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.
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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     
+/+ 36 c.4488G>C r.(?) p.(Gln1496His) Cadherin 14 (1420-1527) Paternal (inferred) - pathogenic g.73499529G>C g.71739772G>C - - CDH23_000003 homozygous PubMed: Bolz 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls - - - DNA SEQ - - USH1 - PubMed: Bolz 2001 Proband M - Cuba - - - - - 1 Anne-Françoise Roux
+/+ 36 c.4488G>C r.(?) p.(Gln1496His) Cadherin 14 (1420-1527) Paternal (inferred) - pathogenic g.73499529G>C g.71739772G>C - - CDH23_000003 homozygous PubMed: Bolz 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls - - - DNA SEQ - - USH1 - PubMed: Bolz 2001 Relative M - Cuba - - - - - 1 Anne-Françoise Roux
+/+ 36 c.4488G>C r.(?) p.(Gln1496His) Cadherin 14 (1420-1527) Paternal (inferred) - pathogenic g.73499529G>C g.71739772G>C - - CDH23_000003 homozygous PubMed: Bolz 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls - - - DNA SEQ - - USH1 - PubMed: Bolz 2001 Relative F - Cuba - - - - - 1 Anne-Françoise Roux
+/+ 36 c.4488G>C r.(?) p.(Gln1496His) Cadherin 14 (1420-1527) Parent #1 - pathogenic g.73499529G>C g.71739772G>C - - CDH23_000003 heterozygous PubMed: Bolz 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls - - - DNA SEQ - - USH1 - PubMed: Bolz 2001 Proband M - Cuba - - - - - 1 Anne-Françoise Roux
+/+ 36 c.4488G>C r.(?) p.(Gln1496His) Cadherin 14 (1420-1527) Parent #1 - pathogenic g.73499529G>C g.71739772G>C - - CDH23_000003 heterozygous PubMed: Bolz 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls - - - DNA SEQ - - USH1 - PubMed: Bolz 2001 Relative F - Cuba - - - - - 1 Anne-Françoise Roux
+/+ 36 c.4488G>C r.(?) p.(Gln1496His) Cadherin 14 (1420-1527) Maternal (inferred) - pathogenic g.73499529G>C g.71739772G>C - - CDH23_000003 homozygous PubMed: Bolz 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls - - - DNA SEQ - - USH1 - PubMed: Bolz 2001 Proband M - Cuba - - - - - 1 Anne-Françoise Roux
+/+ 36 c.4488G>C r.(?) p.(Gln1496His) Cadherin 14 (1420-1527) Maternal (inferred) - pathogenic g.73499529G>C g.71739772G>C - - CDH23_000003 homozygous PubMed: Bolz 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls - - - DNA SEQ - - USH1 - PubMed: Bolz 2001 Relative M - Cuba - - - - - 1 Anne-Françoise Roux
+/+ 36 c.4488G>C r.(?) p.(Gln1496His) Cadherin 14 (1420-1527) Maternal (inferred) - pathogenic g.73499529G>C g.71739772G>C - - CDH23_000003 homozygous PubMed: Bolz 2001; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/400 controls - - - DNA SEQ - - USH1 - PubMed: Bolz 2001 Relative F - Cuba - - - - - 1 Anne-Françoise Roux
+/+ 36 c.4488G>C r.(?) p.(Gln1496His) Cadherin 14 (1420-1527) Parent #1 - pathogenic g.73499529G>C g.71739772G>C - - CDH23_000003 heterozygous PubMed: Astuto 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Astuto 2002 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 36 c.4488G>C r.(?) p.(Gln1496His) Cadherin 14 (1420-1527) Parent #1 - pathogenic g.73499529G>C g.71739772G>C - - CDH23_000003 heterozygous PubMed: Astuto 2002; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1 - PubMed: Astuto 2002 Relative - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 36 c.4488G>C r.(?) p.(Gln1496His) Cadherin 14 (1420-1527) Parent #1 - pathogenic g.73499529G>C g.71739772G>C - - CDH23_000003 heterozygous PubMed: Oshima 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/192 controls - - - DNA SEQ - - USH1 - PubMed: Oshima 2008 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/. - c.4488G>C r.spl p.? - Parent #1 - pathogenic (recessive) g.73499529G>C - - - CDH23_000003 - PubMed: Santana 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - 14 gene panel USH FamUS-4 PubMed: Santana 2019 3-generation family, 2 affected 2M), unaffected parents - - Cuba white - - - - 2 Global Variome, with Curator vacancy
+/. - c.4488G>C r.spl p.? - Both (homozygous) - pathogenic (recessive) g.73499529G>C - - - CDH23_000003 - PubMed: Santana 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - 14 gene panel USH FamUS-5 PubMed: Santana 2019 3-generation family, 2 affected (F), unaffected parents F - Cuba white - - - - 1 Global Variome, with Curator vacancy
+/. - c.4488G>C r.spl p.? - Both (homozygous) - pathogenic (recessive) g.73499529G>C - - - CDH23_000003 - PubMed: Santana 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - 14 gene panel USH FamUS-6 PubMed: Santana 2019 2-generation family, 2 affected (F, M), unaffected parents - yes Cuba white - - - - 2 Global Variome, with Curator vacancy
+/. - c.4488G>C r.spl p.? - Parent #1 - pathogenic (recessive) g.73499529G>C - - - CDH23_000003 - PubMed: Santana 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - 14 gene panel USH FamUS-7 PubMed: Santana 2019 2-generation family, 1 affected (F), unaffected parents F - Cuba white - - - - 1 Global Variome, with Curator vacancy
+/. - c.4488G>C r.spl p.? - Both (homozygous) - pathogenic (recessive) g.73499529G>C - - - CDH23_000003 - PubMed: Santana 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - 14 gene panel USH FamUS-11 PubMed: Santana 2019 2-generation family, 1 affected (F), unaffected parents F - Cuba white - - - - 1 Global Variome, with Curator vacancy
+/. - c.4488G>C r.(?) p.(Gln1496His) - Parent #2 - pathogenic (recessive) g.73499529G>C g.71739772G>C - - CDH23_000003 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP2019t PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+/. 36 c.4488G>C r.(?) p.(Gln1496His) - Unknown - pathogenic g.73499529G>C - c.4488G>C - CDH23_000003 - PubMed: Colombo-2020 - rs121908347 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
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