rs1060500126
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1064793345
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Lifetime cancer risks in individuals with germline PTEN mutations.
|
22252256 |
2012 |
rs1064793345
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Estimate of de novo mutation frequency in probands with PTEN hamartoma tumor syndrome.
|
22595938 |
2012 |
rs1114167640
|
|
CGCTT |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1554825530
|
|
ACT |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1554898083
|
|
CT |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1554898085
|
|
TCAAAC |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs370795352
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs398123317
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs587782350
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells.
|
27477328 |
2017 |
rs587782350
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
In vivo functional analysis of the counterbalance of hyperactive phosphatidylinositol 3-kinase p110 catalytic oncoproteins by the tumor suppressor PTEN.
|
17942903 |
2007 |
rs587782350
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes.
|
21828076 |
2011 |
rs587782350
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.
|
10400993 |
1999 |
rs587782350
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Characteristic brain magnetic resonance imaging pattern in patients with macrocephaly and PTEN mutations.
|
24375884 |
2014 |
rs587782350
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Elevated plasma succinate in PTEN, SDHB, and SDHD mutation-positive individuals.
|
22261759 |
2012 |
rs587782350
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults.
|
14566704 |
2003 |
rs587782350
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs863224909
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1085308041
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
|
28677221 |
2017 |
rs1085308043
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
|
28677221 |
2017 |
rs1114167621
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
|
28677221 |
2017 |
rs1114167622
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
|
28677221 |
2017 |
rs1114167650
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
|
28677221 |
2017 |
rs121909218
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909219
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|