Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NM_007294.4(BRCA1):c.241_251del (p.Gln81fs) | BRCA1 | Pathogenic | 17 | 41256935 | 41256945 | TTCAACAAGTTG | T | reviewed by expert panel | ClinGen:CA001606 |
Insertion | NM_007294.3(BRCA1):c.2504_2505ins17 (p.?) | BRCA1 | Pathogenic | 17 | 41245043 | 41245044 | na | na | criteria provided, single submitter | Breast Cancer Information Core (BIC) (BRCA1):2623&base_change=ins 17 |
single nucleotide variant | NM_007294.4(BRCA1):c.250G>T (p.Glu84Ter) | BRCA1 | Pathogenic | 17 | 41256936 | 41256936 | C | A | reviewed by expert panel | ClinGen:CA001662 |
Deletion | NM_007294.4(BRCA1):c.2654del (p.Phe885fs) | BRCA1 | Pathogenic | 17 | 41244894 | 41244894 | GA | G | reviewed by expert panel | ClinGen:CA001737 |
Duplication | NM_007294.4(BRCA1):c.2686dup (p.Ser896fs) | BRCA1 | Pathogenic | 17 | 41244861 | 41244862 | C | CT | reviewed by expert panel | ClinGen:CA001768 |
Deletion | NM_007294.4(BRCA1):c.2748del (p.Asn916fs) | BRCA1 | Pathogenic | 17 | 41244800 | 41244800 | TA | T | reviewed by expert panel | ClinGen:CA001810 |
Deletion | NM_007294.4(BRCA1):c.2774del (p.Ile925fs) | BRCA1 | Pathogenic | 17 | 41244774 | 41244774 | GA | G | reviewed by expert panel | ClinGen:CA001827 |
Duplication | NM_007294.4(BRCA1):c.2901_2902dup (p.Pro968fs) | BRCA1 | Pathogenic | 17 | 41244645 | 41244646 | G | GGA | reviewed by expert panel | ClinGen:CA001889 |
Deletion | NM_007294.4(BRCA1):c.2940del (p.Pro981fs) | BRCA1 | Pathogenic | 17 | 41244608 | 41244608 | GT | G | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):3059&base_change=del A,ClinGen:CA001921 |
Deletion | NM_007294.4(BRCA1):c.3204del (p.Gln1069fs) | BRCA1 | Pathogenic | 17 | 41244344 | 41244344 | GA | G | reviewed by expert panel | ClinGen:CA002081 |