Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Duplication | NM_007294.4(BRCA1):c.3908_3909dup (p.Glu1304fs) | BRCA1 | Pathogenic | 17 | 41243638 | 41243639 | C | CCA | reviewed by expert panel | ClinGen:CA10589715 |
Indel | NM_007294.4(BRCA1):c.3907_3908delinsGGA (p.Leu1303fs) | BRCA1 | Pathogenic | 17 | 41243640 | 41243641 | AA | TCC | reviewed by expert panel | ClinGen:CA10589716 |
Deletion | NM_007294.4(BRCA1):c.3885del (p.Leu1295fs) | BRCA1 | Pathogenic | 17 | 41243663 | 41243663 | AC | A | reviewed by expert panel | ClinGen:CA10589717 |
single nucleotide variant | NM_007294.4(BRCA1):c.3862G>T (p.Glu1288Ter) | BRCA1 | Pathogenic | 17 | 41243686 | 41243686 | C | A | reviewed by expert panel | ClinGen:CA10589718 |
Duplication | NM_007294.4(BRCA1):c.3851_3852dup (p.Leu1285fs) | BRCA1 | Pathogenic | 17 | 41243695 | 41243696 | G | GGT | reviewed by expert panel | ClinGen:CA002481 |
Deletion | NM_007294.4(BRCA1):c.3840_3850del (p.Gln1281fs) | BRCA1 | Pathogenic | 17 | 41243698 | 41243708 | TGATGTTCCTGA | T | reviewed by expert panel | ClinGen:CA10589719 |
Deletion | NM_007294.4(BRCA1):c.3839_3843del (p.Ala1279_Ser1280insTer) | BRCA1 | Pathogenic | 17 | 41243705 | 41243709 | CCTGAG | C | reviewed by expert panel | ClinGen:CA10589720 |
Deletion | NM_007294.4(BRCA1):c.3837_3840del (p.Ser1280fs) | BRCA1 | Pathogenic | 17 | 41243708 | 41243711 | GAGAT | G | reviewed by expert panel | ClinGen:CA10589721 |
Duplication | NM_007294.4(BRCA1):c.3821dup (p.Ile1275fs) | BRCA1 | Pathogenic | 17 | 41243726 | 41243727 | T | TA | reviewed by expert panel | ClinGen:CA10589722 |
single nucleotide variant | NM_007294.4(BRCA1):c.3810C>A (p.Cys1270Ter) | BRCA1 | Pathogenic | 17 | 41243738 | 41243738 | G | T | reviewed by expert panel | ClinGen:CA10589723 |