Variant #0000545198 (NC_000011.9:g.6645459G>A, NM_000391.3:c.-4828C>T (TPP1))
      
      
        
          | Chromosome | 
          11 |  
        
          | 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.6645459G>A |  
        
          | DNA change (hg38) | 
          g.6624228G>A |  
        
          | Published as | 
          DCHS1(NM_003737.2):c.7448C>T (p.(Thr2483Ile)), DCHS1(NM_003737.2):c.7451C>T (p.S2484L) |  
        
          | ISCN | 
          - |  
        
          | DB-ID | 
          DCHS1_000135 See all 2 reported entries |  
        
          | 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) | 
          0.00089 View details |  
        
          | Owner | 
          VKGL-NL_Leiden |  
        
          | Database submission license | 
          Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
        
          | Created by | 
          VKGL-NL_Leiden |  
        
          | Date created | 
          2019-07-18 18:22:55 +02:00 (CEST) |  
        
          | Date last edited | 
          2019-12-04 15:24:38 +01:00 (CET) |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
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