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    | Variant #0000674788 (NC_000016.9:g.2106894_2161281del, NM_000548.3:c.774+124_*102{0} (TSC2))
        
          | Chromosome | 16 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Affects function |  
          | Classification method | - |  
          | Clinical classification | pathogenic (dominant) |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.2106894_2161281del |  
          | DNA change (hg38) | g.2056893_2088712{0} |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | TSC2_001558 See all 2 reported entries |  
          | Variant remarks | deletion includes TSC2 exons 9-42 and PKD1 exons 15-46 (PKD1 variant = c.3887_*1017{0}); 54,388bp genomic deletion with breakpoints determined; starts in TSC2 intron 8 (NM_000548.3:c.774+125) and ends in PKD1 exon 15 (NM_000296.3:c.3887) |  
          | Reference | - |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Rosemary Ekong |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Rosemary Ekong |  
          | Date created | 2020-07-20 14:30:39 +02:00 (CEST) |  
          | Date last edited | 2021-08-18 14:45:40 +02:00 (CEST) |   
 
 
 
       
 
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