|
rs80356923
|
|
|
0.710 |
GeneticVariation |
BEFREE |
Here, we report the first case of serous tubal intraepithelial carcinoma identified through a risk-reducing salpingo-oophorectomy in a Japanese woman with hereditary breast and ovarian cancer syndrome and who had a deleterious germline mutation of E1214X in BRCA1, but not a BRCA2 mutation.
|
24719479 |
2014 |
|
rs80356923
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Here, we report the first case of serous tubal intraepithelial carcinoma identified through a risk-reducing salpingo-oophorectomy in a Japanese woman with hereditary breast and ovarian cancer syndrome and who had a deleterious germline mutation of E1214X in BRCA1, but not a BRCA2 mutation.
|
24719479 |
2014 |
|
rs80356923
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Germline BRCA1 and BRCA2 mutations in ovarian cancer: utility of a histology-based referral strategy.
|
22776961 |
2012 |
|
rs80356923
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Diagnostic guidelines for high-resolution melting curve (HRM) analysis: an interlaboratory validation of BRCA1 mutation scanning using the 96-well LightScanner.
|
19370767 |
2009 |
|
rs80356923
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
The prevalence of BRCA1 and BRCA2 germline mutations in high-risk breast cancer patients of Chinese Han nationality: two recurrent mutations were identified.
|
17851763 |
2008 |
|
rs80356923
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
|
16683254 |
2006 |
|
rs80356923
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations.
|
16267036 |
2005 |
|
rs80356923
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Frequency of BRCA1 and BRCA2 germline mutations in Japanese breast cancer families.
|
11149425 |
2001 |
|
rs80356923
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Molecular profiles of BRCA1-mutated and matched sporadic breast tumours: relation with clinico-pathological features.
|
11506493 |
2001 |
|
rs80356923
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families.
|
9150151 |
1997 |
|
rs80356923
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Mutations in the BRCA1 gene in Japanese breast cancer patients.
|
8723683 |
1996 |