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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

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Re-site     

VIP     

Methylation     

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Tissue     

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Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
-?/? 13 c.1270G>A r.(?) p.(Val424Met) Cadherin 4 (349-460) Unknown ACMG likely benign g.73405717G>A g.71645960G>A - - CDH23_000411 heterozygous; uncertain PubMed: Mizutari 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs2305207 Germline - 0/190 controls hmutai - - DNA SEQ - - DFN - PubMed: Mizutari 2015 proband M - Japan Asian-Japanese - - - - 1 Hideki Mutai
?/. - c.1270G>A r.(?) p.(Val424Met) - Unknown - VUS g.73405717G>A g.71645960G>A CDH23(NM_022124.5):c.1270G>A (p.V424M) - CDH23_000411 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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