rs137853077
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome.
|
9760200 |
1998 |
rs137853077
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients.
|
12372054 |
2002 |
rs137853077
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromes.
|
15987703 |
2005 |
rs137853077
|
|
C |
0.810 |
GeneticVariation |
CLINVAR |
LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromes.
|
15987703 |
2005 |
rs137853077
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families.
|
10408777 |
1999 |
rs137853077
|
|
C |
0.810 |
CausalMutation |
CLINVAR |
|
|
|
rs137853077
|
|
C |
0.810 |
GeneticVariation |
CLINVAR |
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
|
9428765 |
1998 |
rs137853077
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
|
9428765 |
1998 |
rs137853077
|
|
C |
0.810 |
GeneticVariation |
CLINVAR |
Genotype-phenotype correlations in Peutz-Jeghers syndrome.
|
15121768 |
2004 |
rs137853077
|
|
|
0.810 |
GeneticVariation |
BEFREE |
Effects of Peutz-Jeghers syndrome (PJS) causing missense mutations L67P, L182P, G242V and R297S on the structural dynamics of LKB1 (Liver kinase B1) protein.
|
29447078 |
2019 |
rs137853077
|
|
C |
0.810 |
GeneticVariation |
CLINVAR |
Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.
|
9887330 |
1999 |
rs137853077
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity.
|
9837816 |
1998 |
rs137853077
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.
|
9425897 |
1998 |
rs137853077
|
|
C |
0.810 |
GeneticVariation |
CLINVAR |
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity.
|
9837816 |
1998 |
rs137853077
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A novel de novo mutation in LKB1 gene in a Chinese Peutz Jeghers syndrome patient significantly diminished p53 activity.
|
21411391 |
2011 |