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.

5 entries on 1 page. Showing entries 1 - 5.
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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     

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Country     

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VIP     

Data_av     

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Panel size     

Owner     
-?/? 68 c.9524G>A r.(?) p.(Arg3175His) Cytoplasmic (3086-3354) Unknown ACMG likely benign g.73572538G>A g.71812781G>A - - CDH23_000161 heterozygous PubMed: Astuto 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs140884994 Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1 - PubMed: Astuto 2002 Proband - - - - - - - - 1 Anne-Françoise Roux
-?/? 68 c.9524G>A r.(?) p.(Arg3175His) Cytoplasmic (3086-3354) Unknown ACMG likely benign g.73572538G>A g.71812781G>A - - CDH23_000161 heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs140884994 Germline - 0/878 controls +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
?/. - c.9524G>A r.(?) p.(Arg3175His) - Unknown - VUS g.73572538G>A g.71812781G>A CDH23(NM_022124.5):c.9524G>A (p.R3175H) - CDH23_000161 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.9524G>A r.(?) p.(Arg3175His) - Parent #1 - VUS g.73572538G>A g.71812781G>A - - CDH23_000161 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs140884994 Germline - 1/2794 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
+?/. - c.9524G>A r.(?) p.(Arg3175His) - Unknown - likely pathogenic g.73572538G>A - CDH23(NM_022124.5):c.9524G>A (p.R3175H) - CDH23_000161 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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