Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NM_007294.4(BRCA1):c.3285del (p.Lys1095fs) | BRCA1 | Pathogenic | 17 | 41244263 | 41244263 | GT | G | reviewed by expert panel | ClinGen:CA002117 |
single nucleotide variant | NM_007294.4(BRCA1):c.3286C>T (p.Gln1096Ter) | BRCA1 | Pathogenic | 17 | 41244262 | 41244262 | G | A | reviewed by expert panel | ClinGen:CA002118 |
Deletion | NM_007294.4(BRCA1):c.3286del (p.Gln1096fs) | BRCA1 | Pathogenic | 17 | 41244262 | 41244262 | TG | T | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):3405&base_change=del C,ClinGen:CA002119 |
Deletion | NM_007294.4(BRCA1):c.3288_3289del (p.Leu1098fs) | BRCA1 | Pathogenic | 17 | 41244259 | 41244260 | CTT | C | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):3407&base_change=del AA,ClinGen:CA002121 |
Deletion | NM_007294.4(BRCA1):c.3289del (p.Ser1097fs) | BRCA1 | Pathogenic | 17 | 41244259 | 41244259 | CT | C | reviewed by expert panel | ClinGen:CA002123 |
Deletion | NM_007294.4(BRCA1):c.3292_3293del (p.Leu1098fs) | BRCA1 | Pathogenic | 17 | 41244255 | 41244256 | AAG | A | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):3411&base_change=del CT,ClinGen:CA002124 |
Deletion | NM_007294.4(BRCA1):c.3296del (p.Pro1099fs) | BRCA1 | Pathogenic | 17 | 41244252 | 41244252 | AG | A | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):3415&base_change=del C,ClinGen:CA002128 |
Deletion | NM_007294.4(BRCA1):c.329_330del (p.Lys110fs) | BRCA1 | Pathogenic | 17 | 41256250 | 41256251 | CCT | C | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):448&base_change=del AG,ClinGen:CA002125 |
Duplication | NM_007294.4(BRCA1):c.329dup (p.Glu111fs) | BRCA1 | Pathogenic | 17 | 41256250 | 41256251 | C | CT | reviewed by expert panel | ClinGen:CA002126,Breast Cancer Information Core (BIC) (BRCA1):448&base_change=ins A |
Insertion | NM_007294.4(BRCA1):c.32_33insC (p.Gln12fs) | BRCA1 | Pathogenic | 17 | 41276081 | 41276082 | T | TG | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):151&base_change=ins C,ClinGen:CA002093 |