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.

8 entries on 1 page. Showing entries 1 - 8.
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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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/? 50 c.6847G>A r.(?) p.(Val2283Ile) Cadherin 21 (2175-2293) Unknown ACMG likely benign g.73558128G>A g.71798371G>A - - CDH23_000197 heterozygous; Uncertain pathogenicity PubMed: Wagatsuma 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41281334 Germline - 3/280 controls +BtsCI;+FokI;-HpyCH4IV; - - DNA SEQ - - DFNB - PubMed: Wagatsuma 2007 Proband - - Japan - - - - - 1 Anne-Françoise Roux
-/? 50 c.6847G>A r.(?) p.(Val2283Ile) Cadherin 21 (2175-2293) Unknown ACMG likely benign g.73558128G>A g.71798371G>A - - CDH23_000197 heterozygous; Uncertain pathogenicity PubMed: Wagatsuma 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41281334 Germline - 3/280 controls +BtsCI;+FokI;-HpyCH4IV; - - DNA SEQ - - DFNB - PubMed: Wagatsuma 2007 Proband - - Japan - - - - - 1 Anne-Françoise Roux
-/? 50 c.6847G>A r.(?) p.(Val2283Ile) Cadherin 21 (2175-2293) Unknown ACMG likely benign g.73558128G>A g.71798371G>A - - CDH23_000197 heterozygous; Uncertain pathogenicity PubMed: Wagatsuma 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41281334 Germline - 3/280 controls +BtsCI;+FokI;-HpyCH4IV; - - DNA SEQ - - DFNB - PubMed: Wagatsuma 2007 Proband - - Japan - - - - - 1 Anne-Françoise Roux
-/? 50 c.6847G>A r.(?) p.(Val2283Ile) Cadherin 21 (2175-2293) Paternal (inferred) ACMG likely benign g.73558128G>A g.71798371G>A - - CDH23_000197 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41281334 Germline - - +BtsCI;+FokI;-HpyCH4IV; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - Italy - - - - - 1 Anne-Françoise Roux
-/? 50 c.6847G>A r.(?) p.(Val2283Ile) Cadherin 21 (2175-2293) Maternal (inferred) ACMG likely benign g.73558128G>A g.71798371G>A - - CDH23_000197 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41281334 Germline - - +BtsCI;+FokI;-HpyCH4IV; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - Italy - - - - - 1 Anne-Françoise Roux
-/? 50 c.6847G>A r.(?) p.(Val2283Ile) Cadherin 21 (2175-2293) Unknown ACMG likely benign g.73558128G>A g.71798371G>A - - CDH23_000197 heterozygous; considered non-causative PubMed: Woo 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41281334 Germline - 3/128 controls +BtsCI;+FokI;-HpyCH4IV; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Woo 2014 Proband F - Korea, South (Republic) - - - - - 1 Anne-Françoise Roux
-?/. - c.6847G>A r.(?) p.(Val2283Ile) - Parent #1 - likely benign g.73558128G>A g.71798371G>A - - CDH23_000197 169 heterozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs41281334 Germline - 169/2794 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 169 Mohammed Faruq
-?/. - c.6847G>A r.(?) p.(Val2283Ile) - Both (homozygous) - likely benign g.73558128G>A g.71798371G>A - - CDH23_000197 2 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs41281334 Germline - 2/2794 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 2 Mohammed Faruq
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