| Variant #0000540776 (NC_000010.10:g.73571123G>C, NM_022124.5:c.9129G>C (CDH23))
        
          | Chromosome | 10 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Probably does not affect function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | likely benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.73571123G>C |  
          | DNA change (hg38) | g.71811366G>C |  
          | Published as | CDH23(NM_022124.5):c.9129G>C (p.R3043=) |  
          | ISCN | - |  
          | DB-ID | CDH23_000762 |  
          | Variant remarks | VKGL data sharing initiative Nederland |  
          | Reference | - |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | CLASSIFICATION record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | VKGL-NL_Rotterdam |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Rotterdam |  
          | Date created | 2019-07-18 18:22:55 +02:00 (CEST) |  
          | Date last edited | 2020-06-27 16:46:52 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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