rs397507422
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Population and breast cancer patients' analysis reveals the diversity of genomic variation of the BRCA genes in the Mexican population.
|
30630528 |
2019 |
rs397507884
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mis-splicing in breast cancer: identification of pathogenic BRCA2 variants by systematic minigene assays.
|
30883759 |
2019 |
rs80358843
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
BRCA Reversion Mutations in Circulating Tumor DNA Predict Primary and Acquired Resistance to the PARP Inhibitor Rucaparib in High-Grade Ovarian Carcinoma.
|
30425037 |
2019 |
rs80359013
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
The functional impact of variants of uncertain significance in BRCA2.
|
29988080 |
2019 |
rs80359519
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Population and breast cancer patients' analysis reveals the diversity of genomic variation of the BRCA genes in the Mexican population.
|
30630528 |
2019 |
rs81002796
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mis-splicing in breast cancer: identification of pathogenic BRCA2 variants by systematic minigene assays.
|
30883759 |
2019 |
rs1466688245
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Genetic and clinical characteristics in Japanese hereditary breast and ovarian cancer: first report after establishment of HBOC registration system in Japan.
|
29176636 |
2018 |
rs1566249353
|
|
GA |
0.700 |
CausalMutation |
CLINVAR |
Genetic and clinical characteristics in Japanese hereditary breast and ovarian cancer: first report after establishment of HBOC registration system in Japan.
|
29176636 |
2018 |
rs276174843
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Intraductal/ductal histology and lymphovascular invasion are associated with germline DNA-repair gene mutations in prostate cancer.
|
29368341 |
2018 |
rs397507410
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs397507634
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs397507634
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Location of Mutation in BRCA2 Gene and Survival in Patients with Ovarian Cancer.
|
29084914 |
2018 |
rs397507634
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Inherited mutations in BRCA1 and BRCA2 in an unselected multiethnic cohort of Asian patients with breast cancer and healthy controls from Malaysia.
|
28993434 |
2018 |
rs397507683
|
|
GA |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.
|
29339979 |
2018 |
rs397507788
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs397507865
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs397507868
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs397507884
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs55996097
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs587782011
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs587782854
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.
|
29339979 |
2018 |
rs750385844
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Screening of over 1000 Indian patients with breast and/or ovarian cancer with a multi-gene panel: prevalence of BRCA1/2 and non-BRCA mutations.
|
29470806 |
2018 |
rs758732038
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Inherited mutations in BRCA1 and BRCA2 in an unselected multiethnic cohort of Asian patients with breast cancer and healthy controls from Malaysia.
|
28993434 |
2018 |
rs786201180
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Characterization of spliceogenic variants located in regions linked to high levels of alternative splicing: BRCA2 c.7976+5G > T as a case study.
|
29969168 |
2018 |
rs79728106
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |