Variant #0000001116 (NC_000016.9:g.215400_234700del)
      
      
        
          | Individual ID | 
          00000003, 00000009, 00000039, 00000040, 00000042, 00000043, 00000046, 00000047, 00000048, 00000049, 00000051, 00000054, 00000055, 00000056, 00000057, 00000058, 00000059, 00000061, 00000063, 00000069, 00000070, 00000077, 00000079, 00000081, 00000086, 00000087, 00000088, 00000089, 00000090, 00000093, 00000094, 00000098, 00000099, 00000100, 00000101, 00000102, 00000105, 00000107, 00000108, 00000111, 00000112, 00000113, 00000119, 00000122, 00000124, 00000126, 00000127, 00000128, 00000129, 00000130, 00000132, 00000133, 00000134, 00000137, 00000139, 00000140, 00000141, 00000142, 00000143, 00000146, 00000147, 00000149, 00000151, 00000152, 00000154, 00000157, 00000158, 00000160, 00000161, 00000162, 00000163, 00000164, 00000165, 00000167, 00000168, 00000169, 00000170, 00000172, 00000173, 00000175, 00000176, 00000177, 00000192, 00000193, 00000194 |  
        
          | Chromosome | 
          16 |  
        
          | Allele | 
          Parent #1 |  
        
          | Affects function (as reported) | 
          Affects function |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | Type | 
          Deletion |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.215400_234700del |  
        
          | Reference | 
          Xu et al |  
        
          | DB-ID | 
          chr16_000013 |  
        
          | Frequency | 
          - |  
        
          | Variant remarks | 
          - -SEA |  
        
          | ClassClinical | 
          Pathogenic |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          Genomic location of variant could not be determined |  
        
          | Owner | 
          Qi Ming |  
        
          | Database submission license | 
          No license selected |  
        
          | Created by | 
          Qi Ming |   
      
  
      
       
      
  
      Variant on transcripts
      
      
      
      
  
      Screenings
       
      
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