Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NM_007294.4(BRCA1):c.2021del (p.Pro674fs) | BRCA1 | Pathogenic | 17 | 41245527 | 41245527 | AG | A | reviewed by expert panel | ClinGen:CA001348 |
Deletion | NM_007294.4(BRCA1):c.2028_2029del (p.Gly677fs) | BRCA1 | Pathogenic | 17 | 41245519 | 41245520 | CCA | C | reviewed by expert panel | ClinGen:CA001349 |
single nucleotide variant | NM_007294.4(BRCA1):c.2035A>T (p.Lys679Ter) | BRCA1 | Pathogenic | 17 | 41245513 | 41245513 | T | A | reviewed by expert panel | ClinGen:CA001353 |
Indel | NM_007294.4(BRCA1):c.2037delinsCC (p.Lys679fs) | BRCA1 | Pathogenic | 17 | 41245511 | 41245511 | C | GG | reviewed by expert panel | ClinGen:CA327800 |
Deletion | NM_007294.4(BRCA1):c.2048del (p.Lys683fs) | BRCA1 | Pathogenic | 17 | 41245500 | 41245500 | CT | C | reviewed by expert panel | ClinGen:CA001358 |
single nucleotide variant | NM_007294.4(BRCA1):c.2059C>T (p.Gln687Ter) | BRCA1 | Pathogenic | 17 | 41245489 | 41245489 | G | A | reviewed by expert panel | ClinGen:CA001363 |
Deletion | NM_007294.4(BRCA1):c.2063_2066del (p.Thr688fs) | BRCA1 | Pathogenic | 17 | 41245482 | 41245485 | ACTTG | A | reviewed by expert panel | ClinGen:CA001365 |
Deletion | NM_007294.4(BRCA1):c.2074del (p.His692fs) | BRCA1 | Pathogenic | 17 | 41245474 | 41245474 | TG | T | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):2193&base_change=del C,ClinGen:CA001372 |
Deletion | NM_007294.4(BRCA1):c.2075_2076del (p.His692fs) | BRCA1 | Pathogenic | 17 | 41245472 | 41245473 | CAT | C | reviewed by expert panel | ClinGen:CA001373 |
Deletion | NM_007294.4(BRCA1):c.2079_2080del (p.Asp693fs) | BRCA1 | Pathogenic | 17 | 41245468 | 41245469 | CTG | C | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):2198&base_change=del CA,ClinGen:CA001378 |