Variant #0000004398 (NC_000021.8:g.45194178G>A, CSTB(NM_000100.3):c.202C>T)
      
      
        
          | Individual ID | 
          00004398 |  
        
          | Chromosome | 
          21 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Not classified |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.45194178G>A |  
        
          | Reference | 
          Pennacchio LA1, Lehesjoki AE, Stone NE, Willour VL, Virtaneva K, Miao J, D'Amato E, Ramirez L, Faham M, Koskiniemi M, Warrington JA, Norio R, de la (1996) |  
        
          | DB-ID | 
          CSTB_000002 See all 3 reported entries |  
        
          | Frequency | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          4.0E-5 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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