Variant #0000016730 (NC_000002.11:g.136590751_136590752del, NM_002299.2:c.653_654del (LCT))
      
      
        
          | Chromosome | 
          2 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Affects function |  
        
          | Affects function (by curator) | 
          Affects function |  
        
          | Classification method | 
          - |  
        
          | Clinical classification | 
          pathogenic |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.136590751_136590752del |  
        
          | DNA change (hg38) | 
          g.135833181_135833182del |  
        
          | Published as | 
          c.653_654delCT:S218fsX224 |  
        
          | ISCN | 
          - |  
        
          | DB-ID | 
          LCT_000001 |  
        
          | Variant remarks | 
          1 Finnish family (com-het) with lactase deficiency, congenital |  
        
          | Reference | 
          PubMed: Kuokkanen et al. 2006 |  
        
          | ClinVar ID | 
          - |  
        
          | dbSNP ID | 
          - |  
        
          | Origin | 
          SUMMARY record |  
        
          | Segregation | 
          yes |  
        
          | Frequency | 
          0/556 FIN CON |  
        
          | Re-site | 
          - |  
        
          | VIP | 
          - |  
        
          | Methylation | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          Retrieve |  
        
          | Owner | 
          Anne Polvi |  
        
          | Database submission license | 
          Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
        
          | Created by | 
          Anne Polvi |  
        
          | Date created | 
          2012-12-10 17:13:21 +01:00 (CET) |  
        
          | Date last edited | 
          2020-06-09 13:20:56 +02:00 (CEST) |   
        
      
      
      
  
      
       
      
  
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