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.

13 entries on 1 page. Showing entries 1 - 13.
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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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 46 c.6049G>A r.(?) p.(Gly2017Ser) Cadherin 19 (1960-2069) Parent #1 - pathogenic g.73550170G>A g.71790413G>A - - CDH23_000046 heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +BsrI;+TspRI;-SgrAI;-MspI;-HpaII;-BsaWI; - - DNA SEQ - - USH1 - PubMed: Roux 2006 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 46 c.6049G>A r.(?) p.(Gly2017Ser) Cadherin 19 (1960-2069) Parent #1 - pathogenic g.73550170G>A g.71790413G>A - - CDH23_000046 heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +BsrI;+TspRI;-SgrAI;-MspI;-HpaII;-BsaWI; - - DNA SEQ - - USH1 - PubMed: Roux 2006 Relative F - France - - - - - 1 Anne-Françoise Roux
+/+ 46 c.6049G>A r.(?) p.(Gly2017Ser) Cadherin 19 (1960-2069) Parent #2 - pathogenic g.73550170G>A g.71790413G>A - - CDH23_000046 heterozygous PubMed: Oshima 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/192 controls +BsrI;+TspRI;-SgrAI;-MspI;-HpaII;-BsaWI; - - DNA SEQ - - USH1 - PubMed: Oshima 2008 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 46 c.6049G>A r.(?) p.(Gly2017Ser) Cadherin 19 (1960-2069) Unknown - pathogenic g.73550170G>A g.71790413G>A Pathogenic - was shown in the article to affect splicing (p.(Thr1976_Gly2017del)) - CDH23_000046 heterozygous; Exon skipping PubMed: Aparisi 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +BsrI;+TspRI;-SgrAI;-MspI;-HpaII;-BsaWI; - - DNA minigene, RT-PCR, SEQ - - USH1 - PubMed: Aparisi 2013 Proband - - Spain - - - - - 1 Jose Maria Millan
+/+ 46 c.6049G>A r.(?) p.(Gly2017Ser) Cadherin 19 (1960-2069) Paternal (inferred) - pathogenic g.73550170G>A g.71790413G>A - - CDH23_000046 homozygous PubMed: Aparisi 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +BsrI;+TspRI;-SgrAI;-MspI;-HpaII;-BsaWI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 46 c.6049G>A r.(?) p.(Gly2017Ser) Cadherin 19 (1960-2069) Maternal (inferred) - pathogenic g.73550170G>A g.71790413G>A - - CDH23_000046 homozygous PubMed: Aparisi 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +BsrI;+TspRI;-SgrAI;-MspI;-HpaII;-BsaWI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 46 c.6049G>A r.(?) p.(Gly2017Ser) Cadherin 19 (1960-2069) Paternal (inferred) - pathogenic g.73550170G>A g.71790413G>A - - CDH23_000046 homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 46 c.6049G>A r.(?) p.(Gly2017Ser) Cadherin 19 (1960-2069) Maternal (inferred) - pathogenic g.73550170G>A g.71790413G>A - - CDH23_000046 homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. - c.6049G>A r.(?) p.(Gly2017Ser) - Unknown - likely pathogenic g.73550170G>A g.71790413G>A CDH23(NM_022124.6):c.6049G>A (p.G2017S) - CDH23_000046 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.6049G>A r.(?) p.(Gly2017Ser) - Unknown - likely pathogenic g.73550170G>A g.71790413G>A CDH23(NM_022124.6):c.6049G>A (p.G2017S) - CDH23_000046 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.6049G>A r.(?) p.(Gly2017Ser) - Parent #1 - likely pathogenic g.73550170G>A g.71790413G>A - - CDH23_000046 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs183431253 Germline - 1/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
+/. - c.6049G>A r.(?) p.(Gly2017Ser) - Both (homozygous) - pathogenic (recessive) g.73550170G>A g.71790413G>A - - CDH23_000046 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP957 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+/. 46 c.6049G>A r.(?) p.(Gly2017Ser) - Unknown - pathogenic g.73550170G>A - c.6049G>A - CDH23_000046 - PubMed: Colombo-2020 - rs183431253 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
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