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    | Variant #0000191059 (NC_000017.10:g.41277103A>C, NC_000017.10(NM_007294.3):c.-20+185T>G (BRCA1))
        
          | Chromosome | 17 |  
          | Allele | Parent #1 |  
          | Affects function (as reported) | Does not affect function |  
          | Affects function (by curator) | Does not affect function |  
          | Classification method | - |  
          | Clinical classification | benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.41277103A>C |  
          | DNA change (hg38) | g.43125086A>C |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | BRCA1_004584 |  
          | Variant remarks | Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.02033 (African), derived from 1000 genomes (2012-04-30). |  
          | Reference | ENIGMA classification criteria |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | ENIGMA consortium |  
          | Database submission license | Creative Commons Attribution 4.0 International   |  
          | Created by | ENIGMA consortium |  
          | Date created | 2015-12-01 12:00:00 +01:00 (CET) |  
          | Date last edited | 2018-08-22 13:58:24 +02:00 (CEST) |   
 
 
 
       
 
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