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.

15 entries on 1 page. Showing entries 1 - 15.
Legend   How to query  

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.2263C>T r.(?) p.(His755Tyr) - Unknown - VUS g.73453990C>T g.71694233C>T - - CDH23_000111 - - - - Germline - - - - - DNA SEQ-NG - - - - PubMed: Bell 2011 - - - - - - - - - 1 Global Variome, with Curator vacancy
-?/. - c.2263C>T r.(?) p.(His755Tyr) - Unknown - likely benign g.73453990C>T g.71694233C>T CDH23(NM_001171930.1):c.2263C>T (p.(His755Tyr)), CDH23(NM_022124.5):c.2263C>T (p.H755Y), CDH23(NM_022124.6):c.2263C>T (p.H755Y) - CDH23_000111 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/? 21 c.2263C>T r.(?) p.(His755Tyr) Cadherin 7 (672-784) Parent #2 ACMG likely benign g.73453990C>T g.71694233C>T - - CDH23_000111 heterozygous PubMed: Oshima 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/192 controls -PhoI;-Sau96I;-HaeIII; - - DNA SEQ - - USH1 - PubMed: Oshima 2008 Proband - - United States - - - - - 1 Anne-Françoise Roux
-?/? 21 c.2263C>T r.(?) p.(His755Tyr) Cadherin 7 (672-784) Unknown ACMG likely benign g.73453990C>T g.71694233C>T - - CDH23_000111 heterozygous; Presumably pathogenic PubMed: Bonnet 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/306 controls -PhoI;-Sau96I;-HaeIII; - - DNA SEQ - - USH2 - PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
-?/? 21 c.2263C>T r.(?) p.(His755Tyr) Cadherin 7 (672-784) Maternal (confirmed) ACMG likely benign g.73453990C>T g.71694233C>T - - CDH23_000111 heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 1/878 controls -PhoI;-Sau96I;-HaeIII; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/? 21 c.2263C>T r.(?) p.(His755Tyr) Cadherin 7 (672-784) Parent #2 ACMG likely benign g.73453990C>T g.71694233C>T - - CDH23_000111 heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs181255269 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bonnet 2016 Proband F - Italy - - - - - 1 Crystel Bonnet
-?/. - c.2263C>T r.(?) p.(His755Tyr) - Unknown - likely benign g.73453990C>T g.71694233C>T CDH23(NM_001171930.1):c.2263C>T (p.(His755Tyr)), CDH23(NM_022124.5):c.2263C>T (p.H755Y), CDH23(NM_022124.6):c.2263C>T (p.H755Y) - CDH23_000111 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.2263C>T r.(?) p.(His755Tyr) - Unknown - likely benign g.73453990C>T g.71694233C>T CDH23(NM_001171930.1):c.2263C>T (p.(His755Tyr)), CDH23(NM_022124.5):c.2263C>T (p.H755Y), CDH23(NM_022124.6):c.2263C>T (p.H755Y) - CDH23_000111 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.2263C>T r.(?) p.(His755Tyr) - Unknown - likely benign g.73453990C>T g.71694233C>T CDH23(NM_001171930.1):c.2263C>T (p.(His755Tyr)), CDH23(NM_022124.5):c.2263C>T (p.H755Y), CDH23(NM_022124.6):c.2263C>T (p.H755Y) - CDH23_000111 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.2263C>T r.(?) p.(His755Tyr) - Parent #1 - VUS g.73453990C>T g.71694233C>T - - CDH23_000111 conflicting interpretations of pathogenicity; 37 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs181255269 Germline - 37/2794 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 37 Mohammed Faruq
?/. - c.2263C>T r.(?) p.(His755Tyr) - Both (homozygous) - likely benign g.73453990C>T g.71694233C>T - - CDH23_000111 - Doucette 2021, submitted ClinVar-45891 rs181255269 Germline yes - - - - DNA SEQ-NG - - DFNB, maculopathy M73 II-1 Doucette 2021, submitted single child to unaffected parents (father was unavailable for examination) M yes Canada Middle Eastern - - Yes - 1 Lance P Doucette
-?/. - c.2263C>T r.(?) p.(His755Tyr) - Unknown - likely benign g.73453990C>T - - - CDH23_000111 - - - rs181255269 CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.2263C>T r.(?) p.(His755Tyr) - Both (homozygous) - pathogenic (recessive) g.73453990C>T g.71694233C>T - - CDH23_000111 - PubMed: Zaneveld 2015 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease Pat70 PubMed: Zaneveld 2015 - - - Canada - - - - - 1 LOVD
+?/. - c.2263C>T r.(?) p.(His755Tyr) - Both (homozygous) ACMG likely pathogenic g.73453990C>T g.71694233C>T CDH23 c.2263C>T, p.(His755Tyr), c.2263C>T, p.(His755Tyr) - CDH23_000111 homozygous PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 74 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+?/. - c.2263C>T r.(?) p.(His755Tyr) - Unknown ACMG likely pathogenic g.73453990C>T g.71694233C>T EYS c.2023+5G>T, p.(?), c.2137+1G>A, p.(?), CDH23 c.268C>T, p.(Arg90Trp), c.2263C>T, p.(His755Tyr), c.3221A>T, p.(Asp1074Val) - CDH23_000111 - PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 135 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.