Variant #0000613864 (NC_000012.11:g.111885856G>C, NM_002973.3:c.*4760C>G (ATXN2))
      
      
        
          | Chromosome | 
          12 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Probably does not affect function |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | Classification method | 
          - |  
        
          | Clinical classification | 
          likely benign |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.111885856G>C |  
        
          | DNA change (hg38) | 
          g.111448052G>C |  
        
          | Published as | 
          SH2B3(NM_005475.2):c.1478G>C (p.G493A) |  
        
          | ISCN | 
          - |  
        
          | DB-ID | 
          ATXN2_000051 |  
        
          | Variant remarks | 
          VKGL data sharing initiative Nederland |  
        
          | Reference | 
          - |  
        
          | ClinVar ID | 
          - |  
        
          | dbSNP ID | 
          - |  
        
          | Origin | 
          CLASSIFICATION record |  
        
          | Segregation | 
          - |  
        
          | Frequency | 
          - |  
        
          | Re-site | 
          - |  
        
          | VIP | 
          - |  
        
          | Methylation | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          Retrieve |  
        
          | Owner | 
          VKGL-NL_Rotterdam |  
        
          | Database submission license | 
          Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
        
          | Created by | 
          VKGL-NL_Rotterdam |  
        
          | Date created | 
          2019-12-04 15:24:38 +01:00 (CET) |  
        
          | Date last edited | 
          2020-03-23 16:13:27 +01:00 (CET) |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
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