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.

7 entries on 1 page. Showing entries 1 - 7.
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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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/? 65i c.9319+72_9319+73insTC r.(?) p.(=) - Unknown ACMG likely benign g.73571582_73571583insTC g.71811825_71811826insTC - - CDH23_000176 heterozygous PubMed: Roux 2011 - rs59718926 Germline - - +MnlI;+MwoI;-BstXI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-/? 65i c.9319+72_9319+73insTC r.(?) p.(=) - Paternal (inferred) ACMG likely benign g.73571582_73571583insTC g.71811825_71811826insTC - - CDH23_000176 homozygous PubMed: Roux 2011 - rs59718926 Germline - - +MnlI;+MwoI;-BstXI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - Italy - - - - - 1 Anne-Françoise Roux
-/? 65i c.9319+72_9319+73insTC r.(?) p.(=) - Unknown ACMG likely benign g.73571582_73571583insTC g.71811825_71811826insTC - - CDH23_000176 heterozygous PubMed: Roux 2011 - rs59718926 Germline - - +MnlI;+MwoI;-BstXI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 65i c.9319+72_9319+73insTC r.(?) p.(=) - Maternal (inferred) ACMG likely benign g.73571582_73571583insTC g.71811825_71811826insTC - - CDH23_000176 homozygous PubMed: Roux 2011 - rs59718926 Germline - - +MnlI;+MwoI;-BstXI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - Italy - - - - - 1 Anne-Françoise Roux
-/? 65i c.9319+72_9319+73insTC r.(?) p.(=) - Unknown ACMG likely benign g.73571582_73571583insTC g.71811825_71811826insTC - - CDH23_000176 heterozygous PubMed: Aparis 2013 - rs59718926 Germline - - +MnlI;+MwoI;-BstXI; - - DNA minigene, RT-PCR, SEQ - - USH1 - PubMed: Aparisi 2013 Proband - - Spain - - - - - 1 Jose Maria Millan
-/? 65i c.9319+72_9319+73insTC r.(?) p.(=) - Paternal (inferred) ACMG likely benign g.73571582_73571583insTC g.71811825_71811826insTC - - CDH23_000176 homozygous PubMed: Besnard, Garcia-Garcia 2014 - rs59718926 Germline - - +MnlI;+MwoI;-BstXI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Besnard, Garcia-Garcia 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-/? 65i c.9319+72_9319+73insTC r.(?) p.(=) - Maternal (inferred) ACMG likely benign g.73571582_73571583insTC g.71811825_71811826insTC - - CDH23_000176 homozygous PubMed: Besnard, Garcia-Garcia 2014 - rs59718926 Germline - - +MnlI;+MwoI;-BstXI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Besnard, Garcia-Garcia 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
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