Variant #0001017007 (NC_000005.9:g.(112137081_112151191)_(112179824_?)del, NM_000038.5:c.(834+1_835-1)_(*2113_?)del (APC))
      
      
        
          | Chromosome | 
          5 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Affects function |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | Classification method | 
          ACMG |  
        
          | Clinical classification | 
          pathogenic |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.(112137081_112151191)_(112179824_?)del |  
        
          | DNA change (hg38) | 
          g.(112801384_112815494)_(112846239_?)del |  
        
          | Published as | 
          del ex9-16 |  
        
          | ISCN | 
          - |  
        
          | DB-ID | 
          APC_000536 See all 9 reported entries |  
        
          | Variant remarks | 
          ACMG PVS1, PS4, PM2_sup |  
        
          | Reference | 
          PubMed: Yin 2024, Journal: Yin 2024 |  
        
          | ClinVar ID | 
          - |  
        
          | dbSNP ID | 
          - |  
        
          | Origin | 
          SUMMARY record |  
        
          | Segregation | 
          - |  
        
          | Frequency | 
          - |  
        
          | Re-site | 
          - |  
        
          | VIP | 
          - |  
        
          | Methylation | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          Retrieve |  
        
          | Owner | 
          Stefan Aretz |  
        
          | Database submission license | 
          Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
        
          | Created by | 
          Johan den Dunnen |  
        
          | Date created | 
          2024-11-14 12:22:32 +01:00 (CET) |  
        
          | Date last edited | 
          N/A |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
     |