Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_024675.4(PALB2):c.48+2T>G | PALB2 | Likely pathogenic | 16 | 23652429 | 23652429 | A | C | criteria provided, single submitter | ClinGen:CA10580057 |
Deletion | NM_024675.4(PALB2):c.35del (p.Glu12fs) | PALB2 | Pathogenic | 16 | 23652444 | 23652444 | CT | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA10580061 |
Deletion | NM_007294.4(BRCA1):c.5328del (p.Thr1777fs) | BRCA1 | Pathogenic | 17 | 41203084 | 41203084 | TG | T | reviewed by expert panel | ClinGen:CA10580487 |
Deletion | NM_007294.4(BRCA1):c.5236del (p.His1746fs) | BRCA1 | Pathogenic | 17 | 41209110 | 41209110 | TG | T | reviewed by expert panel | ClinGen:CA10580492 |
Deletion | NM_007294.4(BRCA1):c.5202del (p.Phe1734fs) | BRCA1 | Pathogenic | 17 | 41209144 | 41209144 | CA | C | reviewed by expert panel | ClinGen:CA10580494 |
Deletion | NM_007294.4(BRCA1):c.5176del (p.Arg1726fs) | BRCA1 | Pathogenic | 17 | 41215367 | 41215367 | CT | C | reviewed by expert panel | ClinGen:CA10580497 |
single nucleotide variant | NM_007294.4(BRCA1):c.5135G>A (p.Trp1712Ter) | BRCA1 | Pathogenic | 17 | 41215908 | 41215908 | C | T | reviewed by expert panel | ClinGen:CA10580498 |
Duplication | NM_007294.4(BRCA1):c.4997dup (p.Tyr1666Ter) | BRCA1 | Pathogenic | 17 | 41219701 | 41219702 | G | GT | reviewed by expert panel | ClinGen:CA10580503 |
Deletion | NM_007294.4(BRCA1):c.4654_4673del (p.Tyr1552fs) | BRCA1 | Pathogenic | 17 | 41226350 | 41226369 | TAGATCTTGCCTTGGCAAGTA | T | reviewed by expert panel | ClinGen:CA10580512 |
single nucleotide variant | NM_007294.4(BRCA1):c.4432G>T (p.Glu1478Ter) | BRCA1 | Pathogenic | 17 | 41228557 | 41228557 | C | A | reviewed by expert panel | ClinGen:CA10580519 |