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    | Variant #0000626532 (NC_000002.11:g.96781203_96781214delinsCTGCCAAAC, NM_000682.5:c.675_686delinsGTTTGGCAG (ADRA2B))
        
          | Chromosome | 2 |  
          | Allele | Parent #1 |  
          | Affects function (as reported) | Effect unknown |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | VUS |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.96781203_96781214delinsCTGCCAAAC |  
          | DNA change (hg38) | g.96115464_96115475delinsCTGCCAAAC |  
          | Published as | 675_686delTGGTGGGGCTTTinsGTTTGGCAG |  
          | ISCN | - |  
          | DB-ID | ADRA2B_000005 See all 3 reported entries |  
          | Variant remarks | variant initially linked to ADCME phenotype |  
          | Reference | PubMed: Corbett 2019 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Johan den Dunnen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2019-12-19 14:02:00 +01:00 (CET) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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