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.

3 entries on 1 page. Showing entries 1 - 3.
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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     
-/. - c.9014C>G r.(?) p.(Ala3005Gly) - Unknown - benign g.73570263C>G g.71810506C>G CDH23(NM_001171933.1):c.2294C>G (p.(Ala765Gly)), CDH23(NM_022124.5):c.9014C>G (p.A3005G), CDH23(NM_022124.6):c.9014C>G (p.A3005G) - CDH23_000567 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.9014C>G r.(?) p.(Ala3005Gly) - Unknown - VUS g.73570263C>G g.71810506C>G CDH23(NM_001171933.1):c.2294C>G (p.(Ala765Gly)), CDH23(NM_022124.5):c.9014C>G (p.A3005G), CDH23(NM_022124.6):c.9014C>G (p.A3005G) - CDH23_000567 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.9014C>G r.(?) p.(Ala3005Gly) - Unknown - likely benign g.73570263C>G - CDH23(NM_001171933.1):c.2294C>G (p.(Ala765Gly)), CDH23(NM_022124.5):c.9014C>G (p.A3005G), CDH23(NM_022124.6):c.9014C>G (p.A3005G) - CDH23_000567 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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