Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Duplication | NM_000059.4(BRCA2):c.2526dup (p.Ala843fs) | BRCA2 | Pathogenic | 13 | 32911017 | 32911018 | T | TA | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):2754&base_change=ins A,ClinGen:CA015550 |
Deletion | NM_000059.4(BRCA2):c.2595del (p.Glu866fs) | BRCA2 | Pathogenic | 13 | 32911086 | 32911086 | GA | G | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):2823&base_change=del A,ClinGen:CA015752 |
Deletion | NM_000059.4(BRCA2):c.71_96del (p.Asp23_Leu24insTer) | BRCA2 | Pathogenic | 13 | 32893215 | 32893240 | ATTTAGGACCAATAAGTCTTAATTGGT | A | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):299&base_change=del 26,ClinGen:CA024953 |
Insertion | NM_000059.4(BRCA2):c.2833_2834insTT (p.Lys945fs) | BRCA2 | Pathogenic | 13 | 32911325 | 32911326 | A | ATT | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):3061&base_change=ins TT,ClinGen:CA016538 |
Duplication | NM_000059.4(BRCA2):c.2842dup (p.Val948fs) | BRCA2 | Pathogenic | 13 | 32911332 | 32911333 | T | TG | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):3070&base_change=ins G,ClinGen:CA016597 |
Deletion | NM_000059.4(BRCA2):c.2930_2940del (p.Ser976_Leu977insTer) | BRCA2 | Pathogenic | 13 | 32911421 | 32911431 | CTTGAATATAGA | C | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):3158&base_change=del 11,ClinGen:CA016825 |
single nucleotide variant | NM_000059.4(BRCA2):c.2978G>A (p.Trp993Ter) | BRCA2 | Pathogenic | 13 | 32911470 | 32911470 | G | A | reviewed by expert panel | ClinGen:CA016937 |
Duplication | NM_000059.4(BRCA2):c.106dup (p.Ser36fs) | BRCA2 | Pathogenic | 13 | 32893249 | 32893250 | C | CT | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):334&base_change=ins T,ClinGen:CA010719 |
single nucleotide variant | NM_000059.4(BRCA2):c.3362C>A (p.Ser1121Ter) | BRCA2 | Pathogenic | 13 | 32911854 | 32911854 | C | A | reviewed by expert panel | ClinGen:CA017863 |
Insertion | NM_000059.3(BRCA2):c.3407_3408ins100 (p.?) | BRCA2 | Pathogenic | 13 | 32911899 | 32911900 | na | na | criteria provided, single submitter | Breast Cancer Information Core (BIC) (BRCA2):3635&base_change=ins 100 |