Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Insertion | NM_007294.4(BRCA1):c.3110_3111insT (p.Lys1037fs) | BRCA1 | Pathogenic | 17 | 41244437 | 41244438 | T | TA | reviewed by expert panel | - |
Insertion | NM_007294.4(BRCA1):c.3054_3055insTGAGA (p.Ile1019Ter) | BRCA1 | Pathogenic | 17 | 41244493 | 41244494 | T | TTCTCA | reviewed by expert panel | - |
Insertion | NM_007294.4(BRCA1):c.2904_2905insTC (p.Asn969fs) | BRCA1 | Pathogenic | 17 | 41244643 | 41244644 | T | TGA | reviewed by expert panel | - |
Duplication | NM_007294.4(BRCA1):c.2903dup (p.Asn969fs) | BRCA1 | Pathogenic | 17 | 41244644 | 41244645 | T | TG | reviewed by expert panel | ClinGen:CA645373188 |
Insertion | NM_007294.4(BRCA1):c.2872_2873insA (p.Phe958fs) | BRCA1 | Pathogenic | 17 | 41244675 | 41244676 | A | AT | reviewed by expert panel | - |
Duplication | NM_007294.4(BRCA1):c.2866dup (p.Ser956fs) | BRCA1 | Pathogenic | 17 | 41244681 | 41244682 | G | GA | reviewed by expert panel | - |
Insertion | NM_007294.4(BRCA1):c.2851_2852insC (p.Arg951fs) | BRCA1 | Pathogenic | 17 | 41244696 | 41244697 | C | CG | reviewed by expert panel | - |
Insertion | NM_007294.4(BRCA1):c.2788_2789insTTATCACTGCAGGCTTT (p.Pro930fs) | BRCA1 | Pathogenic | 17 | 41244759 | 41244760 | G | GAAAGCCTGCAGTGATAA | reviewed by expert panel | - |
Insertion | NM_007294.4(BRCA1):c.2778_2779insAT (p.Ala927fs) | BRCA1 | Pathogenic | 17 | 41244769 | 41244770 | C | CAT | reviewed by expert panel | - |
Insertion | NM_007294.4(BRCA1):c.2755_2756insGGGTG (p.Pro919fs) | BRCA1 | Pathogenic | 17 | 41244792 | 41244793 | G | GCACCC | reviewed by expert panel | - |