Variant #0000244053 (NC_000017.10:g.44039791A>G, NM_001123066.3:c.88A>G (MAPT))
      
      
        
          | Chromosome | 
          17 |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Does not affect function |  
        
          | Affects function (by curator) | 
          Effect unknown |  
        
          | Classification method | 
          - |  
        
          | Clinical classification | 
          benign |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.44039791A>G |  
        
          | DNA change (hg38) | 
          g.45962425A>G |  
        
          | Published as | 
          - |  
        
          | ISCN | 
          - |  
        
          | DB-ID | 
          MAPT_000014 |  
        
          | Variant remarks | 
          Observed in 1 African  individual of the <a href=\""http://www.cephb.fr/en/hgdp/diversity.php/"""" target=blank> Human Genome Diversity Panel</a>. /r/Point mutation in coding region predicting an amino acid substitution"" |  
        
          | Reference | 
          - |  
        
          | ClinVar ID | 
          - |  
        
          | dbSNP ID | 
          - |  
        
          | Origin | 
          Unknown |  
        
          | Segregation | 
          - |  
        
          | Frequency | 
          - |  
        
          | Re-site | 
          - |  
        
          | VIP | 
          - |  
        
          | Methylation | 
          - |  
        
          | Average frequency (gnomAD v.2.1.1) | 
          3.0E-5 View details |  
        
          | Owner | 
          Marc Cruts |  
        
          | Database submission license | 
          Creative Commons Attribution 4.0 International   |  
        
          | Created by | 
          Julia Lopez |  
        
          | Date created | 
          2013-05-01 13:44:57 +02:00 (CEST) |  
        
          | Date last edited | 
          2020-07-13 16:29:42 +02:00 (CEST) |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
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