Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Duplication | NM_000059.4(BRCA2):c.6164dup (p.Ser2056fs) | BRCA2 | Pathogenic | 13 | 32914653 | 32914654 | C | CT | reviewed by expert panel | ClinGen:CA645372977 |
Insertion | NM_000059.4(BRCA2):c.6272_6273insA (p.Ser2091fs) | BRCA2 | Pathogenic | 13 | 32914764 | 32914765 | G | GA | reviewed by expert panel | - |
Insertion | NM_000059.4(BRCA2):c.6419_6420insA (p.Gly2141fs) | BRCA2 | Pathogenic | 13 | 32914911 | 32914912 | G | GA | reviewed by expert panel | - |
Insertion | NM_000059.4(BRCA2):c.6534_6535insA (p.Val2179fs) | BRCA2 | Pathogenic | 13 | 32915026 | 32915027 | T | TA | reviewed by expert panel | - |
Insertion | NM_000059.4(BRCA2):c.6662_6663insAAAG (p.Asn2221fs) | BRCA2 | Pathogenic | 13 | 32915154 | 32915155 | A | AAAAG | reviewed by expert panel | - |
Duplication | NM_000059.4(BRCA2):c.6723dup (p.Asp2242fs) | BRCA2 | Pathogenic | 13 | 32915214 | 32915215 | C | CA | reviewed by expert panel | - |
Insertion | NM_000059.4(BRCA2):c.6947_6948insTT (p.Lys2316fs) | BRCA2 | Pathogenic | 13 | 32920973 | 32920974 | A | ATT | reviewed by expert panel | - |
Insertion | NM_000059.4(BRCA2):c.7023_7024insTG (p.Gln2342fs) | BRCA2 | Pathogenic | 13 | 32929013 | 32929014 | T | TTG | reviewed by expert panel | - |
Insertion | NM_000059.4(BRCA2):c.7233_7234insG (p.Thr2412fs) | BRCA2 | Pathogenic | 13 | 32929223 | 32929224 | A | AG | reviewed by expert panel | - |
Deletion | NM_000059.4(BRCA2):c.7308del (p.Asn2436fs) | BRCA2 | Pathogenic | 13 | 32929298 | 32929298 | AC | A | reviewed by expert panel | - |