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.

18 entries on 1 page. Showing entries 1 - 18.
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     
+?/. 47 c.6442G>A r.(?) p.(Asp2148Asn) - Parent #1 - likely pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - Germline - - - - - DNA SEQ-NG - - deafness - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - 1 Mieke Wesdorp
+?/. - c.6442G>A r.(?) p.(Asp2148Asn) - Unknown - likely pathogenic g.73553127G>A g.71793370G>A CDH23(NM_022124.5):c.6442G>A (p.D2148N) - CDH23_000128 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Parent #1 - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 heterozygous PubMed: Astuto 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - - -BsiEI - - DNA SEQ - - DFNB - PubMed: Astuto 2002 Proband - - Germany - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Paternal (inferred) - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 homozygous PubMed: de Brouwer 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - 0/400 controls -BsiEI - - DNA SEQ - - DFNB - PubMed: de Brouwer 2003 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Paternal (inferred) - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 homozygous PubMed: de Brouwer 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - 0/400 controls -BsiEI - - DNA SEQ - - DFNB - PubMed: de Brouwer 2003 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Parent #1 - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 heterozygous PubMed: de Brouwer 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - 0/400 controls -BsiEI - - DNA SEQ - - DFNB - PubMed: de Brouwer 2003 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Parent #1 - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 heterozygous PubMed: de Brouwer 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - 0/400 controls -BsiEI - - DNA SEQ - - DFNB - PubMed: de Brouwer 2003 Relative F - - - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Maternal (inferred) - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 homozygous PubMed: de Brouwer 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - 0/400 controls -BsiEI - - DNA SEQ - - DFNB - PubMed: de Brouwer 2003 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Maternal (inferred) - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 homozygous PubMed: de Brouwer 2003; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - 0/400 controls -BsiEI - - DNA SEQ - - DFNB - PubMed: de Brouwer 2003 Relative M - - - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Paternal (inferred) - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 homozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - - -BsiEI - - DNA SEQ - - DFNB - PubMed: Pennings 2004 Proband M - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Parent #1 - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - - -BsiEI - - DNA SEQ - - DFNB - PubMed: Pennings 2004 Proband F - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Parent #1 - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - - -BsiEI - - DNA SEQ - - DFNB - PubMed: Pennings 2004 Relative F - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Maternal (inferred) - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 homozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - - -BsiEI - - DNA SEQ - - DFNB - PubMed: Pennings 2004 Proband M - Netherlands - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Paternal (confirmed) - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 heterozygous; Mutation PubMed: Schultz 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - - -BsiEI - - DNA SEQ - - DFNB - PubMed: Schultz 2011 Proband M - United States - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Paternal (confirmed) - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 heterozygous; Mutation PubMed: Schultz 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - - -BsiEI - - DNA SEQ - - DFNB - PubMed: Schultz 2011 Relative - intrafamilial phenotypic variability M - United States - - - - - 1 Anne-Françoise Roux
+/+ 48 c.6442G>A r.(?) p.(Asp2148Asn) Cadherin 20 (2070-2174) Parent #2 - pathogenic g.73553127G>A g.71793370G>A - - CDH23_000128 heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033271 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
+?/. - c.6442G>A r.(?) p.(Asp2148Asn) - Unknown - likely pathogenic g.73553127G>A g.71793370G>A CDH23(NM_022124.5):c.6442G>A (p.D2148N) - CDH23_000128 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.6442G>A r.(?) p.(Asp2148Asn) - Both (homozygous) - likely pathogenic (recessive) g.73553127G>A g.71793370G>A - - CDH23_000128 ACMG PM2, PM3, PP1, PP3 PubMed: Khan 2024, Journal: Khan 2024 VCV000004922.42 - Germline - - - - - DNA SEQ, SEQ-NG - WES LIS HLRBS9 PubMed: Khan 2024, Journal: Khan 2024 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes Pakistan - - - - - 1 Hina Khan
Legend   How to query  


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