| Variant #0000782068 (NC_000016.9:g.2097981G>T, NM_000548.3:c.-115G>T (TSC2))
        
          | Chromosome | 16 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Probably does not affect function |  
          | Affects function (by curator) | Probably does not affect function |  
          | Classification method | - |  
          | Clinical classification | likely benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.2097981G>T |  
          | DNA change (hg38) | g.2047980G>T |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | TSC2_002760 See all 2 reported entries |  
          | Variant remarks | variant is 9 bases 5' of the untranslated exon 1 and is between 2 cETS binding sites in the core promoter region (Kobayashi et al, 1997. DOI: 10.1007/s003359900502) |  
          | Reference | - |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | MmeI+ |  
          | 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 | 2021-05-04 16:22:13 +02:00 (CEST) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
 |