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    | Variant #0000017007 (NC_000009.11:g.35657869C>T, NR_003051.3:n.147G>A (RMRP))
        
          | Chromosome | 9 |  
          | Allele | Parent #1 |  
          | 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.35657869C>T |  
          | DNA change (hg38) | g.35657872C>T |  
          | Published as | 146A; g.146G>A |  
          | ISCN | - |  
          | DB-ID | RMRP_000070 See all 2 reported entries |  
          | Variant remarks | 1 Chinese CHH family (hom), 1 French CHH family (com-het) and 2 CHH families (com-het)  with undetermined ethnicity |  
          | Reference | PubMed: Ridanpää et al. 2002, PubMed: Bonafe et al. 2005, PubMed: Kavadas et al. 2008 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | yes |  
          | Frequency | 0/280 CON |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | 5.0E-5 View details |  
          | Owner | Anne Polvi |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Anne Polvi |  
          | Date created | 2013-01-30 15:07:13 +01:00 (CET) |  
          | Date last edited | 2020-06-25 13:27:52 +02:00 (CEST) |   
 
 
 
       
 
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