Variant #0000016673 (NC_000011.9:g.2846C>T, TMEM151A(NM_153266.4):c.469C>T)
      
      
        
          | Individual ID | 
          00002117 |  
        
          | Chromosome | 
          11 |  
        
          | Allele | 
          Maternal (confirmed) |  
        
          | Affects function (as reported) | 
          Effect unknown |  
        
          | Affects function (by curator) | 
          Probably affects function |  
        
          | Type | 
          Substitution |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.2846C>T |  
        
          | Reference | 
          GenBank |  
        
          | DB-ID | 
          TMEM151A_000469 |  
        
          | Frequency | 
          - |  
        
          | Variant remarks | 
          identified in a PKD family(Mov Disord. 2022;37(3):608-613) |  
        
          | ClassClinical | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          Retrieve |  
        
          | Owner | 
          Yulan Chen |  
        
          | Database submission license | 
          Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International   |  
        
          | Created by | 
          Yulan Chen |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
  
      Screenings
       
      
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