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.

20 entries on 1 page. Showing entries 1 - 20.
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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)     

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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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VIP     

Data_av     

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Panel size     

Owner     
?/. - c.1096G>A r.(?) p.(Ala366Thr) - Unknown - VUS g.73377112G>A g.71617355G>A - - CDH23_000039 - - - - Germline - - - - - DNA SEQ-NG - - - - PubMed: Bell 2011 - - - - - - - - - 1 Global Variome, with Curator vacancy
-?/. - c.1096G>A r.(?) p.(Ala366Thr) - Unknown - likely benign g.73377112G>A g.71617355G>A CDH23(NM_001171930.1):c.1096G>A (p.(Ala366Thr)), CDH23(NM_022124.5):c.1096G>A (p.A366T) - CDH23_000039 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.1096G>A r.(?) p.(Ala366Thr) - Unknown - benign g.73377112G>A g.71617355G>A CDH23(NM_001171930.1):c.1096G>A (p.(Ala366Thr)), CDH23(NM_022124.5):c.1096G>A (p.A366T) - CDH23_000039 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/? 11 c.1096G>A r.(?) p.(Ala366Thr) Cadherin 4 (349-460) Unknown ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous; likely pathologic PubMed: Ouyang 2005; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - 0/200 controls none - - DNA SEQ - - USH1 - PubMed: Ouyang 2005 Proband - - United States - - - - - 1 Anne-Françoise Roux
-?/? 11 c.1096G>A r.(?) p.(Ala366Thr) Cadherin 4 (349-460) Unknown ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous; likely pathologic PubMed: Ouyang 2005; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - 0/200 controls none - - DNA SEQ - - USH1 - PubMed: Ouyang 2005 Proband - - United States - - - - - 1 Anne-Françoise Roux
-?/? 11 c.1096G>A r.(?) p.(Ala366Thr) Cadherin 4 (349-460) Unknown ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous; likely pathologic PubMed: Ouyang 2005; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - 0/200 controls none - - DNA SEQ - - USH1 - PubMed: Ouyang 2005 Proband - - United States - - - - - 1 Anne-Françoise Roux
-?/? 11 c.1096G>A r.(?) p.(Ala366Thr) Cadherin 4 (349-460) Parent #2 ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - - none - - DNA SEQ - - USH1 - PubMed: Roux 2006 Proband M - France - - - - - 1 Anne-Françoise Roux
-?/? 11 c.1096G>A r.(?) p.(Ala366Thr) Cadherin 4 (349-460) Parent #1 ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous; presumed pathogenic PubMed: Oshima 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - 0/192 controls none - - DNA SEQ - - USH1 - PubMed: Oshima 2008 Proband - - United States - - - - - 1 Anne-Françoise Roux
-?/? 11 c.1096G>A r.(?) p.(Ala366Thr) Cadherin 4 (349-460) Parent #1 ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous; Pathological PubMed: Jaijo 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - - none - - DNA SEQ - - USH2 - PubMed: Jaijo 2010 Proband F - Spain - - - - - 1 Jose Maria Millan
-?/? 11 c.1096G>A r.(?) p.(Ala366Thr) Cadherin 4 (349-460) Unknown ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous; mutation PubMed: Kimberling 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - - none - - DNA SEQ - - DFNB - PubMed: Kimberling 2010 Proband - No ophtalmologic examination - - United States - - - - - 1 Anne-Françoise Roux
-?/? 11 c.1096G>A r.(?) p.(Ala366Thr) Cadherin 4 (349-460) Unknown ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous; mutation PubMed: Kimberling 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - - none - - DNA SEQ - - DFNB - PubMed: Kimberling 2010 Proband - No ophtalmologic examination - - United States - - - - - 1 Anne-Françoise Roux
-?/? 11 c.1096G>A r.1096g>a p.Ala366Thr Cadherin 4 (349-460) Unknown ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - - none - - DNA, RNA RT-PCR, SEQ - - USH1 - PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
-?/? 11 c.1096G>A r.(?) p.(Ala366Thr) Cadherin 4 (349-460) Unknown ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - 1/96 controls none - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/? 11 c.1096G>A r.(?) p.(Ala366Thr) Cadherin 4 (349-460) Unknown ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - 1/96 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/? 11 c.1096G>A r.(?) p.(Ala366Thr) Cadherin 4 (349-460) Unknown ACMG likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 heterozygous; UV2 PubMed: Aparisi 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs143282422 Germline - - none - - DNA SEQ - - USH2 - PubMed: Aparisi 2014 Proband M - Spain - - - - - 1 Jose Maria Millan
-?/. - c.1096G>A r.(?) p.(Ala366Thr) - Unknown - likely benign g.73377112G>A g.71617355G>A CDH23(NM_001171930.1):c.1096G>A (p.(Ala366Thr)), CDH23(NM_022124.5):c.1096G>A (p.A366T) - CDH23_000039 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.1096G>A r.(?) p.(Ala366Thr) - Parent #1 - likely benign g.73377112G>A g.71617355G>A - - CDH23_000039 7 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs143282422 Germline - 7/2793 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 7 Mohammed Faruq
?/. - c.1096G>A r.(?) p.(Ala366Thr) - Unknown - VUS g.73377112G>A g.71617355G>A - - CDH23_000039 - PubMed: Bryant 2018 - rs143282422 Germline - - - - - DNA SEQ-NG - WES retinal disease JB42 PubMed: Bryant 2018 - - - United States - - - - - 1 LOVD
?/. - c.1096G>A r.(?) p.(Ala366Thr) - Parent #1 - VUS g.73377112G>A g.71617355G>A - - CDH23_000039 - PubMed: Bryant 2018 - rs143282422 Germline - - - - - DNA SEQ-NG - WES retinal disease JB40 PubMed: Bryant 2018 - - - United States - - - - - 1 LOVD
-?/. - c.1096G>A r.(?) p.(Ala366Thr) - Unknown - likely benign g.73377112G>A - - - CDH23_000039 - - - rs143282422 Unknown - - - - - - - - - - - - - - - - - - - - - - -
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