Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Duplication | NM_007294.4(BRCA1):c.1227_1230dup (p.Asp411delinsSerTer) | BRCA1 | Pathogenic | 17 | 41246317 | 41246318 | C | CAGCT | reviewed by expert panel | ClinGen:CA10589957 |
single nucleotide variant | NM_007294.4(BRCA1):c.1222A>T (p.Lys408Ter) | BRCA1 | Pathogenic | 17 | 41246326 | 41246326 | T | A | reviewed by expert panel | ClinGen:CA10589958 |
Insertion | NM_007294.4(BRCA1):c.1210_1211insCT (p.Glu404fs) | BRCA1 | Pathogenic | 17 | 41246337 | 41246338 | T | TAG | reviewed by expert panel | ClinGen:CA10589959 |
Deletion | NM_007294.4(BRCA1):c.1209_1210del (p.Glu404fs) | BRCA1 | Pathogenic | 17 | 41246338 | 41246339 | TCA | T | reviewed by expert panel | ClinGen:CA10589960 |
Duplication | NM_007294.4(BRCA1):c.1209dup (p.Glu404Ter) | BRCA1 | Pathogenic | 17 | 41246338 | 41246339 | C | CA | reviewed by expert panel | ClinGen:CA10589961 |
Insertion | NM_007294.4(BRCA1):c.1179_1180insT (p.Gly394fs) | BRCA1 | Pathogenic | 17 | 41246368 | 41246369 | C | CA | reviewed by expert panel | ClinGen:CA10589962 |
Deletion | NM_007294.4(BRCA1):c.1174del (p.Leu392fs) | BRCA1 | Pathogenic | 17 | 41246374 | 41246374 | AG | A | reviewed by expert panel | ClinGen:CA10589963 |
single nucleotide variant | NM_007294.4(BRCA1):c.1171G>T (p.Glu391Ter) | BRCA1 | Pathogenic | 17 | 41246377 | 41246377 | C | A | reviewed by expert panel | ClinGen:CA10589964 |
Deletion | NM_007294.4(BRCA1):c.1140del (p.Val382fs) | BRCA1 | Pathogenic | 17 | 41246408 | 41246408 | TC | T | reviewed by expert panel | ClinGen:CA10589965 |
Deletion | NM_007294.4(BRCA1):c.1125_1132del (p.Asn376fs) | BRCA1 | Pathogenic | 17 | 41246416 | 41246423 | CTGCTATTT | C | reviewed by expert panel | ClinGen:CA10589966 |