Variant #0000782078 (NC_000016.9:g.(?_2097990)_(2134717_2134951)del, NC_000016.9(NM_000548.3):c.(?_-106)_(4493+1_4494-1)del (TSC2))
      
      
        
          | Chromosome | 
          16 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Affects function |  
        
          | Affects function (by curator) | 
          Affects function |  
        
          | Classification method | 
          - |  
        
          | Clinical classification | 
          pathogenic (dominant) |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.(?_2097990)_(2134717_2134951)del |  
        
          | DNA change (hg38) | 
          g.(?_2047989)_(2084716_2084950)del |  
        
          | Published as | 
          - |  
        
          | ISCN | 
          - |  
        
          | DB-ID | 
          TSC2_003759 See all 2 reported entries |  
        
          | Variant remarks | 
          exons 1-34 deleted |  
        
          | Reference | 
          - |  
        
          | ClinVar ID | 
          - |  
        
          | dbSNP ID | 
          - |  
        
          | Origin | 
          SUMMARY record |  
        
          | Segregation | 
          - |  
        
          | Frequency | 
          - |  
        
          | Re-site | 
          - |  
        
          | VIP | 
          - |  
        
          | Methylation | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          Retrieve |  
        
          | Owner | 
          Rosemary Ekong |  
        
          | Database submission license | 
          Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
        
          | Created by | 
          Rosemary Ekong |  
        
          | Date created | 
          2021-05-04 16:22:13 +02:00 (CEST) |  
        
          | Date last edited | 
          N/A |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
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