Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Insertion | NM_000059.4(BRCA2):c.4981_4982insG (p.Tyr1661Ter) | BRCA2 | Pathogenic | 13 | 32913473 | 32913474 | T | TG | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):5209&base_change=ins G,ClinGen:CA021098 |
Insertion | NM_000059.4(BRCA2):c.5074_5075insA (p.Trp1692Ter) | BRCA2 | Pathogenic | 13 | 32913566 | 32913567 | T | TA | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):5302&base_change=ins A,ClinGen:CA021214 |
Deletion | NM_000059.4(BRCA2):c.5222_5225del (p.Ser1741fs) | BRCA2 | Pathogenic | 13 | 32913711 | 32913714 | TTAAG | T | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):5450&base_change=del GTAA,ClinGen:CA021774 |
Insertion | NM_000059.4(BRCA2):c.5239_5240insT (p.Asn1747fs) | BRCA2 | Pathogenic | 13 | 32913731 | 32913732 | A | AT | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):5467&base_change=ins T,ClinGen:CA021833 |
Deletion | NM_000059.4(BRCA2):c.5270_5286del (p.Tyr1757fs) | BRCA2 | Pathogenic | 13 | 32913759 | 32913775 | GTATATAATGATTCAGGA | G | reviewed by expert panel | ClinGen:CA021904,Breast Cancer Information Core (BIC) (BRCA2):5498&base_change=del 17 |
Duplication | NM_000059.4(BRCA2):c.5492dup (p.Ser1832fs) | BRCA2 | Pathogenic | 13 | 32913983 | 32913984 | A | AT | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):5720&base_change=ins T,ClinGen:CA022431 |
single nucleotide variant | NM_000059.4(BRCA2):c.5682C>A (p.Tyr1894Ter) | BRCA2 | Pathogenic | 13 | 32914174 | 32914174 | C | A | reviewed by expert panel | ClinGen:CA022957 |
Deletion | NM_000059.4(BRCA2):c.5863del (p.Ser1955fs) | BRCA2 | Pathogenic | 13 | 32914354 | 32914354 | CT | C | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):6091&base_change=del T,ClinGen:CA023315 |
Duplication | NM_000059.3(BRCA2):c.6098dup (p.Arg2034fs) | BRCA2 | Pathogenic | 13 | 32914589 | 32914590 | A | AT | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):6325&base_change=ins T,ClinGen:CA023646 |
Insertion | NM_000059.4(BRCA2):c.6203_6204insA (p.Leu2069fs) | BRCA2 | Pathogenic | 13 | 32914695 | 32914696 | T | TA | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):6431&base_change=ins A,ClinGen:CA023741 |