rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.
31131967
2019
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
A comprehensive focus on global spectrum of BRCA1 and BRCA2 mutations in breast cancer.
24312913
2013
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants.
22505045
2012
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
Detection of BRCA1/2 mutations in breast cancer patients from Thailand and Pakistan.
22486713
2012
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell-based assay.
21719596
2011
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
A high proportion of DNA variants of BRCA1 and BRCA2 is associated with aberrant splicing in breast/ovarian cancer patients.
20215541
2010
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
Spectrum and characterisation of BRCA1 and BRCA2 deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer.
18489799
2008
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
Functional assays for classification of BRCA2 variants of uncertain significance.
18451181
2008
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.
17924331
2007
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
A missense mutation in exon 13 in BRCA2, c.7235G>A, results in skipping of exon 13.
16792514
2006
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
Inherited FANCD1/BRCA2 exon 7 splice mutations associated with acute myeloid leukaemia in Fanconi anaemia D1 are not found in sporadic childhood leukaemia.
16115142
2005
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families.
15026808
2004
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A
0.700
CausalMutation
CLINVAR
Biallelic inactivation of BRCA2 in Fanconi anemia.
12065746
2002
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
T
0.700
CausalMutation
CLINVAR
rs28897743
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
C
0.700
CausalMutation
CLINVAR