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.

17 entries on 1 page. Showing entries 1 - 17.
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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     
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Parent #1 - benign g.73558952C>T g.71799195C>T - - CDH23_000012 heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Roux 2006 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Unknown - benign g.73558952C>T g.71799195C>T - - CDH23_000012 heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Roux 2006 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Paternal (inferred) - benign g.73558952C>T g.71799195C>T - - CDH23_000012 homozygous PubMed: Ebermann 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - 0/200 controls -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Ebermann 2007 Proband - - Canada - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Maternal (inferred) - benign g.73558952C>T g.71799195C>T - - CDH23_000012 homozygous PubMed: Ebermann 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - 0/200 controls -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Ebermann 2007 Proband - - Canada - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Paternal (inferred) - benign g.73558952C>T g.71799195C>T - - CDH23_000012 homozygous PubMed: Ebermann 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - 0/200 controls -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Ebermann 2007 Proband - - Canada - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Maternal (inferred) - benign g.73558952C>T g.71799195C>T - - CDH23_000012 homozygous PubMed: Ebermann 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - 0/200 controls -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Ebermann 2007 Proband - - Canada - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Parent #1 - benign g.73558952C>T g.71799195C>T - - CDH23_000012 heterozygous PubMed: Ebermann 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - 0/200 controls -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Ebermann 2007 Proband - - Canada - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Unknown - benign g.73558952C>T g.71799195C>T - - CDH23_000012 heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Paternal (inferred) - benign g.73558952C>T g.71799195C>T - - CDH23_000012 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Baux 2008 Proband F - Guinea - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Maternal (inferred) - benign g.73558952C>T g.71799195C>T - - CDH23_000012 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Baux 2008 Proband F - Guinea - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.7139c>u p.Pro2380Leu Cadherin 22 (2297-2402) Unknown - benign g.73558952C>T g.71799195C>T - - CDH23_000012 heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA, RNA RT-PCR, SEQ - - USH1 - PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Paternal (inferred) - benign g.73558952C>T g.71799195C>T - - CDH23_000012 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - Italy - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Maternal (inferred) - benign g.73558952C>T g.71799195C>T - - CDH23_000012 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband M - Italy - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Paternal (inferred) - benign g.73558952C>T g.71799195C>T chr10:g.73558952C>T-c.419C>T-p.P140L in ENST00000224721 - CDH23_000012 homozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband M - China - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Unknown - benign g.73558952C>T g.71799195C>T chr10:g.73558952C>T-c.419C>T-p.P140L in ENST00000224721 - CDH23_000012 homozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Rong 2014 Proband - variants found in samples of two affected brothers. They carry the same causative mutations in MYO7A, but other variants cannot be discriminated from the publication. M - China - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Unknown - benign g.73558952C>T g.71799195C>T chr10:g.73558952C>T-c.419C>T-p.P140L in ENST00000224721 - CDH23_000012 heterozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband F - China - - - - - 1 Anne-Françoise Roux
-/- 51 c.7139C>T r.(?) p.(Pro2380Leu) Cadherin 22 (2297-2402) Maternal (inferred) - benign g.73558952C>T g.71799195C>T chr10:g.73558952C>T-c.419C>T-p.P140L in ENST00000224721 - CDH23_000012 homozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs4747195 Germline - - -FauI;-AciI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband M - China - - - - - 1 Anne-Françoise Roux
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