Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_007294.4(BRCA1):c.122A>G (p.His41Arg) | BRCA1 | Pathogenic | 17 | 41267755 | 41267755 | T | C | reviewed by expert panel | BRCA1-HCI:BRCA1_00130,ClinGen:CA000805 |
Deletion | NM_007294.4(BRCA1):c.122del (p.His41fs) | BRCA1 | Pathogenic | 17 | 41267755 | 41267755 | GT | G | reviewed by expert panel | ClinGen:CA000806 |
Deletion | NM_007294.4(BRCA1):c.1232_1233del (p.Asp411fs) | BRCA1 | Pathogenic | 17 | 41246315 | 41246316 | CAT | C | reviewed by expert panel | ClinGen:CA000808 |
Deletion | NM_007294.4(BRCA1):c.1240_1246del (p.Leu413_Asp414insTer) | BRCA1 | Pathogenic | 17 | 41246302 | 41246308 | AGAACGTC | A | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):1359&base_change=del GACGTTC,ClinGen:CA000815 |
Duplication | NM_007294.4(BRCA1):c.1241dup (p.Asp414fs) | BRCA1 | Pathogenic | 17 | 41246306 | 41246307 | G | GT | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):1360&base_change=ins A,ClinGen:CA000817 |
Deletion | NM_007294.4(BRCA1):c.124del (p.Ile42fs) | BRCA1 | Pathogenic | 17 | 41267753 | 41267753 | AT | A | reviewed by expert panel | ClinGen:CA000821,Breast Cancer Information Core (BIC) (BRCA1):243&base_change=del A |
single nucleotide variant | NM_007294.4(BRCA1):c.1252G>T (p.Glu418Ter) | BRCA1 | Pathogenic | 17 | 41246296 | 41246296 | C | A | reviewed by expert panel | ClinGen:CA000825 |
Deletion | NM_007294.4(BRCA1):c.1255del (p.Glu418_Val419insTer) | BRCA1 | Pathogenic | 17 | 41246293 | 41246293 | AC | A | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):1374&base_change=del G,ClinGen:CA000827 |
Duplication | NM_007294.4(BRCA1):c.1265dup (p.Tyr422Ter) | BRCA1 | Pathogenic | 17 | 41246282 | 41246283 | A | AT | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):1384&base_change=ins A,ClinGen:CA000834 |
single nucleotide variant | NM_007294.4(BRCA1):c.1266T>G (p.Tyr422Ter) | BRCA1 | Pathogenic | 17 | 41246282 | 41246282 | A | C | reviewed by expert panel | ClinGen:CA000836 |