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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/? 53 c.7466G>A r.(?) p.(Arg2489His) Cadherin 23 (2403-2509) Unknown ACMG VUS g.73560496G>A g.71800739G>A - - CDH23_000346 heterozygous; Uncertain pathogenicity PubMed: Wagatsuma 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs141986620 Germline - 0/292 controls + Tsp45I;-BstUI;-Hpy99I;-MwoI,;-NruI; - - DNA SEQ - - DFNB - PubMed: Wagatsuma 2007 Proband - - Japan - - - - - 1 Anne-Françoise Roux
?/. - c.7466G>A r.(?) p.(Arg2489His) - Unknown - VUS g.73560496G>A g.71800739G>A CDH23(NM_022124.6):c.7466G>A (p.R2489H) - CDH23_000346 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.7466G>A r.(?) p.(Arg2489His) - Parent #1 - pathogenic g.73560496G>A g.71800739G>A - - CDH23_000346 - PubMed: Zhao 2015 - - Germline - - - - - DNA SEQ-NG - 86-gene panel retinal disease Rp399A PubMed: Zhao 2015 simplex case - - Northern Ireland - - - - - 1 LOVD
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