Variant #0000002646 (NC_000011.9:g.6638271G>A, TPP1(NM_000391.3):c.622C>T)
      
      
        
          | Individual ID | 
          00002646 |  
        
          | Chromosome | 
          11 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Not classified |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.6638271G>A |  
        
          | Reference | 
          Sleat et al. 1997 Science 277:1802-1805;Zhong et al. 1998 Clin Genet 54:234-238;Sleat et al. 1999 Am J Hum Genet 64:1511-1523;Hartikainen et al. 1999 Mol Genet Mab 67:162-168 |  
        
          | DB-ID | 
          TPP1_000020 |  
        
          | Frequency | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          0.00024 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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