rs80358755
|
|
|
0.710 |
GeneticVariation |
BEFREE |
Nevertheless, comprehensive studies of mutation G1770V in large series of BC patients from Morocco are needed to assess the real prevalence of this mutation and to improve genetic testing and risk assessment in this population.
|
26864382 |
2016 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2.
|
16793542 |
2006 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families.
|
15026808 |
2004 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Hereditary breast and ovarian cancer in Cyprus: identification of a founder BRCA2 mutation.
|
15172753 |
2004 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Novel germline mutations in the BRCA1 and BRCA2 genes in Indian breast and breast-ovarian cancer families.
|
14722926 |
2004 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
BRCA1 and BRCA2 germline mutations in Korean patients with sporadic breast cancer.
|
15365993 |
2004 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
BRCA2 germline mutations in familial pancreatic carcinoma.
|
12569143 |
2003 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Twenty-three novel BRCA1 and BRCA2 sequence alterations in breast and/or ovarian cancer families in Southern Germany.
|
12938098 |
2003 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
BRCA2 T2722R is a deleterious allele that causes exon skipping.
|
12145750 |
2002 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
BRCA1 and BRCA2 sequence variants in Chinese breast cancer families.
|
12442274 |
2002 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Somatic mutations in the BRCA2 gene and high frequency of allelic loss of BRCA2 in sporadic male breast cancer.
|
11948477 |
2002 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
BRCA2 gene mutations in families with aggregations of breast and stomach cancers.
|
12373604 |
2002 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
BRCA2 germline mutations in male breast cancer patients in the Polish population.
|
11139248 |
2001 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
An improved high throughput heteroduplex mutation detection system for screening BRCA2 mutations-fluorescent mutation detection (F-MD).
|
11241844 |
2001 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Frequency of BRCA1 and BRCA2 germline mutations in Japanese breast cancer families.
|
11149425 |
2001 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
BRCA2 germline mutations among early onset breast cancer patients unselected for family history of the disease.
|
10978364 |
2000 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Germline brca2 sequence variants in patients with ocular melanoma.
|
10399947 |
1999 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Global sequence diversity of BRCA2: analysis of 71 breast cancer families and 95 control individuals of worldwide populations.
|
9971877 |
1999 |
rs80358755
|
|
|
0.710 |
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 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
High proportion of missense mutations of the BRCA1 and BRCA2 genes in Japanese breast cancer families.
|
9609997 |
1998 |
rs80358755
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
A low proportion of BRCA2 mutations in Finnish breast cancer families.
|
9150152 |
1997 |