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.

2 entries on 1 page. Showing entries 1 - 2.
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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     
-/- 2 c.7C>T r.(?) p.(Arg3Cys) Signal peptide (1-23) Paternal (inferred) - benign g.73199595C>T g.71439838C>T - - CDH23_000094 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs7902757 Germline - - - - - DNA SEQ - - USH1 - PubMed: Baux 2008 Proband F - Guinea - - - - - 1 Anne-Françoise Roux
-/- 2 c.7C>T r.(?) p.(Arg3Cys) Signal peptide (1-23) Maternal (inferred) - benign g.73199595C>T g.71439838C>T - - CDH23_000094 homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs7902757 Germline - - - - - DNA SEQ - - USH1 - PubMed: Baux 2008 Proband F - Guinea - - - - - 1 Anne-Françoise Roux
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