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.

6 entries on 1 page. Showing entries 1 - 6.
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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     
-?/? 13 c.1282G>A r.(?) p.(Asp428Asn) Cadherin 4 (349-460) Unknown ACMG likely benign g.73405729G>A g.71645972G>A - - CDH23_000412 heterozygous; potential pathogenicity PubMed: Woo 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs188376296 Germline - 2/128 controls - - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Woo 2014 Proband F - Korea, South (Republic) - - - - - 1 Anne-Françoise Roux
-?/? 13 c.1282G>A r.(?) p.(Asp428Asn) Cadherin 4 (349-460) Paternal (inferred) ACMG likely benign g.73405729G>A g.71645972G>A - - CDH23_000412 heterozygous; uncertain PubMed: Mizutari 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs188376296 Germline - 0/190 controls hmutai - - DNA SEQ - - DFN - PubMed: Mizutari 2015 Proband M - Japan Asian-Japanese - - - - 1 Hideki Mutai
-?/? 13 c.1282G>A r.(?) p.(Asp428Asn) Cadherin 4 (349-460) Unknown ACMG likely benign g.73405729G>A g.71645972G>A - - CDH23_000412 heterozygous; uncertain PubMed: Mizutari 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs188376296 Germline - 0/190 controls hmutai - - DNA SEQ - - DFN - PubMed: Mizutari 2015 Proband M - Japan Asian-Japanese - - - - 1 Hideki Mutai
+?/. - c.1282G>A r.(?) p.(Asp428Asn) - Parent #1 ACMG likely pathogenic g.73405729G>A g.71645972G>A - - CDH23_000412 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19691 PubMed: Sun 2018 family - no China - - - - - 1 LOVD
?/. 12 c.1282G>A r.(?) p.(Asp428Asn) - Unknown - VUS g.73405729G>A g.71645972G>A G1282A - CDH23_000412 - PubMed: Katagiri 2014 - rs188376296 Germline - - - - - DNA SEQ-NG - WES retinal disease RP#006 PubMed: Katagiri 2014 family - - Japan - - - - - 1 LOVD
?/. - c.1282G>A r.(?) p.(Asp428Asn) - Unknown - VUS g.73405729G>A - CDH23(NM_001171930.1):c.1282G>A (p.(Asp428Asn)), CDH23(NM_022124.5):c.1282G>A (p.D428N) - CDH23_000412 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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