rs28934874
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Clinical characteristics and registry-validated extended pedigrees of germline TP53 mutation carriers in Denmark.
|
29324801 |
2018 |
rs28934874
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.
|
25503501 |
2015 |
rs28934874
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Serine substitution of proline at codon 151 of TP53 confers gain of function activity leading to anoikis resistance and tumor progression of head and neck cancer cells.
|
23625637 |
2013 |
rs28934874
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Clinical relevance of gain-of-function mutations of p53 in high-grade serous ovarian carcinoma.
|
23967324 |
2013 |
rs28934874
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes.
|
21343334 |
2011 |
rs28934874
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes.
|
21343334 |
2011 |
rs28934874
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Analysis of the DNA-binding activity of p53 mutants using functional protein microarrays and its relationship to transcriptional activation.
|
20128691 |
2010 |
rs28934874
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Inactive full-length p53 mutants lacking dominant wild-type p53 inhibition highlight loss of heterozygosity as an important aspect of p53 status in human cancers.
|
16861262 |
2007 |
rs28934874
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Tumour p53 mutations exhibit promoter selective dominance over wild type p53.
|
11896595 |
2002 |
rs28934874
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Complex functions of mutant p53 alleles from human prostate cancer.
|
11920959 |
2002 |
rs28934874
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: further evidence of CHK2 in inherited cancer predisposition.
|
11479205 |
2001 |
rs28934874
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: further evidence of CHK2 in inherited cancer predisposition.
|
11479205 |
2001 |
rs28934874
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
TP53 gene mutations and 17p deletions in human astrocytomas.
|
1686725 |
1991 |