|   
  
    | Variant #0000016210 (NC_000009.11:g.35658020_35658036dup, NR_003051.3:n.-19_-3dupTCTGTGAAGCTGAGGAC (RMRP))
        
          | Chromosome | 9 |  
          | Allele | Paternal (confirmed) |  
          | Affects function (as reported) | Probably affects function |  
          | Affects function (by curator) | Probably affects function |  
          | Classification method | - |  
          | Clinical classification | likely pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.35658020_35658036dup |  
          | DNA change (hg38) | g.35658023_35658039dup |  
          | Published as | dupTCTGTGAAGCTGAGGAC at g.-3; -20_-4dupTCTGTGAAGCTGAGGAC |  
          | ISCN | - |  
          | DB-ID | RMRP_000026 |  
          | Variant remarks | 1 English and 1 Swiss CHH family (both com-het) |  
          | Reference | PubMed: Ridanpää et al. 2001, PubMed: Ridanpää et al. 2002, PubMed: Bonafe et al. 2005 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | yes |  
          | Frequency | 0/280 CON |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Anne Polvi |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Anne Polvi |  
          | Date created | 2012-11-08 13:14:45 +01:00 (CET) |  
          | Date last edited | 2020-06-25 13:33:07 +02:00 (CEST) |   
 
 
 
       
 
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