Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NM_000059.4(BRCA2):c.9887del (p.Lys3296fs) | BRCA2 | Pathogenic | 13 | 32972536 | 32972536 | GA | G | criteria provided, single submitter | ClinGen:CA658798107 |
single nucleotide variant | NM_000059.4(BRCA2):c.9883C>T (p.Gln3295Ter) | BRCA2 | Pathogenic | 13 | 32972533 | 32972533 | C | T | reviewed by expert panel | ClinGen:CA026321 |
Deletion | NM_000059.4(BRCA2):c.9871del (p.Ser3291fs) | BRCA2 | Pathogenic | 13 | 32972519 | 32972519 | GT | G | reviewed by expert panel | ClinGen:CA10589577 |
Deletion | NM_000059.4(BRCA2):c.9868del (p.Val3290fs) | BRCA2 | Pathogenic | 13 | 32972518 | 32972518 | TG | T | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):10096&base_change=del G,ClinGen:CA026317 |
Deletion | NM_000059.4(BRCA2):c.9850_9866del (p.Ser3284fs) | BRCA2 | Likely pathogenic | 13 | 32972498 | 32972514 | GTTAGTCCCATTTGTACA | G | criteria provided, single submitter | - |
Duplication | NM_000059.4(BRCA2):c.9846dup (p.Val3283fs) | BRCA2 | Pathogenic | 13 | 32972495 | 32972496 | C | CT | reviewed by expert panel | ClinGen:CA10589576 |
single nucleotide variant | NM_000059.4(BRCA2):c.9836T>A (p.Leu3279Ter) | BRCA2 | Pathogenic | 13 | 32972486 | 32972486 | T | A | reviewed by expert panel | ClinGen:CA10589575 |
Deletion | NM_000059.4(BRCA2):c.9824del (p.Ser3275fs) | BRCA2 | Pathogenic | 13 | 32972474 | 32972474 | AG | A | reviewed by expert panel | ClinGen:CA026307 |
Duplication | NM_000059.4(BRCA2):c.9810dup (p.Asp3272fs) | BRCA2 | Pathogenic | 13 | 32972458 | 32972459 | G | GC | criteria provided, multiple submitters, no conflicts | ClinGen:CA658683837 |
Deletion | NM_000059.4(BRCA2):c.9808del (p.Ala3270fs) | BRCA2 | Pathogenic | 13 | 32972458 | 32972458 | AG | A | reviewed by expert panel | ClinGen:CA026301 |