Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NM_000059.4(BRCA2):c.8959_8962del (p.Leu2987fs) | BRCA2 | Pathogenic | 13 | 32953891 | 32953894 | TACTG | T | reviewed by expert panel | ClinGen:CA10589533 |
Deletion | NM_000059.4(BRCA2):c.8965del (p.Ile2989fs) | BRCA2 | Pathogenic | 13 | 32953898 | 32953898 | TA | T | reviewed by expert panel | ClinGen:CA10589534 |
Insertion | NM_000059.4(BRCA2):c.8986_8987insAGAT (p.Leu2996Ter) | BRCA2 | Pathogenic | 13 | 32953918 | 32953919 | T | TTAGA | reviewed by expert panel | ClinGen:CA10589535 |
Deletion | NM_000059.4(BRCA2):c.8993_9024del (p.Ser2998fs) | BRCA2 | Pathogenic | 13 | 32953923 | 32953954 | TATTCTCTGTTAACAGAAGGAAAGAGATACAGA | T | reviewed by expert panel | ClinGen:CA10589536 |
Duplication | NM_000059.4(BRCA2):c.9017dup (p.Tyr3006Ter) | BRCA2 | Pathogenic | 13 | 32953949 | 32953950 | T | TA | reviewed by expert panel | ClinGen:CA10589537 |
Insertion | NM_000059.4(BRCA2):c.9019_9020insTCTA (p.Arg3007delinsIleTer) | BRCA2 | Pathogenic | 13 | 32953951 | 32953952 | C | CATCT | reviewed by expert panel | ClinGen:CA10589538 |
Deletion | NM_000059.4(BRCA2):c.9024_9046del (p.Ile3008_Tyr3009insTer) | BRCA2 | Pathogenic | 13 | 32953954 | 32953976 | GAATTTATCATCTTGCAACTTCAA | G | reviewed by expert panel | ClinGen:CA10589539 |
Duplication | NM_000059.4(BRCA2):c.9025dup (p.Tyr3009fs) | BRCA2 | Pathogenic | 13 | 32953955 | 32953956 | A | AT | reviewed by expert panel | ClinGen:CA10589540 |
Duplication | NM_000059.4(BRCA2):c.9034dup (p.Ala3012fs) | BRCA2 | Pathogenic | 13 | 32953966 | 32953967 | T | TG | reviewed by expert panel | ClinGen:CA10589541 |
Deletion | NM_000059.4(BRCA2):c.9052del (p.Ser3018fs) | BRCA2 | Pathogenic | 13 | 32953982 | 32953982 | TA | T | reviewed by expert panel | ClinGen:CA10589542 |