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Table 3 Genotype analysis of flanking microsatellites associated with the 9106C>T BRCA2 mutation.

From: Phenotypic features and genetic characterization of male breast cancer families: identification of two recurrent BRCA2 mutations in north-east of Italy

  Markers carrier (+)/non carrier (-)
  Probands D13S290 D13S260 D13S1698 D13S171 D13S1695  
Family 25        
  BR22 5-5 6-5 2-2 6-6 6-5 +
  BR23 5-5 5-3 2-5 6-1 5-8 -
  BR99 5-3 2-2 4–6 2-2 5–7 -
  BR100 5-4 6-2 2-4 6-2 6-5 +
  BR101 5-5 6-1 2-5 6-2 6-2 +
  BR102 5-4 6-2 2-4 6-2 6-5 +
  BR103 5-5 5-3 2–5 6-1 5–8 -
Isolated cases        
  BR175 5,4 1,4 1,1 6,2 6,5 +
  BR342 5,3 1,3 1,3 6,2 6,6 +
  TBL38 5,5 1,5 1,5 6,2 6,6 +
  1. Numbers in boldface type indicate the 9106C>T mutation alleles. Haplotype segregating with the 9106C>T mutation alleles of phased alleles are separated by a dash. Genotypes of unphased alleles are separated by a comma.