Parent #1 ACMG likely benign g.73468926C>T g.71709169C>T - - CDH23_000164 heterozygous PubMed: Astuto 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +BsrI;+BmrI;-BssKI;-NciI;-StyD4I;-MspI; - - DNA SEQ - - DFNB - PubMed: Astuto 2002 Proband - - - European - - - - 1 Anne-Françoise Roux
-?/? 27 c.3178C>T r.(?) p.(Arg1060Trp) Cadherin 10 (996-1102) Unknown ACMG likely benign g.73468926C>T g.71709169C>T - - CDH23_000164 heterozygous PubMed: Kimberling 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +BsrI;+BmrI;-BssKI;-NciI;-StyD4I;-MspI; - - DNA SEQ - - DFNB - PubMed: Kimberling 2010 Proband - No ophtalmologic examination - - United States - - - - - 1 Anne-Françoise Roux
-?/? 27 c.3178C>T r.(?) p.(Arg1060Trp) Cadherin 10 (996-1102) Paternal (confirmed) ACMG likely benign g.73468926C>T g.71709169C>T - - CDH23_000164 heterozygous; Presumably pathogenic PubMed: Bonnet 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/626 controls +BsrI;+BmrI;-BssKI;-NciI;-StyD4I;-MspI; - - DNA SEQ - - USH1 - PubMed: Bonnet 2011 Proband F - - - - - - - 1 Anne-Françoise Roux
-?/? 27 c.3178C>T r.(?) p.(Arg1060Trp) Cadherin 10 (996-1102) Unknown ACMG likely benign g.73468926C>T g.71709169C>T - - CDH23_000164 heterozygous; non pathogenic PubMed: Vozzi 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +BsrI;+BmrI;-BssKI;-NciI;-StyD4I;-MspI; - - DNA PE, SEQ - APEX USH2 - PubMed: Vozzi 2011 Proband - - Italy - - - - - 1 Anne-Françoise Roux
-?/? 27 c.3178C>T r.(?) p.(Arg1060Trp) Cadherin 10 (996-1102) Unknown ACMG likely benign g.73468926C>T g.71709169C>T - - CDH23_000164 heterozygous PubMed: Bujakowska 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +BsrI;+BmrI;-BssKI;-NciI;-StyD4I;-MspI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bujakowska 2014 Proband - - United States - - - - - 1 Anne-Françoise Roux
-?/. - c.3178C>T r.(?) p.(Arg1060Trp) - Unknown - likely benign g.73468926C>T g.71709169C>T CDH23(NM_022124.5):c.3178C>T (p.R1060W) - CDH23_000164 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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