Variant #0000002456 (NC_000007.13:g.143042856G>T, CLCN1(NM_000083.2):c.2172+1G>T)
      
      
        
          | Individual ID | 
          00002456 |  
        
          | Chromosome | 
          7 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Not classified |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.143042856G>T |  
        
          | Reference | 
          Chen L1, Schaerer M, Lu ZH, Lang D, Joncourt F, Weis J, Fritschi J, Kappeler L, Gallati S, Sigel E, Burgunder JM.(2004) |  
        
          | DB-ID | 
          CLCN1_000090 |  
        
          | Frequency | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          1.0E-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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