Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NM_000059.4(BRCA2):c.3720_3721del (p.Leu1240_Phe1241insTer) | BRCA2 | Pathogenic | 13 | 32912211 | 32912212 | CTG | C | reviewed by expert panel | ClinGen:CA645509344 |
Deletion | NM_000059.4(BRCA2):c.4710del (p.Glu1571fs) | BRCA2 | Pathogenic | 13 | 32913202 | 32913202 | GA | G | reviewed by expert panel | ClinGen:CA645509348 |
Duplication | NM_000059.4(BRCA2):c.6034dup (p.Ser2012fs) | BRCA2 | Pathogenic | 13 | 32914522 | 32914523 | C | CT | reviewed by expert panel | ClinGen:CA645509064 |
Duplication | NM_000059.4(BRCA2):c.6611dup (p.Val2205fs) | BRCA2 | Pathogenic | 13 | 32915101 | 32915102 | T | TC | reviewed by expert panel | ClinGen:CA645372980 |
Duplication | NM_000059.4(BRCA2):c.7829dup (p.Asp2611fs) | BRCA2 | Pathogenic | 13 | 32936682 | 32936683 | G | GT | reviewed by expert panel | ClinGen:CA645509331 |
Deletion | NM_000059.4(BRCA2):c.8090_8105del (p.Ser2697fs) | BRCA2 | Pathogenic | 13 | 32937426 | 32937441 | TTGAGCGCAAATATATC | T | reviewed by expert panel | ClinGen:CA645509332 |
Duplication | NM_000059.4(BRCA2):c.8396dup (p.Pro2800fs) | BRCA2 | Pathogenic | 13 | 32944602 | 32944603 | A | AG | reviewed by expert panel | ClinGen:CA645509334 |
Deletion | NC_000017.11:g.(43047704_43049120)_(43049195_43051062)del | BRCA1 | Pathogenic | 17 | 41199721 | 41203079 | na | na | criteria provided, single submitter | - |
Deletion | NC_000017.10:g.(41219713_41222944)_(41267797_41276033)del | BRCA1 | Pathogenic | 17 | 41219713 | 41276033 | na | na | criteria provided, single submitter | - |
Duplication | NC_000017.10:g.(41228632_41234420)_(41234593_41242960)dup | BRCA1 | Pathogenic | 17 | 41228632 | 41242960 | na | na | criteria provided, single submitter | - |