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     

Country     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
-?/? 39 c.4858G>A r.(?) p.(Val1620Met) Cadherin 15 (1529-1634) Paternal (inferred) ACMG likely benign g.73537449G>A g.71777692G>A - - CDH23_000365 homozygous; pathogenicity unclear PubMed: Glöcke 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41281330 Germline - - +CviAII;+FatI;+NlaIII;-AleI;-Hpy166II;-PmlI; - - DNA SEQ, SEQ-NG-S - - USH - PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
-?/? 39 c.4858G>A r.(?) p.(Val1620Met) Cadherin 15 (1529-1634) Maternal (inferred) ACMG likely benign g.73537449G>A g.71777692G>A - - CDH23_000365 homozygous; pathogenicity unclear PubMed: Glöcke 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41281330 Germline - - +CviAII;+FatI;+NlaIII;-AleI;-Hpy166II;-PmlI; - - DNA SEQ, SEQ-NG-S - - USH - PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
-/. - c.4858G>A r.(?) p.(Val1620Met) - Unknown - benign g.73537449G>A g.71777692G>A CDH23(NM_022124.5):c.4858G>A (p.V1620M) - CDH23_000365 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.4858G>A r.(?) p.(Val1620Met) - Parent #1 - benign g.73537449G>A g.71777692G>A - - CDH23_000365 200 heterozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs41281330 Germline - 200/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 200 Mohammed Faruq
-/. - c.4858G>A r.(?) p.(Val1620Met) - Both (homozygous) - benign g.73537449G>A g.71777692G>A - - CDH23_000365 4 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs41281330 Germline - 4/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 4 Mohammed Faruq
?/. - c.4858G>A r.(?) p.(Val1620Met) - Unknown - VUS g.73537449G>A g.71777692G>A - - CDH23_000365 - PubMed: Eandi 2017 - - Germline - - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam6PatTO7 PubMed: Eandi 2017 - F - Italy - - - - - 1 LOVD
?/. - c.4858G>A r.(?) p.(Val1620Met) - Unknown - VUS g.73537449G>A g.71777692G>A - - CDH23_000365 - PubMed: Eandi 2017 - - Germline yes - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam11PatTO14 PubMed: Eandi 2017 - M - Italy - - - - - 1 LOVD
+?/. - c.4858G>A r.(?) p.(Val1620Met) - Parent #1 - likely pathogenic g.73537449G>A g.71777692G>A CDH23, variant 1: c.4858G>A/p.V1620M, variant 2: c.4858G>A/p.V1620M - CDH23_000365 solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET2 targeted sequencing panel - see paper retinal disease 400 PubMed: Weisschuh 2020 Filing key number: 130, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
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