Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Insertion | NM_007294.4(BRCA1):c.71_72insA (p.Cys24Ter) | BRCA1 | Pathogenic | 17 | 41276042 | 41276043 | A | AT | reviewed by expert panel | - |
Insertion | NM_007294.4(BRCA1):c.67_68insC (p.Glu23fs) | BRCA1 | Pathogenic | 17 | 41276046 | 41276047 | T | TG | reviewed by expert panel | - |
Duplication | NM_007294.4(BRCA1):c.34dup (p.Gln12fs) | BRCA1 | Pathogenic | 17 | 41276079 | 41276080 | T | TG | reviewed by expert panel | - |
Duplication | NM_007294.4(BRCA1):c.20dup (p.Val8fs) | BRCA1 | Pathogenic | 17 | 41276093 | 41276094 | G | GC | reviewed by expert panel | - |
Duplication | NM_000059.4(BRCA2):c.1062dup (p.Val355fs) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32906674 | 32906675 | A | AT | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000059.4(BRCA2):c.3767del (p.His1256fs) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32912259 | 32912259 | CA | C | criteria provided, multiple submitters, no conflicts | - |
Insertion | NM_000059.4(BRCA2):c.4624_4625insCG (p.Val1542fs) | BRCA2 | Likely pathogenic | 13 | 32913115 | 32913116 | A | AGC | criteria provided, single submitter | - |
Insertion | NM_000059.4(BRCA2):c.5216_5217insAATA (p.Tyr1739Ter) | BRCA2 | Likely pathogenic | 13 | 32913706 | 32913707 | T | TTAAA | criteria provided, single submitter | - |
Indel | NM_000059.4(BRCA2):c.5803delinsTT (p.Asn1935fs) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32914295 | 32914295 | A | TT | criteria provided, multiple submitters, no conflicts | - |
Insertion | NM_000059.4(BRCA2):c.6712_6713insGG (p.Asp2238fs) | BRCA2 | Likely pathogenic | 13 | 32915203 | 32915204 | T | TGG | criteria provided, single submitter | - |