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.

6 entries on 1 page. Showing entries 1 - 6.
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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     
+?/? 10 c.902G>A r.(?) p.(Arg301Gln) Cadherin 3 (237-348) Parent #1 ACMG VUS g.73375330G>A g.71615573G>A - - CDH23_000125 heterozygous; Possible pathologic PubMed: Wagatsuma 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908355 Germline - 0/292 controls - - - DNA SEQ - - DFNB - PubMed: Wagatsuma 2007 Proband - referenced as patient #2714 in Miyagawa et al., 2012 M - Japan - - - - - 1 Anne-Françoise Roux
+?/? 10 c.902G>A r.(?) p.(Arg301Gln) Cadherin 3 (237-348) Parent #1 ACMG VUS g.73375330G>A g.71615573G>A - - CDH23_000125 heterozygous; Possible pathologic PubMed: Wagatsuma 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908355 Germline - 0/292 controls - - - DNA SEQ - - DFNB - PubMed: Wagatsuma 2007 Proband - referenced as patient #2886 in Miyagawa et al., 2012 M - Japan - - - - - 1 Anne-Françoise Roux
+?/? 10 c.902G>A r.(?) p.(Arg301Gln) Cadherin 3 (237-348) Parent #1 ACMG VUS g.73375330G>A g.71615573G>A - - CDH23_000125 heterozygous; Possible pathologic PubMed: Wagatsuma 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908355 Germline - 0/292 controls - - - DNA SEQ - - DFNB - PubMed: Wagatsuma 2007 Relative - referenced as patient #2885 in Miyagawa et al., 2012 M - Japan - - - - - 1 Anne-Françoise Roux
+?/? 10 c.902G>A r.(?) p.(Arg301Gln) Cadherin 3 (237-348) Parent #2 ACMG VUS g.73375330G>A g.71615573G>A - - CDH23_000125 heterozygous; Possible pathologic PubMed: Miyagawa 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908355 Germline - 1/384 controls - - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Miyagawa 2012 Proband F - Japan - - - - - 1 Anne-Françoise Roux
+?/? 10 c.902G>A r.(?) p.(Arg301Gln) Cadherin 3 (237-348) Unknown ACMG VUS g.73375330G>A g.71615573G>A - - CDH23_000125 heterozygous; Possible pathologic PubMed: Miyagawa 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908355 Germline - 1/384 controls - - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Miyagawa 2012 Proband F - Japan - - - - - 1 Anne-Françoise Roux
+?/? 10 c.902G>A r.(?) p.(Arg301Gln) Cadherin 3 (237-348) Parent #2 ACMG VUS g.73375330G>A g.71615573G>A - - CDH23_000125 heterozygous; Possible pathologic PubMed: Miyagawa 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908355 Germline - 1/384 controls - - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Miyagawa 2012 Relative F - Japan - - - - - 1 Anne-Françoise Roux
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