rs730881979
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
rs730881979
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
|
25394175 |
2015 |
rs730881979
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
|
25645574 |
2015 |
rs121913315
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Use of aromatase inhibitors in large cell calcifying sertoli cell tumors: effects on gynecomastia, growth velocity, and bone age.
|
25226294 |
2014 |
rs730881979
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Novel and recurrent mutations of STK11 gene in six Chinese cases with Peutz-Jeghers syndrome.
|
24604241 |
2014 |
rs730881979
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.
|
24652667 |
2014 |
rs1057520042
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |
rs121913315
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Pancreatic cancer risk in Peutz-Jeghers syndrome patients: a large cohort study and implications for surveillance.
|
23240097 |
2013 |
rs121913315
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.
|
23718779 |
2013 |
rs121913315
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Prevalence of germline PTEN, BMPR1A, SMAD4, STK11, and ENG mutations in patients with moderate-load colorectal polyps.
|
23399955 |
2013 |
rs137853082
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |
rs730881979
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |
rs1057520042
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel de novo mutation in LKB1 gene in a Chinese Peutz Jeghers syndrome patient significantly diminished p53 activity.
|
21411391 |
2011 |
rs121913315
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel de novo mutation in LKB1 gene in a Chinese Peutz Jeghers syndrome patient significantly diminished p53 activity.
|
21411391 |
2011 |
rs121913315
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
mTOR inhibitor treatment of pancreatic cancer in a patient With Peutz-Jeghers syndrome.
|
21189378 |
2011 |
rs137853082
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel de novo mutation in LKB1 gene in a Chinese Peutz Jeghers syndrome patient significantly diminished p53 activity.
|
21411391 |
2011 |
rs121913315
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Alu-mediated genomic deletion of the serine/threonine protein kinase 11 (STK11) gene in Peutz-Jeghers syndrome.
|
20435009 |
2010 |
rs121913315
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Structure of the LKB1-STRAD-MO25 complex reveals an allosteric mechanism of kinase activation.
|
19892943 |
2009 |
rs730881979
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates.
|
17924967 |
2007 |
rs121913315
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.
|
16582077 |
2006 |
rs121913315
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus.
|
17026623 |
2006 |
rs1057520042
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromes.
|
15987703 |
2005 |
rs121913315
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromes.
|
15987703 |
2005 |
rs121913315
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
|
16287113 |
2005 |
rs137853082
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromes.
|
15987703 |
2005 |