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     
-/? - c.? r.(?) p.(Glu3251Lys) - Paternal (inferred) ACMG likely benign g.? - ENST00000224721:c.442G>A (Gly148Arg) - CDH23_000243 homozygous; UV1 PubMed: Le Quesne Stabej 2012 - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/? - c.? r.(?) p.(Glu3251Lys) - Paternal (inferred) ACMG likely benign g.? - ENST00000224721:c.442G>A (Gly148Arg) - CDH23_000243 homozygous; UV1 PubMed: Le Quesne Stabej 2012 - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/? - c.? r.(?) p.(Glu3251Lys) - Paternal (inferred) ACMG likely benign g.? - ENST00000224721:c.442G>A (Gly148Arg) - CDH23_000243 homozygous; UV1 PubMed: Le Quesne Stabej 2012 - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/? - c.? r.(?) p.(Glu3251Lys) - Maternal (inferred) ACMG likely benign g.? - ENST00000224721:c.442G>A (Gly148Arg) - CDH23_000243 homozygous; UV1 PubMed: Le Quesne Stabej 2012 - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/. 48 c.? r.(?) p.? - Unknown - likely pathogenic g.73553007G>T - c.6322G>T - CDH23_000243 - PubMed: Eisenberger-2013 - - Germline - - - - - DNA SEQ-NG-I, SEQ-NG-R, SEQ blood - retinal disease - PubMed: Eisenberger-2013 - F no Germany - - - - - 1 LOVD
+?/. 2 c.? r.(?) p.? - Both (homozygous) - likely pathogenic g.? - p.E2973* - CDH23_000243 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 2 c.? r.(?) p.? - Unknown - likely pathogenic g.? - p.Q1965* - CDH23_000243 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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