rs587782144
|
|
T |
0.810 |
GeneticVariation |
CLINVAR |
The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.
|
28349240 |
2017 |
rs587782144
|
|
T |
0.810 |
GeneticVariation |
CLINVAR |
TP53 Variations in Human Cancers: New Lessons from the IARC TP53 Database and Genomics Data.
|
27328919 |
2016 |
rs587782144
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
Prevalence and functional consequence of TP53 mutations in pediatric adrenocortical carcinoma: a children's oncology group study.
|
25584008 |
2015 |
rs587782144
|
|
T |
0.810 |
GeneticVariation |
CLINVAR |
Prevalence and functional consequence of TP53 mutations in pediatric adrenocortical carcinoma: a children's oncology group study.
|
25584008 |
2015 |
rs587782144
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
|
26014290 |
2015 |
rs587782144
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
Prevalence and functional consequence of TP53 mutations in pediatric adrenocortical carcinoma: a children's oncology group study.
|
25584008 |
2015 |
rs587782144
|
|
T |
0.810 |
GeneticVariation |
CLINVAR |
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
|
25741868 |
2015 |
rs587782144
|
|
T |
0.810 |
GeneticVariation |
CLINVAR |
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
|
26014290 |
2015 |
rs587782144
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
Lack of toxicity in a patient with germline TP53 mutation treated with radiotherapy.
|
24764719 |
2014 |
rs587782144
|
|
T |
0.810 |
GeneticVariation |
CLINVAR |
Lack of toxicity in a patient with germline TP53 mutation treated with radiotherapy.
|
24764719 |
2014 |
rs587782144
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |
rs587782144
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
Tongue carcinoma infrequently harbor common actionable genetic alterations.
|
25234657 |
2014 |
rs587782144
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
Prevalence of germline TP53 mutations in a prospective series of unselected patients with adrenocortical carcinoma.
|
23175693 |
2013 |
rs587782144
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
High frequency of germline TP53 mutations in a prospective adult-onset sarcoma cohort.
|
23894400 |
2013 |
rs587782144
|
|
T |
0.810 |
GeneticVariation |
CLINVAR |
Prevalence of germline TP53 mutations in a prospective series of unselected patients with adrenocortical carcinoma.
|
23175693 |
2013 |
rs587782144
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
High frequency of germline TP53 mutations in a prospective adult-onset sarcoma cohort.
|
23894400 |
2013 |
rs587782144
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
TP53 germline mutations in adult patients with adrenocortical carcinoma.
|
22170717 |
2012 |
rs587782144
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes.
|
21343334 |
2011 |
rs587782144
|
|
T |
0.810 |
GeneticVariation |
CLINVAR |
Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes.
|
21343334 |
2011 |
rs587782144
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
Multiple primary cutaneous melanomas in Li-Fraumeni syndrome.
|
21339461 |
2011 |
rs587782144
|
|
T |
0.810 |
GeneticVariation |
CLINVAR |
Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.
|
21601526 |
2011 |
rs587782144
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.
|
21601526 |
2011 |
rs587782144
|
|
T |
0.810 |
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 |
rs587782144
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
One index case with glioblastoma multiforme (GBM) diagnosed at age 54 and had a family history comprised of a paternal aunt with GBM at age 55, carried the p53 R158H mutation, which is predicted to be functional and has previously been implicated as a cause of Li-Fraumeni syndrome.
|
20455025 |
2010 |
rs587782144
|
|
|
0.810 |
GeneticVariation |
BEFREE |
One index case with glioblastoma multiforme (GBM) diagnosed at age 54 and had a family history comprised of a paternal aunt with GBM at age 55, carried the p53 R158H mutation, which is predicted to be functional and has previously been implicated as a cause of Li-Fraumeni syndrome.
|
20455025 |
2010 |