Indel | NM_007294.4(BRCA1):c.2392_2393delinsA (p.Pro798fs) | BRCA1 | Pathogenic | 17 | 41245155 | 41245156 | GG | T | criteria provided, single submitter | ClinGen:CA658656696 |
Deletion | NM_007294.4(BRCA1):c.3083del (p.Arg1028fs) | BRCA1 | Pathogenic | 17 | 41244465 | 41244465 | AC | A | criteria provided, single submitter | ClinGen:CA626221301 |
single nucleotide variant | NM_007294.4(BRCA1):c.1154G>A (p.Trp385Ter) | BRCA1 | Pathogenic | 17 | 41246394 | 41246394 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10599747 |
Deletion | NM_007294.4(BRCA1):c.3870_3877del (p.Lys1290fs) | BRCA1 | Pathogenic | 17 | 41243671 | 41243678 | GCAGAACAT | G | criteria provided, single submitter | ClinGen:CA658656674 |
Deletion | NM_007294.4(BRCA1):c.998_1010del (p.Thr333fs) | BRCA1 | Pathogenic | 17 | 41246538 | 41246550 | TTCTGTGCTGGGAG | T | criteria provided, single submitter | ClinGen:CA658656801 |
Deletion | NM_007294.4(BRCA1):c.799del (p.Ser267fs) | BRCA1 | Pathogenic | 17 | 41246749 | 41246749 | GA | G | criteria provided, single submitter | ClinGen:CA658656633 |
Indel | NM_007294.4(BRCA1):c.1929_1930delinsA (p.Ser643fs) | BRCA1 | Pathogenic | 17 | 41245618 | 41245619 | AA | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656743 |
Deletion | NM_007294.4(BRCA1):c.1676del (p.Gly559fs) | BRCA1 | Pathogenic | 17 | 41245872 | 41245872 | AC | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656759 |
Indel | NM_007294.4(BRCA1):c.288_292delinsAACCTGT (p.Asp96fs) | BRCA1 | Pathogenic | 17 | 41256894 | 41256898 | CTGTG | ACAGGTT | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656667 |
Deletion | NM_007294.4(BRCA1):c.83del (p.Leu28fs) | BRCA1 | Pathogenic | 17 | 41267794 | 41267794 | CA | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656690 |