Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NM_000059.4(BRCA2):c.2961del (p.Asn987fs) | BRCA2 | Pathogenic | 13 | 32911453 | 32911453 | AT | A | reviewed by expert panel | ClinGen:CA10586508 |
single nucleotide variant | NM_000059.4(BRCA2):c.3016G>T (p.Gly1006Ter) | BRCA2 | Pathogenic | 13 | 32911508 | 32911508 | G | T | reviewed by expert panel | ClinGen:CA10586509 |
single nucleotide variant | NM_000059.4(BRCA2):c.3046G>T (p.Glu1016Ter) | BRCA2 | Pathogenic | 13 | 32911538 | 32911538 | G | T | reviewed by expert panel | ClinGen:CA6940656 |
Deletion | NM_000059.4(BRCA2):c.3175del (p.Lys1058_Leu1059insTer) | BRCA2 | Pathogenic | 13 | 32911667 | 32911667 | AC | A | reviewed by expert panel | ClinGen:CA10586510 |
Deletion | NM_000059.4(BRCA2):c.3293del (p.Asn1098fs) | BRCA2 | Pathogenic | 13 | 32911784 | 32911784 | TA | T | reviewed by expert panel | ClinGen:CA017716 |
Deletion | NM_000059.4(BRCA2):c.3295del (p.Ser1099fs) | BRCA2 | Pathogenic | 13 | 32911786 | 32911786 | AT | A | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):3522&base_change=del T,ClinGen:CA017723 |
Duplication | NM_000059.4(BRCA2):c.3455dup (p.Leu1152fs) | BRCA2 | Pathogenic | 13 | 32911945 | 32911946 | C | CT | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):3681&base_change=ins T,ClinGen:CA018080 |
Duplication | NM_000059.4(BRCA2):c.3593dup (p.Asn1198fs) | BRCA2 | Pathogenic | 13 | 32912080 | 32912081 | G | GA | reviewed by expert panel | ClinGen:CA280072 |
Deletion | NM_000059.4(BRCA2):c.3599del (p.Cys1200fs) | BRCA2 | Pathogenic | 13 | 32912091 | 32912091 | TG | T | reviewed by expert panel | ClinGen:CA10586511 |
Deletion | NM_000059.4(BRCA2):c.3639_3652del (p.Val1214fs) | BRCA2 | Pathogenic | 13 | 32912131 | 32912144 | AAGTGGGGTTTAGGG | A | reviewed by expert panel | ClinGen:CA10586512 |