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.

21 entries on 1 page. Showing entries 1 - 21.
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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     
+/. 54 c.7903G>T r.(?) p.(Val2635Phe) - Both (homozygous) - pathogenic g.73565593G>T g.71805836G>T - - CDH23_000337 not in 106 hearing controls PubMed: Brownstein 2011, Journal: Brownstein 2011 - - Germline yes 2/133 cases (hom), 1/133 cases (het) - - - DNA SEQ-NG-I blood - DFNB12 - PubMed: Brownstein 2011, Journal: Brownstein 2011 3-generation family, 9 affecteds (4F, 5M), unaffected heterozygous carrier parents/sibs F;M no Israel Algeria;Jewish - - - - 9 Zippi Brownstein
+/. 54 c.7903G>T r.(?) p.(Val2635Phe) - Both (homozygous) - pathogenic g.73565593G>T g.71805836G>T - - CDH23_000337 not in 133 controls PubMed: Brownstein 2011, Journal: Brownstein 2011 - - Germline yes 2/133 cases (hom), 1/133 cases (het) - - - DNA SEQ-NG-I blood - DFNB12 - PubMed: Brownstein 2011, Journal: Brownstein 2011 2-generation family, affected brother/sister, unaffected heterozygous carrier parents/sib F;M yes Israel Algeria;Jewish - - - - 2 Zippi Brownstein
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Paternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Proband F - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Paternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative M - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Paternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative M - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Paternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 - F - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Paternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative M - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Paternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative F - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Paternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative M - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Paternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative M - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Paternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative F - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Maternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Proband F - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Maternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative M - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Maternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative M - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Maternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 - F - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Maternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative M - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Maternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative F - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Maternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative M - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Maternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative M - Israel - - - - - 1 Anne-Françoise Roux
+?/? 56 c.7903G>T r.(?) p.(Val2635Phe) Cadherin 25 (2614-2722) Maternal (inferred) ACMG VUS g.73565593G>T g.71805836G>T - - CDH23_000337 homozygous; Pathogenic PubMed: Brownstein 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/106 controls -Hpy166II;-MnlI;-AccI; - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein 2011 Relative F - Israel - - - - - 1 Anne-Françoise Roux
?/. - c.7903G>T r.(?) p.(Val2635Phe) - Unknown - VUS g.73565593G>T - - - CDH23_000337 - - - rs763721044 CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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