Table S1. Ancestry information of all Mexican Genome Diversity Project samples included in the sequencing analysis. (XLSX 34 kb
Tables showing patient details according to the genetic background. (DOCX 184 kb
Deleterious BRCA1/2 germline mutations in Pakistani patients with TNBC. (DOCX 24Â kb
Table S6. Results of the top candidate SNPs analyzed using RegulomeDB (XLSX 12 kb
Table S2. All variants detected in BRCA1 in the 3842 SIGMA samples, together with their annotation. ...
Table S3. All variants detected in BRCA2 in the 3842 SIGMA samples, together with their annotation. ...
Table S3. Breast cancer tumour phenotypes according to BRCA1 and BRCA2 mutated cases. (DOC 14 kb
Breast cancer (BC) patients considered for the study, their age at diagnosis and the number of affec...
Tables S2-S5. Supplementary tables including linkage disequilibrium between top SNPs and previously ...
BC patients vs. controls variant types enrichment in exome- and CAGP-wide. (XLSX 10 kb
List with PDAVs detected in 54âBC patients located in genes linked to (hereditary) cancer and/or h...
Types and number of variants detected (exome- and CAGP-wide) before and after variant filtration in ...
Cancer, family-history, and BRCA1/2 status for all patients. This file indicates cancer, family hist...
Table S5. Manufacturer and clone information for antibodies used for IHC analyses. (DOCX 18 kb
Table S5. BRCA2 pathological germline mutations according to selection criteria and clinical charact...
Supplementary Methods. Table S1. Clinical and pathological characteristics, BRCA sequencing and MLPA...
Tables showing patient details according to the genetic background. (DOCX 184 kb
Deleterious BRCA1/2 germline mutations in Pakistani patients with TNBC. (DOCX 24Â kb
Table S6. Results of the top candidate SNPs analyzed using RegulomeDB (XLSX 12 kb
Table S2. All variants detected in BRCA1 in the 3842 SIGMA samples, together with their annotation. ...
Table S3. All variants detected in BRCA2 in the 3842 SIGMA samples, together with their annotation. ...
Table S3. Breast cancer tumour phenotypes according to BRCA1 and BRCA2 mutated cases. (DOC 14 kb
Breast cancer (BC) patients considered for the study, their age at diagnosis and the number of affec...
Tables S2-S5. Supplementary tables including linkage disequilibrium between top SNPs and previously ...
BC patients vs. controls variant types enrichment in exome- and CAGP-wide. (XLSX 10 kb
List with PDAVs detected in 54âBC patients located in genes linked to (hereditary) cancer and/or h...
Types and number of variants detected (exome- and CAGP-wide) before and after variant filtration in ...
Cancer, family-history, and BRCA1/2 status for all patients. This file indicates cancer, family hist...
Table S5. Manufacturer and clone information for antibodies used for IHC analyses. (DOCX 18 kb
Table S5. BRCA2 pathological germline mutations according to selection criteria and clinical charact...
Supplementary Methods. Table S1. Clinical and pathological characteristics, BRCA sequencing and MLPA...
Tables showing patient details according to the genetic background. (DOCX 184 kb
Deleterious BRCA1/2 germline mutations in Pakistani patients with TNBC. (DOCX 24Â kb
Table S6. Results of the top candidate SNPs analyzed using RegulomeDB (XLSX 12 kb