Variant #0000604033 (NC_000011.9:g.5247878G>A, NM_000518.4:c.244C>T (HBB))
      
      
        
          | Chromosome | 
          11 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Effect unknown |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | Classification method | 
          - |  
        
          | Clinical classification | 
          VUS |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.5247878G>A |  
        
          | DNA change (hg38) | 
          g.5226648G>A |  
        
          | Published as | 
          CD 81 CTC>TTC [Leu>Phe] |  
        
          | ISCN | 
          - |  
        
          | DB-ID | 
          HBB_001760 See all 2 reported entries |  
        
          | Variant remarks | 
          β-chain variant |  
        
          | Reference | 
          IthaNet-2443 |  
        
          | ClinVar ID | 
          - |  
        
          | dbSNP ID | 
          - |  
        
          | Origin | 
          SUMMARY record |  
        
          | Segregation | 
          - |  
        
          | Frequency | 
          - |  
        
          | Re-site | 
          - |  
        
          | VIP | 
          - |  
        
          | Methylation | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          Retrieve |  
        
          | Owner | 
          IthaNet - Petros Kountouris |  
        
          | Database submission license | 
          Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
        
          | Created by | 
          Johan den Dunnen |  
        
          | Date created | 
          2019-11-08 15:46:08 +01:00 (CET) |  
        
          | Date last edited | 
          N/A |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
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