Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Duplication | NM_000059.4(BRCA2):c.7187dup (p.Leu2396fs) | BRCA2 | Pathogenic | 13 | 32929175 | 32929176 | C | CT | reviewed by expert panel | ClinGen:CA024940 |
single nucleotide variant | NM_000059.4(BRCA2):c.71T>A (p.Leu24Ter) | BRCA2 | Pathogenic | 13 | 32893217 | 32893217 | T | A | reviewed by expert panel | ClinGen:CA024957 |
Deletion | NM_000059.4(BRCA2):c.71del (p.Asp23_Leu24insTer) | BRCA2 | Pathogenic | 13 | 32893215 | 32893215 | AT | A | reviewed by expert panel | ClinGen:CA024955 |
Indel | NM_000059.4(BRCA2):c.7210_7216delinsTG (p.Lys2404fs) | BRCA2 | Pathogenic | 13 | 32929200 | 32929206 | AAAGTCT | TG | reviewed by expert panel | ClinGen:CA024964 |
Deletion | NM_000059.4(BRCA2):c.7211_7212del (p.Lys2404fs) | BRCA2 | Pathogenic | 13 | 32929200 | 32929201 | CAA | C | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):7439&base_change=del AA,ClinGen:CA024966 |
Deletion | NM_000059.4(BRCA2):c.7224_7227del (p.Pro2409fs) | BRCA2 | Pathogenic | 13 | 32929214 | 32929217 | CACCT | C | reviewed by expert panel | ClinGen:CA024972 |
Deletion | NM_000059.4(BRCA2):c.7226del (p.Pro2409fs) | BRCA2 | Pathogenic | 13 | 32929215 | 32929215 | AC | A | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):7454&base_change=del C,ClinGen:CA024977 |
Insertion | NM_000059.4(BRCA2):c.7234_7235insG (p.Thr2412fs) | BRCA2 | Pathogenic | 13 | 32929224 | 32929225 | A | AG | reviewed by expert panel | ClinGen:CA024981 |
single nucleotide variant | NM_000059.4(BRCA2):c.7241C>G (p.Ser2414Ter) | BRCA2 | Pathogenic | 13 | 32929231 | 32929231 | C | G | reviewed by expert panel | ClinGen:CA024987 |
single nucleotide variant | NM_000059.4(BRCA2):c.7261C>T (p.Gln2421Ter) | BRCA2 | Pathogenic | 13 | 32929251 | 32929251 | C | T | reviewed by expert panel | ClinGen:CA025004 |