|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
GeneticVariation
|
disease |
CLINVAR |
The effects of genomic germline variant reclassification on clinical cancer care.
|
30728895 |
2019 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
CausalMutation
|
disease |
CLINVAR |
Pathogenic Germline Variants in 10,389 Adult Cancers.
|
29625052 |
2018 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
GeneticVariation
|
disease |
CLINVAR |
Inherited Breast Cancer in Nigerian Women.
|
30130155 |
2018 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
CausalMutation
|
disease |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
CausalMutation
|
disease |
CLINVAR |
Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.
|
26786923 |
2016 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
GeneticVariation
|
disease |
CLINVAR |
Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells.
|
25646469 |
2015 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
CausalMutation
|
disease |
CLINVAR |
Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer.
|
26315354 |
2015 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
GeneticVariation
|
disease |
CLINVAR |
Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer.
|
26315354 |
2015 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
GeneticVariation
|
disease |
CLINVAR |
Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel.
|
25186627 |
2015 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
GeneticVariation
|
disease |
CLINVAR |
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
|
25980754 |
2015 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
CausalMutation
|
disease |
CLINVAR |
Integrated analysis of germline and somatic variants in ovarian cancer.
|
24448499 |
2014 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
CausalMutation
|
disease |
CLINVAR |
Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients.
|
24763289 |
2014 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
CausalMutation
|
disease |
CLINVAR |
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles.
|
17033622 |
2006 |
|
| Entrez Id: |
83990 |
| Gene Symbol: |
BRIP1 |
BRIP1
|
0.410 |
CausalMutation
|
disease |
CLINVAR |
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
|
16116423 |
2005 |