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    | Variant #0000409885 (NC_000013.10:g.32889449C>T, NM_000059.3:c.-395C>T (BRCA2))
        
          | Chromosome | 13 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Effect unknown |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | NA |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.32889449C>T |  
          | DNA change (hg38) | g.32315312C>T |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | BRCA2_006628 See all 2 reported entries |  
          | Variant remarks | expression cloning luciferase assay no effect |  
          | Reference | PubMed: Burke 2018, Journal:  Burke 2018 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | In vitro (cloned) |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Lez J Burke |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2018-10-27 18:08:29 +02:00 (CEST) |  
          | Date last edited | 2019-02-07 08:32:11 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
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