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.

7 entries on 1 page. Showing entries 1 - 7.
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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     
+/+ 50 c.6933del r.(?) p.(Thr2313Profs*60) Cadherin 22 (2297-2402) Paternal (inferred) - pathogenic g.73558214del g.71798457del - - CDH23_000006 homozygous PubMed: von Brederlow 2002 - - Germline - 0/100 controls - - - DNA SEQ - - USH1 - PubMed: von Brederlow 2002 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 50 c.6933del r.(?) p.(Thr2313Profs*60) Cadherin 22 (2297-2402) Paternal (inferred) - pathogenic g.73558214del g.71798457del - - CDH23_000006 homozygous PubMed: von Brederlow 2002 - - Germline - 0/100 controls - - - DNA SEQ - - USH1 - PubMed: von Brederlow 2002 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 50 c.6933del r.(?) p.(Thr2313Profs*60) Cadherin 22 (2297-2402) Paternal (inferred) - pathogenic g.73558214del g.71798457del - - CDH23_000006 homozygous PubMed: von Brederlow 2002 - - Germline - 0/100 controls - - - DNA SEQ - - USH1 - PubMed: von Brederlow 2002 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 50 c.6933del r.(?) p.(Thr2313Profs*60) Cadherin 22 (2297-2402) Maternal (inferred) - pathogenic g.73558214del g.71798457del - - CDH23_000006 homozygous PubMed: von Brederlow 2002 - - Germline - 0/100 controls - - - DNA SEQ - - USH1 - PubMed: von Brederlow 2002 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 50 c.6933del r.(?) p.(Thr2313Profs*60) Cadherin 22 (2297-2402) Maternal (inferred) - pathogenic g.73558214del g.71798457del - - CDH23_000006 homozygous PubMed: von Brederlow 2002 - - Germline - 0/100 controls - - - DNA SEQ - - USH1 - PubMed: von Brederlow 2002 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 50 c.6933del r.(?) p.(Thr2313Profs*60) Cadherin 22 (2297-2402) Maternal (inferred) - pathogenic g.73558214del g.71798457del - - CDH23_000006 homozygous PubMed: von Brederlow 2002 - - Germline - 0/100 controls - - - DNA SEQ - - USH1 - PubMed: von Brederlow 2002 Relative M - - - - - - - 1 Anne-Françoise Roux
+?/. 50 c.6933del r.(?) p.(Thr2313Profs*60) - Unknown - likely pathogenic g.73558214del - c.6933delT, p.T2313Pfs*60 - CDH23_000006 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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