|
rs587782529
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |
|
rs587782529
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes.
|
21343334 |
2011 |
|
rs587782529
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
Altered-function p53 missense mutations identified in breast cancers can have subtle effects on transactivation.
|
20407015 |
2010 |
|
rs587782529
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
Analysis of the DNA-binding activity of p53 mutants using functional protein microarrays and its relationship to transcriptional activation.
|
20128691 |
2010 |
|
rs587782529
|
|
|
0.810 |
GeneticVariation |
BEFREE |
The novel somatic mutation, R337G (16900C>G), was discovered in myelodysplastic syndrome with transformation to acute myeloblastic leukemia, developing as the third primary in the LFS child.
|
19714490 |
2009 |
|
rs587782529
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
Transcriptional functionality of germ line p53 mutants influences cancer phenotype.
|
17606709 |
2007 |
|
rs587782529
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography.
|
17392385 |
2007 |
|
rs587782529
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
Penetrance of adrenocortical tumours associated with the germline TP53 R337H mutation.
|
16033918 |
2006 |
|
rs587782529
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
Understanding the function-structure and function-mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis.
|
12826609 |
2003 |
|
rs587782529
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
P53 germline mutations in childhood cancers and cancer risk for carrier individuals.
|
10864200 |
2000 |
|
rs587782529
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family.
|
10484981 |
1999 |
|
rs587782529
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A germline missense mutation R337C in exon 10 of the human p53 gene.
|
9452042 |
1998 |
|
rs587782529
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
Characterization of p53 oligomerization domain mutations isolated from Li-Fraumeni and Li-Fraumeni like family members.
|
9704930 |
1998 |
|
rs587782529
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
Characterization of the oligomerization defects of two p53 mutants found in families with Li-Fraumeni and Li-Fraumeni-like syndrome.
|
9704931 |
1998 |
|
rs587782529
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
Two functional assays employed to detect an unusual mutation in the oligomerisation domain of p53 in a Li-Fraumeni like family.
|
9150393 |
1997 |
|
rs587782529
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53.
|
8825920 |
1995 |
|
rs587782529
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Germ-line p53 mutations in 15 families with Li-Fraumeni syndrome.
|
7887414 |
1995 |
|
rs587782529
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Hereditary and acquired p53 gene mutations in childhood acute lymphoblastic leukemia.
|
1737852 |
1992 |
|
rs587782529
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms.
|
1565144 |
1992 |
|
rs587782529
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A germ line mutation in exon 5 of the p53 gene in an extended cancer family.
|
1933902 |
1991 |
|
rs587782529
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome.
|
2259385 |
1991 |
|
rs587782529
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms.
|
1978757 |
1990 |