Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NM_007294.4(BRCA1):c.4784del (p.Ser1595fs) | BRCA1 | Pathogenic | 17 | 41223147 | 41223147 | AG | A | reviewed by expert panel | ClinGen:CA10589644 |
Insertion | NM_007294.4(BRCA1):c.4758_4759insA (p.Ser1587fs) | BRCA1 | Pathogenic | 17 | 41223172 | 41223173 | A | AT | reviewed by expert panel | ClinGen:CA10589645 |
Deletion | NM_007294.4(BRCA1):c.4743del (p.Asp1582fs) | BRCA1 | Pathogenic | 17 | 41223188 | 41223188 | CT | C | reviewed by expert panel | ClinGen:CA10589646 |
Indel | NM_007294.4(BRCA1):c.4700_4710delinsA (p.Gly1567fs) | BRCA1 | Pathogenic | 17 | 41223221 | 41223231 | GAGGCTGATTC | T | reviewed by expert panel | ClinGen:CA10589647 |
Deletion | NM_007294.4(BRCA1):c.4699_4708del (p.Gly1567fs) | BRCA1 | Pathogenic | 17 | 41223223 | 41223232 | AGGCTGATTCC | A | reviewed by expert panel | ClinGen:CA10589648 |
Duplication | NM_007294.4(BRCA1):c.4688dup (p.Tyr1563Ter) | BRCA1 | Pathogenic | 17 | 41223242 | 41223243 | G | GT | reviewed by expert panel | ClinGen:CA10589649 |
Duplication | NM_007294.4(BRCA1):c.4668dup (p.Asp1557fs) | BRCA1 | Pathogenic | 17 | 41226354 | 41226355 | C | CT | reviewed by expert panel | ClinGen:CA10589650 |
Indel | NM_007294.4(BRCA1):c.4618_4621delinsAAA (p.Glu1540fs) | BRCA1 | Pathogenic | 17 | 41226402 | 41226405 | CTTC | TTT | reviewed by expert panel | ClinGen:CA10589652 |
Duplication | NM_007294.4(BRCA1):c.4593dup (p.Val1532fs) | BRCA1 | Pathogenic | 17 | 41226429 | 41226430 | C | CA | reviewed by expert panel | ClinGen:CA10589653 |
Deletion | NM_007294.4(BRCA1):c.4591del (p.Val1531fs) | BRCA1 | Pathogenic | 17 | 41226432 | 41226432 | AC | A | reviewed by expert panel | ClinGen:CA10589654 |