rs148924904
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome.
|
18685109 |
2008 |
rs148924904
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
Germline mutations of the p53 tumor suppressor gene in children with osteosarcoma.
|
8164043 |
1994 |
rs148924904
|
|
C |
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 |
rs148924904
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
High frequency of de novo mutations in Li-Fraumeni syndrome.
|
19556618 |
2009 |
rs148924904
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes.
|
21343334 |
2011 |
rs148924904
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
Prevalence and functional consequence of TP53 mutations in pediatric adrenocortical carcinoma: a children's oncology group study.
|
25584008 |
2015 |
rs148924904
|
|
C |
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 |
rs148924904
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
Rapid detection of genetic mutations in individual breast cancer patients by next-generation DNA sequencing.
|
25757876 |
2015 |
rs148924904
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.
|
21601526 |
2011 |
rs148924904
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients.
|
11051239 |
2000 |
rs148924904
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography.
|
17392385 |
2007 |
rs148924904
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |