Variant #0000016223 (NC_000009.11:g.35658015_35658018dup, NR_003051.3:n.-3_1dupCGTG (RMRP))
      
      
        
          | Chromosome | 
          9 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Probably affects function |  
        
          | Affects function (by curator) | 
          Probably affects function |  
        
          | Classification method | 
          - |  
        
          | Clinical classification | 
          likely pathogenic |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.35658015_35658018dup |  
        
          | DNA change (hg38) | 
          g.35658018_35658021dup |  
        
          | Published as | 
          -4_-1dup |  
        
          | ISCN | 
          - |  
        
          | DB-ID | 
          RMRP_000038 |  
        
          | Variant remarks | 
          1 CHH family (com-het) with undetermined ethnicity |  
        
          | Reference | 
          PubMed: Kavadas et al. 2008 |  
        
          | ClinVar ID | 
          - |  
        
          | dbSNP ID | 
          - |  
        
          | Origin | 
          SUMMARY record |  
        
          | Segregation | 
          yes |  
        
          | Frequency | 
          - |  
        
          | Re-site | 
          - |  
        
          | VIP | 
          - |  
        
          | Methylation | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          Retrieve |  
        
          | Owner | 
          Anne Polvi |  
        
          | Database submission license | 
          Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
        
          | Created by | 
          Anne Polvi |  
        
          | Date created | 
          2012-11-12 13:58:01 +01:00 (CET) |  
        
          | Date last edited | 
          2017-05-05 18:33:04 +02:00 (CEST) |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
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