Variant #0000002372 (NC_000004.11:g.84191124C>T, COQ2(NM_015697.7):c.801G>A)
      
      
        
          | Individual ID | 
          00002372 |  
        
          | Chromosome | 
          4 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Not classified |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.84191124C>T |  
        
          | Reference | 
          Ogaki K, Fujioka S, Heckman MG, Rayaprolu S, Soto-Ortolaza AI, Labbé C, Walton RL, Lorenzo-Betancor O, Wang X, Asmann Y, Rademakers R, Graff-Radford N, Uitti R, Cheshire WP, Wszolek ZK, Dickson DW, Ross OA1.(2014) |  
        
          | DB-ID | 
          COQ2_000008 |  
        
          | Frequency | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          0.00067 View details |  
        
          | Owner | 
          Y Yang |  
        
          | Database submission license | 
          Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
        
          | Created by | 
          Y Yang |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
  
      Screenings
       
      
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