Variant #0000401476 (NC_000016.9:g.2546390_2546401del, NM_001199107.1:c.241_252del (TBC1D24))
      
      
        
          | Chromosome | 
          16 |  
        
          | Allele | 
          Maternal (confirmed) |  
        
          | Affects function (as reported) | 
          Probably affects function |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | Classification method | 
          - |  
        
          | Clinical classification | 
          likely pathogenic |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.2546390_2546401del |  
        
          | DNA change (hg38) | 
          g.2496389_2496400del |  
        
          | Published as | 
          - |  
        
          | ISCN | 
          - |  
        
          | DB-ID | 
          TBC1D24_000075 See all 10 reported entries |  
        
          | Variant remarks | 
          - |  
        
          | Reference | 
          - |  
        
          | ClinVar ID | 
          - |  
        
          | dbSNP ID | 
          - |  
        
          | Origin | 
          Somatic |  
        
          | Segregation | 
          yes |  
        
          | Frequency | 
          - |  
        
          | Re-site | 
          - |  
        
          | VIP | 
          - |  
        
          | Methylation | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          Retrieve |  
        
          | Owner | 
          Jing Zhang |  
        
          | Database submission license | 
          No license selected |  
        
          | Created by | 
          Jing Zhang |  
        
          | Date created | 
          2018-08-20 04:53:02 +02:00 (CEST) |  
        
          | Date last edited | 
          2018-08-20 16:45:48 +02:00 (CEST) |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
  
      Screenings
      
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