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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.