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    | Variant #0000054171 (NC_000017.10:g.41276061A>G, NM_007294.3:c.53T>C (BRCA1))
        
          | Chromosome | 17 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | NA |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.41276061A>G |  
          | DNA change (hg38) | g.43124044A>G |  
          | Published as | M18T |  
          | ISCN | - |  
          | DB-ID | BRCA1_000011 See all 26 reported entries |  
          | Variant remarks | evolutionary conservation analysis; predicted deleterious |  
          | Reference | PubMed: Pettigrew 2005 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | In vitro (cloned) |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Peter Devilee |  
          | Database submission license | Creative Commons Attribution 4.0 International   |  
          | Created by | Maaike Vreeswijk |  
          | Date created | 2009-10-03 16:24:58 +02:00 (CEST) |  
          | Date last edited | 2020-07-13 15:54:19 +02:00 (CEST) |   
 
 
 
       
 
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