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     

Consanguinity     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/- 32 c.3845A>G r.(?) p.(Asn1282Ser) Cadherin 12 (1210-1313) Unknown - benign g.73491873A>G g.71732116A>G - - CDH23_000226 heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs149073355 Germline - 8/862 controls none - - DNA SEQ - - USH3 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 32 c.3845A>G r.(?) p.(Asn1282Ser) Cadherin 12 (1210-1313) Unknown - benign g.73491873A>G g.71732116A>G - - CDH23_000226 heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs149073355 Germline - 8/862 controls none - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/. - c.3845A>G r.(?) p.(Asn1282Ser) - Unknown - likely benign g.73491873A>G g.71732116A>G CDH23(NM_001171930.1):c.3845A>G (p.(Asn1282Ser)) - CDH23_000226 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.3845A>G r.(?) p.(Asn1282Ser) - Unknown - likely benign g.73491873A>G g.71732116A>G CDH23(NM_001171930.1):c.3845A>G (p.(Asn1282Ser)) - CDH23_000226 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.3845A>G r.(?) p.(Asn1282Ser) - Unknown - VUS g.73491873A>G g.71732116A>G - - CDH23_000226 - PubMed: Tiwari 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease Case30806 PubMed: Tiwari 2016 see paper F - Switzerland - - - - - 1 LOVD
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