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.

12 entries on 1 page. Showing entries 1 - 12.
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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     
+/+ 37 c.4504C>T r.(?) p.(Arg1502*) Cadherin 14 (1420-1527) Paternal (inferred) - pathogenic g.73500594C>T g.71740837C>T - - CDH23_000149 homozygous PubMed: Astuto 2002 - - Germline - - - - - DNA SEQ - - USH - PubMed: Astuto 2002 Proband - - Sweden - - - - - 1 Anne-Françoise Roux
+/+ 37 c.4504C>T r.(?) p.(Arg1502*) Cadherin 14 (1420-1527) Paternal (inferred) - pathogenic g.73500594C>T g.71740837C>T - - CDH23_000149 homozygous PubMed: Astuto 2002 - - Germline - - - - - DNA SEQ - - USH - PubMed: Astuto 2002 Relative - - Sweden - - - - - 1 Anne-Françoise Roux
+/+ 37 c.4504C>T r.(?) p.(Arg1502*) Cadherin 14 (1420-1527) Unknown - pathogenic g.73500594C>T g.71740837C>T - - CDH23_000149 heterozygous PubMed: Astuto 2002 - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Astuto 2002 Proband - - Sweden - - - - - 1 Anne-Françoise Roux
+/+ 37 c.4504C>T r.(?) p.(Arg1502*) Cadherin 14 (1420-1527) Maternal (inferred) - pathogenic g.73500594C>T g.71740837C>T - - CDH23_000149 homozygous PubMed: Astuto 2002 - - Germline - - - - - DNA SEQ - - USH - PubMed: Astuto 2002 Proband - - Sweden - - - - - 1 Anne-Françoise Roux
+/+ 37 c.4504C>T r.(?) p.(Arg1502*) Cadherin 14 (1420-1527) Maternal (inferred) - pathogenic g.73500594C>T g.71740837C>T - - CDH23_000149 homozygous PubMed: Astuto 2002 - - Germline - - - - - DNA SEQ - - USH - PubMed: Astuto 2002 Relative - - Sweden - - - - - 1 Anne-Françoise Roux
+/+ 37 c.4504C>T r.(?) p.(Arg1502*) Cadherin 14 (1420-1527) Parent #2 - pathogenic g.73500594C>T g.71740837C>T - - CDH23_000149 heterozygous PubMed: Astuto 2002 - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Astuto 2002 Proband - - Sweden - - - - - 1 Anne-Françoise Roux
+/+ 37 c.4504C>T r.(?) p.(Arg1502*) Cadherin 14 (1420-1527) Parent #2 - pathogenic g.73500594C>T g.71740837C>T - - CDH23_000149 heterozygous PubMed: Astuto 2002 - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Astuto 2002 Relative - - Sweden - - - - - 1 Anne-Françoise Roux
+/+ 37 c.4504C>T r.(?) p.(Arg1502*) Cadherin 14 (1420-1527) Parent #2 - pathogenic g.73500594C>T g.71740837C>T - - CDH23_000149 heterozygous PubMed: Astuto 2002 - - Germline - - - - - DNA SEQ - - USH - PubMed: Astuto 2002 Proband - - Sweden - - - - - 1 Anne-Françoise Roux
+/+ 37 c.4504C>T r.(?) p.(Arg1502*) Cadherin 14 (1420-1527) Parent #2 - pathogenic g.73500594C>T g.71740837C>T - - CDH23_000149 heterozygous PubMed: Astuto 2002 - - Germline - - - - - DNA SEQ - - USH - PubMed: Astuto 2002 Relative - - Sweden - - - - - 1 Anne-Françoise Roux
+/. 37 c.4504C>T r.(?) p.(Arg1502*) Cadherin 14 (1420-1527) Parent #1 - pathogenic g.73500594C>T - - - CDH23_000149 heterozygous PubMed: Ivanova 2018 - - Germline - - - - - DNA SEQ-NG-S - - USH1 Pat26 PubMed: Ivanova 2018 Proband F - Russian Federation Slavonian - - - - 1 Vladimir Strelnikov
+?/. - c.4504C>T r.(?) p.(Arg1502*) - Unknown ACMG likely pathogenic g.73500594C>T g.71740837C>T CDH23 c.4504C>T, p.(Arg1502*) - CDH23_000149 single heterozygous variant (recessive) PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 369 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+/. 37 c.4504C>T r.(?) p.(Arg1502*) - Unknown - pathogenic g.73500594C>T - c.4504C>T - CDH23_000149 - PubMed: Colombo-2020 - rs769742202 Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
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