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.

3 entries on 1 page. Showing entries 1 - 3.
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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     
+/+ 27 c.3220G>A r.(?) p.(Asp1074Asn) Cadherin 10 (996-1102) Parent #2 - pathogenic g.73468968G>A g.71709211G>A - - CDH23_000061 heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs750452808 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
-/- 27i c.3220+26A>G r.(=) p.(=) - Paternal (inferred) - benign g.73468994A>G g.71709237A>G - - CDH23_000061 homozygous PubMed: Roux 2011 - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Baux 2008 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 27i c.3220+26A>G r.(=) p.(=) - Maternal (inferred) - benign g.73468994A>G g.71709237A>G - - CDH23_000061 homozygous PubMed: Roux 2011 - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Baux 2008 Proband F - France - - - - - 1 Anne-Françoise Roux
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