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.

8 entries on 1 page. Showing entries 1 - 8.
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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     

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Consanguinity     

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VIP     

Data_av     

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Panel size     

Owner     
+/+ 32 c.4021G>A r.(?) p.(Asp1341Asn) Cadherin 13 (1314-1418) Parent #2 - pathogenic g.73492049G>A g.71732292G>A - - CDH23_000129 heterozygous PubMed: de Brouwer 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908351 Germline - 0/400 controls - - - DNA SEQ - - DFNB - PubMed: de Brouwer 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 32 c.4021G>A r.(?) p.(Asp1341Asn) Cadherin 13 (1314-1418) Parent #2 - pathogenic g.73492049G>A g.71732292G>A - - CDH23_000129 heterozygous PubMed: de Brouwer 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908351 Germline - 0/400 controls - - - DNA SEQ - - DFNB - PubMed: de Brouwer 2003 Relative F - - - - - - - 1 Anne-Françoise Roux
+/+ 32 c.4021G>A r.(?) p.(Asp1341Asn) Cadherin 13 (1314-1418) Parent #2 - pathogenic g.73492049G>A g.71732292G>A - - CDH23_000129 heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908351 Germline - - - - - DNA SEQ - - DFNB - PubMed: Pennings 2004 Proband F - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 32 c.4021G>A r.(?) p.(Asp1341Asn) Cadherin 13 (1314-1418) Parent #2 - pathogenic g.73492049G>A g.71732292G>A - - CDH23_000129 heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908351 Germline - - - - - DNA SEQ - - DFNB - PubMed: Pennings 2004 Relative F - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 32 c.4021G>A r.(?) p.(Asp1341Asn) Cadherin 13 (1314-1418) Parent #1 - pathogenic g.73492049G>A g.71732292G>A - - CDH23_000129 heterozygous PubMed: Jaijo 2010; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908351 Germline - - - - - DNA SEQ - - USH1 - PubMed: Jaijo 2010 Proband - - Spain - - - - - 1 Jose Maria Millan
+/+ 32 c.4021G>A r.(?) p.(Asp1341Asn) Cadherin 13 (1314-1418) Unknown - pathogenic g.73492049G>A g.71732292G>A - - CDH23_000129 heterozygous PubMed: Bujakowska 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs121908351 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bujakowska 2014 Proband - - United States - - - - - 1 Anne-Françoise Roux
?/. - c.4021G>A r.(?) p.(Asp1341Asn) - Unknown - VUS g.73492049G>A g.71732292G>A CDH23(NM_022124.5):c.4021G>A (p.D1341N) - CDH23_000129 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.4021G>A r.(?) p.(Asp1341Asn) - Unknown - pathogenic g.73492049G>A g.71732292G>A CDH23(NM_022124.5):c.4021G>A (p.D1341N) - CDH23_000129 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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