|
rs587781288
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |
|
rs587781288
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Identification of new p53 target microRNAs by bioinformatics and functional analysis.
|
24256616 |
2013 |
|
rs587781288
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
A comprehensive study of TP53 mutations in chronic lymphocytic leukemia: Analysis of 1287 diagnostic and 1148 follow-up CLL samples.
|
21232794 |
2011 |
|
rs587781288
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes.
|
21343334 |
2011 |
|
rs587781288
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes.
|
20522432 |
2010 |
|
rs587781288
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Analysis of the DNA-binding activity of p53 mutants using functional protein microarrays and its relationship to transcriptional activation.
|
20128691 |
2010 |
|
rs587781288
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography.
|
17392385 |
2007 |
|
rs587781288
|
|
T |
0.800 |
CausalMutation |
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 |
|
rs587781288
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Understanding the function-structure and function-mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis.
|
12826609 |
2003 |
|
rs587781288
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome.
|
11370630 |
2001 |
|
rs587781288
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family.
|
10484981 |
1999 |
|
rs587781288
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Germline mutations of p53 but not p16/CDKN2 or PTEN/MMAC1 tumor suppressor genes predispose to gliomas. The ANOCEF Group. Association des NeuroOncologues d'Expression Française.
|
10589545 |
1999 |
|
rs587781288
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A germline missense mutation R337C in exon 10 of the human p53 gene.
|
9452042 |
1998 |
|
rs587781288
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53.
|
8825920 |
1995 |
|
rs587781288
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Germ-line p53 mutations in 15 families with Li-Fraumeni syndrome.
|
7887414 |
1995 |
|
rs587781288
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms.
|
1565144 |
1992 |
|
rs587781288
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Hereditary and acquired p53 gene mutations in childhood acute lymphoblastic leukemia.
|
1737852 |
1992 |
|
rs587781288
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A germ line mutation in exon 5 of the p53 gene in an extended cancer family.
|
1933902 |
1991 |
|
rs587781288
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome.
|
2259385 |
1991 |
|
rs587781288
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms.
|
1978757 |
1990 |