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Table 5 Haplotype analyses in the BRCA1 c.676delT carrier families

From: Tracking of the origin of recurrent mutations of the BRCA1 and BRCA2 genes in the North-East of Italy and improved mutation analysis strategy

  D17S588 D17S806 D17S902 D17S855 (BRCA1) a D17S1328 D17S800 D17S250
BR128 154-156 168-170 149-149 149–153 247–247 170–174 153–159
BR328 154–154 170–172 149–153 147–149 247–247 166–174 149–159
BR384 148–154 170–178 145–149 149–155 247–249 174–174 149–159
BR392 154–159 168–170 149–153 145–149 247–247 174–174 145–155
BR573 154–156 162–176 149–153 147–149 247–251 170–174 149–153
BR613 138–154 170–172 149–153 143–149 247–247 170–174 149–149
BR704 140–154 170–176 145–149 147–149 247–247 170–176 145–155
BR977 154–156 170–174 149–157 149–153 247–247 170–174 151–153
BR1091 148–154 170–170 149–157 149–151 247–247 170–174 151–161
  1. Alleles segregating with the mutation inside each family are represented in bold type. The 149–149–247 shared haplotype is underlined
  2. a D17S855 is located into the BRCA1 locus