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.

10 entries on 1 page. Showing entries 1 - 10.
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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     

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Consanguinity     

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VIP     

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Owner     
+?/? 26 c.3016G>A r.(?) p.(Glu1006Lys) Cadherin 10 (996-1102) Unknown ACMG VUS g.73466716G>A g.71706959G>A - - CDH23_000327 heterozygous; Mutation PubMed: Schultz 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls +StyI;-Hpy188I;-MnlI; - - DNA SEQ - - DFNB - PubMed: Schultz 2011 Proband - father M - United States - - - - - 1 Anne-Françoise Roux
+?/? 26 c.3016G>A r.(?) p.(Glu1006Lys) Cadherin 10 (996-1102) Unknown ACMG VUS g.73466716G>A g.71706959G>A - - CDH23_000327 heterozygous; Mutation PubMed: Schultz 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls +StyI;-Hpy188I;-MnlI; - - DNA SEQ - - USH1 - PubMed: Schultz 2011 Proband F - United States - - - - - 1 Anne-Françoise Roux
+?/? 26 c.3016G>A r.(?) p.(Glu1006Lys) Cadherin 10 (996-1102) Paternal (inferred) ACMG VUS g.73466716G>A g.71706959G>A - - CDH23_000327 homozygous PubMed: Schultz 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls +StyI;-Hpy188I;-MnlI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Schultz 2011 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+?/? 26 c.3016G>A r.(?) p.(Glu1006Lys) Cadherin 10 (996-1102) Paternal (confirmed) ACMG VUS g.73466716G>A g.71706959G>A - - CDH23_000327 heterozygous; Mutation PubMed: Schultz 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls +StyI;-Hpy188I;-MnlI; - - DNA SEQ - - USH1 - PubMed: Schultz 2011 Proband - daughter 1 F - United States - - - - - 1 Anne-Françoise Roux
+?/? 26 c.3016G>A r.(?) p.(Glu1006Lys) Cadherin 10 (996-1102) Maternal (inferred) ACMG VUS g.73466716G>A g.71706959G>A - - CDH23_000327 homozygous PubMed: Schultz 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls +StyI;-Hpy188I;-MnlI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Schultz 2011 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+?/. - c.3016G>A r.(?) p.(Glu1006Lys) - Unknown - likely pathogenic g.73466716G>A - - - CDH23_000327 - - - rs745571683 CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. 26 c.3016G>A r.(?) p.(Glu1006Lys) - Unknown - likely pathogenic g.73466716G>A - c.3016G>A - CDH23_000327 - PubMed: Colombo-2020 - rs745571683 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+?/. 26 c.3016G>A r.(?) p.(Glu1006Lys) - Unknown - likely pathogenic g.73466716G>A - c.3016G>A,p.E1006K - CDH23_000327 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 26 c.3016G>A r.(?) p.(Glu1006Lys) - Unknown - likely pathogenic g.73466716G>A - p.E1006K - CDH23_000327 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. - c.3016G>A r.(?) p.(Glu1006Lys) - Unknown ACMG likely pathogenic (recessive) g.73466716G>A g.71706959G>A - - CDH23_000327 ACMG PM2, PP5_STRONG PubMed: Weisschuh 2024 618010 - Germline - - - - - DNA SEQ-NG - WGS ? USHII-365 PubMed: Weisschuh 2024 patient F - Germany - - - - - 1 Johan den Dunnen
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