Table 3.

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

	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	+

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.