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     

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Re-site     

VIP     

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Tissue     

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Disease     

ID_report     

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VIP     

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Owner     
+?/? 61 c.8903T>C r.(?) p.(Val2968Ala) Cadherin 27 (2847-2975) Unknown ACMG VUS g.73569757T>C g.71810000T>C - - CDH23_000118 heterozygous PubMed: Oshima 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/192 controls - - - DNA SEQ - - USH1 - PubMed: Oshima 2008 Proband - - Spain - - - - - 1 Anne-Françoise Roux
?/. - c.8903T>C r.(?) p.(Val2968Ala) - Unknown - VUS g.73569757T>C - - - CDH23_000118 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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