|
rs28897759
|
|
Malignant neoplasm of breast
|
T |
0.810 |
GeneticVariation
|
CLINVAR |
|
|
|
|
rs28897759
|
|
Malignant neoplasm of breast
|
|
0.810 |
GeneticVariation
|
BEFREE |
We analyzed a missense VUS located in BRCA2 (p.Asn3124Ile; HGVS: BRCA2 c.9371A > T) present in seven independent high-risk breast cancer families that were counseled and genetically tested in South-West Germany.
|
24728577 |
2014 |
|
rs28897759
|
|
Malignant neoplasm of breast
|
|
0.810 |
GeneticVariation
|
UNIPROT |
|
|
|
|
rs80359014
|
|
Malignant neoplasm of breast
|
T |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
|
rs80359014
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
|
|
|
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors.
|
15604628 |
2004 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
BRCA2 gene mutations in families with aggregations of breast and stomach cancers.
|
12373604 |
2002 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
A low proportion of BRCA2 mutations in Finnish breast cancer families.
|
9150152 |
1997 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
An improved high throughput heteroduplex mutation detection system for screening BRCA2 mutations-fluorescent mutation detection (F-MD).
|
11241844 |
2001 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Somatic mutations in the BRCA2 gene and high frequency of allelic loss of BRCA2 in sporadic male breast cancer.
|
11948477 |
2002 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
BRCA1 and BRCA2 sequence variants in Chinese breast cancer families.
|
12442274 |
2002 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2.
|
16793542 |
2006 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families.
|
15026808 |
2004 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Frequency of BRCA1 and BRCA2 germline mutations in Japanese breast cancer families.
|
11149425 |
2001 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
BRCA2 T2722R is a deleterious allele that causes exon skipping.
|
12145750 |
2002 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Novel germline mutations in the BRCA1 and BRCA2 genes in Indian breast and breast-ovarian cancer families.
|
14722926 |
2004 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
T |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
BRCA1 and BRCA2 germline mutations in Korean patients with sporadic breast cancer.
|
15365993 |
2004 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Germline brca2 sequence variants in patients with ocular melanoma.
|
10399947 |
1999 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Hereditary breast and ovarian cancer in Cyprus: identification of a founder BRCA2 mutation.
|
15172753 |
2004 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
BRCA2 germline mutations in male breast cancer patients in the Polish population.
|
11139248 |
2001 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Summaries for patients. Assessing the genetic risk for BRCA-related breast or ovarian cancer in women: recommendations from the U.S. Preventive Services Task Force.
|
24366402 |
2014 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
High throughput fluorescence-based conformation-sensitive gel electrophoresis (F-CSGE) identifies six unique BRCA2 mutations and an overall low incidence of BRCA2 mutations in high-risk BRCA1-negative breast cancer families.
|
9654203 |
1998 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Global sequence diversity of BRCA2: analysis of 71 breast cancer families and 95 control individuals of worldwide populations.
|
9971877 |
1999 |
|
rs45580035
|
|
Malignant neoplasm of breast
|
|
0.800 |
GeneticVariation
|
UNIPROT |
BRCA2 germline mutations in familial pancreatic carcinoma.
|
12569143 |
2003 |