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.

9 entries on 1 page. Showing entries 1 - 9.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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DB-ID     

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ClinVar ID     

dbSNP ID     

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Disease     

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Owner     
-/- 15 c.1487G>A r.(?) p.(Ser496Asn) Cadherin 5 (461-561) Parent #1 - benign g.73434906G>A g.71675149G>A - - CDH23_000049 heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10999947 Germline - - +HincII;+Hpy166II;-AluI;-CviKI_1 - - DNA SEQ - - USH1 - PubMed: Roux 2006 Relative F - France - - - - - 1 Anne-Françoise Roux
-/- 15 c.1487G>A r.(?) p.(Ser496Asn) Cadherin 5 (461-561) Unknown - benign g.73434906G>A g.71675149G>A - - CDH23_000049 heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10999947 Germline - - +HincII;+Hpy166II;-AluI;-CviKI_1 - - DNA SEQ - - USH1 - PubMed: Roux 2006 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 15 c.1487G>A r.1487g>a p.Ser496Asn Cadherin 5 (461-561) Unknown - benign g.73434906G>A g.71675149G>A - - CDH23_000049 heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10999947 Germline - - +HincII;+Hpy166II;-AluI;-CviKI_1 - - DNA, RNA RT-PCR, SEQ - - USH1 - PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 15 c.1487G>A r.(?) p.(Ser496Asn) Cadherin 5 (461-561) Paternal (inferred) - benign g.73434906G>A g.71675149G>A - - CDH23_000049 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10999947 Germline - - +HincII;+Hpy166II;-AluI;-CviKI_1 - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 15 c.1487G>A r.(?) p.(Ser496Asn) Cadherin 5 (461-561) Maternal (inferred) - benign g.73434906G>A g.71675149G>A - - CDH23_000049 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10999947 Germline - - +HincII;+Hpy166II;-AluI;-CviKI_1 - - DNA SEQ - - USH1 - PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 15 c.1487G>A r.(?) p.(Ser496Asn) Cadherin 5 (461-561) Paternal (inferred) - benign g.73434906G>A g.71675149G>A - - CDH23_000049 homozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10999947 Germline - - +HincII;+Hpy166II;-AluI;-CviKI_1 - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 15 c.1487G>A r.(?) p.(Ser496Asn) Cadherin 5 (461-561) Maternal (inferred) - benign g.73434906G>A g.71675149G>A - - CDH23_000049 homozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10999947 Germline - - +HincII;+Hpy166II;-AluI;-CviKI_1 - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 15 c.1487G>A r.(?) p.(Ser496Asn) Cadherin 5 (461-561) Unknown - benign g.73434906G>A g.71675149G>A - - CDH23_000049 heterozygous PubMed: Aparis 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10999947 Germline - - +HincII;+Hpy166II;-AluI;-CviKI_1 - - DNA minigene, RT-PCR, SEQ - - USH1 - PubMed: Aparisi 2013 Proband - - Spain - - - - - 1 Jose Maria Millan
-/- 15 c.1487G>A r.(?) p.(Ser496Asn) Cadherin 5 (461-561) Unknown - benign g.73434906G>A g.71675149G>A - - CDH23_000049 heterozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10999947 Germline - - +HincII;+Hpy166II;-AluI;-CviKI_1 - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband M - China - - - - - 1 Anne-Françoise Roux
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