Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NM_007294.4(BRCA1):c.399_400del (p.Ala134fs) | BRCA1 | Pathogenic | 17 | 41256180 | 41256181 | GCA | G | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):517&base_change=del GT,ClinGen:CA002554 |
single nucleotide variant | NM_007294.4(BRCA1):c.3G>T (p.Met1Ile) | BRCA1 | Pathogenic | 17 | 41276111 | 41276111 | C | A | reviewed by expert panel | ClinGen:CA002562 |
Deletion | NM_007294.4(BRCA1):c.4001del (p.Gly1334fs) | BRCA1 | Pathogenic | 17 | 41243547 | 41243547 | AC | A | reviewed by expert panel | ClinGen:CA002564 |
Deletion | NM_007294.4(BRCA1):c.4002_4005del (p.Leu1335fs) | BRCA1 | Pathogenic | 17 | 41243543 | 41243546 | TCAGA | T | reviewed by expert panel | ClinGen:CA002565 |
Deletion | NM_007294.4(BRCA1):c.4043del (p.Gly1348fs) | BRCA1 | Pathogenic | 17 | 41243505 | 41243505 | TC | T | reviewed by expert panel | ClinGen:CA002582 |
Duplication | NM_007294.4(BRCA1):c.4049dup (p.Glu1352fs) | BRCA1 | Pathogenic | 17 | 41243498 | 41243499 | G | GC | reviewed by expert panel | ClinGen:CA327907 |
single nucleotide variant | NM_007294.4(BRCA1):c.4052T>A (p.Leu1351Ter) | BRCA1 | Pathogenic | 17 | 41243496 | 41243496 | A | T | reviewed by expert panel | ClinGen:CA002587 |
Duplication | NM_007294.4(BRCA1):c.4052dup (p.Leu1351fs) | BRCA1 | Pathogenic | 17 | 41243495 | 41243496 | C | CA | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):4171&base_change=ins T,ClinGen:CA002586 |
single nucleotide variant | NM_007294.4(BRCA1):c.4057G>T (p.Glu1353Ter) | BRCA1 | Pathogenic | 17 | 41243491 | 41243491 | C | A | reviewed by expert panel | ClinGen:CA002592 |
Deletion | NM_007294.4(BRCA1):c.4057_4061del (p.Glu1352_Glu1353insTer) | BRCA1 | Pathogenic | 17 | 41243487 | 41243491 | ATTTTC | A | reviewed by expert panel | ClinGen:CA002591 |