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    | Variant #0000371900 (NC_000012.11:g.102164817dup, NM_024312.4:c.890dup (GNPTAB))
        
          | Chromosome | 12 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Affects function |  
          | Classification method | - |  
          | Clinical classification | pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.102164817dup |  
          | DNA change (hg38) | g.101771039dup |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | GNPTAB_000104 |  
          | Variant remarks | - |  
          | Reference | Journal: Wang et al. 2018 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | Germline/De novo (untested) |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Renata Voltolini Velho |  
          | Database submission license | No license selected |  
          | Created by | Renata Voltolini Velho |  
          | Date created | 2018-07-09 16:23:31 +02:00 (CEST) |  
          | Date last edited | 2018-08-01 09:14:55 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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