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     
?/. - c.268C>T r.(?) p.(Arg90Trp) - Unknown ACMG VUS g.73269961C>T g.71510204C>T EYS c.2023+5G>T, p.(?), c.2137+1G>A, p.(?), CDH23 c.268C>T, p.(Arg90Trp), c.2263C>T, p.(His755Tyr), c.3221A>T, p.(Asp1074Val) - CDH23_000893 - PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 135 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
?/. - c.268C>T r.(?) p.(Arg90Trp) - Unknown - VUS g.73269961C>T - - - CDH23_000893 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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