Variant #0000002666 (NC_000011.9:g.6637564T>G, TPP1(NM_000391.3):c.1057A>C)
      
      
        
          | Individual ID | 
          00002666 |  
        
          | Chromosome | 
          11 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Not classified |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.6637564T>G |  
        
          | Reference | 
          Steinfeld et al. 2002 Am J Med Geent 112:347-354 |  
        
          | DB-ID | 
          TPP1_000040 |  
        
          | Frequency | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          Retrieve |  
        
          | 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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