Indel | NM_007294.4(BRCA1):c.5209_5248delinsTC (p.Arg1737fs) | BRCA1 | Pathogenic | 17 | 41209098 | 41209137 | TTGGACCTTGGTGGTTTCTTCCATTGACCACATCTCCTCT | GA | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):5328&base_change=del 40 ins TC,ClinGen:CA003359 |
Deletion | NM_007294.4(BRCA1):c.520del (p.Gln174fs) | BRCA1 | Pathogenic | 17 | 41251819 | 41251819 | TG | T | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):639&base_change=del C,ClinGen:CA003362 |
single nucleotide variant | NM_007294.4(BRCA1):c.5212G>A (p.Gly1738Arg) | BRCA1 | Pathogenic | 17 | 41209134 | 41209134 | C | T | reviewed by expert panel | BRCA1-HCI:BRCA1_00043,ClinGen:CA003363,UniProtKB:P38398#VAR_063907 |
single nucleotide variant | NM_007294.4(BRCA1):c.5213G>A (p.Gly1738Glu) | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41209133 | 41209133 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA003365 |
single nucleotide variant | NM_007294.4(BRCA1):c.5215G>T (p.Asp1739Tyr) | BRCA1 | Likely pathogenic | 17 | 41209131 | 41209131 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA003366 |
single nucleotide variant | NM_007294.4(BRCA1):c.5216A>G (p.Asp1739Gly) | BRCA1 | Likely pathogenic | 17 | 41209130 | 41209130 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA003367,UniProtKB:P38398#VAR_070507 |
single nucleotide variant | NM_007294.4(BRCA1):c.5216A>T (p.Asp1739Val) | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41209130 | 41209130 | T | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA003368,UniProtKB:P38398#VAR_070508 |
single nucleotide variant | NM_007294.4(BRCA1):c.5217T>G (p.Asp1739Glu) | BRCA1 | Likely pathogenic | 17 | 41209129 | 41209129 | A | C | criteria provided, single submitter | ClinGen:CA003370 |
Deletion | NM_007294.4(BRCA1):c.5229_5230del (p.Arg1744fs) | BRCA1 | Pathogenic | 17 | 41209116 | 41209117 | CTT | C | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):5348&base_change=del AA,ClinGen:CA003372 |
Deletion | NM_007294.4(BRCA1):c.5230del (p.Arg1744fs) | BRCA1 | Pathogenic | 17 | 41209116 | 41209116 | CT | C | reviewed by expert panel | ClinGen:CA003374 |