Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Somatic mutations in the BRCA1 gene in sporadic ovarian tumours. 7795652

1995
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. 7894493

1994
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Human BRCA1 inhibits growth in yeast: potential use in diagnostic testing. 9159158

1997
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR The cancer-predisposing mutation C61G disrupts homodimer formation in the NH2-terminal BRCA1 RING finger domain. 9525870

1998
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer. 10788334

2000
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR BRCA1 physically and functionally interacts with ATF1. 10945975

2000
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR The RING heterodimer BRCA1-BARD1 is a ubiquitin ligase inactivated by a breast cancer-derived mutation. 11278247

2001
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Cancer-predisposing mutations within the RING domain of BRCA1: loss of ubiquitin protein ligase activity and protection from radiation hypersensitivity. 11320250

2001
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age. 11389159

2001
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics. 12601471

2003
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Binding and recognition in the assembly of an active BRCA1/BARD1 ubiquitin-ligase complex. 12732733

2003
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Contributions of ATM mutations to familial breast and ovarian cancer. 12810666

2003
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR BRCA1 : BARD1 induces the formation of conjugated ubiquitin structures, dependent on K6 of ubiquitin, in cells during DNA replication and repair. 14976165

2004
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR The BRCA1 RING and BRCT domains cooperate in targeting BRCA1 to ionizing radiation-induced nuclear foci. 15569676

2005
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague area. 16168118

2005
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Genetic analysis of BRCA1 ubiquitin ligase activity and its relationship to breast cancer susceptibility. 16403807

2006
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR A yeast recombination assay to characterize human BRCA1 missense variants of unknown pathological significance. 18680205

2009
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Characterization of BRCA1 ring finger variants of uncertain significance. 19543972

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Haplotype of the C61G BRCA1 mutation in Polish and Jewish individuals. 19594371

2009
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Identification of breast tumor mutations in BRCA1 that abolish its function in homologous DNA recombination. 20103620

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Occult ovarian cancers identified at risk-reducing salpingo-oophorectomy in a prospective cohort of BRCA1/2 mutation carriers. 20180014

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR The contribution of founder mutations in BRCA1 to breast and ovarian cancer in Lithuania. 20345474

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR The contribution of founder mutations in BRCA1 to breast cancer in Belarus. 20507347

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR High frequency and allele-specific differences of BRCA1 founder mutations in breast cancer and ovarian cancer patients from Belarus. 20569256

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 germline mutations screening in Algerian breast/ovarian cancer families. 20683152

2010