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.

8 entries on 1 page. Showing entries 1 - 8.
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.3293A>G r.(?) p.(Asn1098Ser) - Unknown - VUS g.73472494A>G g.71712737A>G - - CDH23_000034 - - - - Germline - - - - - DNA SEQ-NG - - - - PubMed: Bell 2011 - - - - - - - - - 1 Global Variome, with Curator vacancy
-?/. - c.3293A>G r.(?) p.(Asn1098Ser) - Unknown - likely benign g.73472494A>G g.71712737A>G CDH23(NM_001171930.1):c.3293A>G (p.(Asn1098Ser)), CDH23(NM_022124.5):c.3293A>G (p.N1098S), CDH23(NM_022124.6):c.3293A>G (p.N1098S) - CDH23_000034 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.3293A>G r.(?) p.(Asn1098Ser) - Unknown - likely benign g.73472494A>G g.71712737A>G CDH23(NM_001171930.1):c.3293A>G (p.(Asn1098Ser)), CDH23(NM_022124.5):c.3293A>G (p.N1098S), CDH23(NM_022124.6):c.3293A>G (p.N1098S) - CDH23_000034 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/? 28 c.3293A>G r.(?) p.(Asn1098Ser) Cadherin 10 (996-1102) Parent #2 ACMG likely benign g.73472494A>G g.71712737A>G - - CDH23_000034 heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41281310 Germline - - - - - DNA SEQ - - USH1 - PubMed: Roux 2006 Proband M - France - - - - - 1 Anne-Françoise Roux
-?/? 28 c.3293A>G r.(?) p.(Asn1098Ser) Cadherin 10 (996-1102) Parent #2 ACMG likely benign g.73472494A>G g.71712737A>G - - CDH23_000034 heterozygous PubMed: Oshima 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41281310 Germline - 0/192 controls - - - DNA SEQ - - USH1 - PubMed: Oshima 2008 Proband - - United States - - - - - 1 Anne-Françoise Roux
-?/. - c.3293A>G r.(?) p.(Asn1098Ser) - Unknown - likely benign g.73472494A>G g.71712737A>G CDH23(NM_001171930.1):c.3293A>G (p.(Asn1098Ser)), CDH23(NM_022124.5):c.3293A>G (p.N1098S), CDH23(NM_022124.6):c.3293A>G (p.N1098S) - CDH23_000034 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.3293A>G r.(?) p.(Asn1098Ser) - Unknown - likely benign g.73472494A>G g.71712737A>G CDH23(NM_001171930.1):c.3293A>G (p.(Asn1098Ser)), CDH23(NM_022124.5):c.3293A>G (p.N1098S), CDH23(NM_022124.6):c.3293A>G (p.N1098S) - CDH23_000034 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.3293A>G r.(?) p.(Asn1098Ser) - Parent #2 - VUS g.73472494A>G g.71712737A>G - - CDH23_000034 - PubMed: Bryant 2018 - rs41281310 Germline - - - - - DNA SEQ-NG - WES retinal disease JB40 PubMed: Bryant 2018 - - - United States - - - - - 1 LOVD
Legend   How to query  


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