rs121909219
|
|
Type 1 Papillary Renal Cell Carcinoma
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121909219
|
|
Thyroid Nodule
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121909219
|
|
Pten Hamartoma Tumor Syndrome With Granular Cell Tumor
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121909219
|
|
PTEN Hamartoma Tumor Syndrome
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.
|
9140396 |
1997 |
rs121909219
|
|
PTEN Hamartoma Tumor Syndrome
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Cognitive characteristics of PTEN hamartoma tumor syndromes.
|
23470840 |
2013 |
rs121909219
|
|
PTEN Hamartoma Tumor Syndrome
|
T |
0.700 |
CausalMutation
|
CLINVAR |
A novel mutation of the PTEN gene in a Japanese patient with Cowden syndrome and bilateral breast cancer.
|
18558293 |
2008 |
rs121909219
|
|
PTEN Hamartoma Tumor Syndrome
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Mutation analysis of the PTEN / MMAC1 gene in Japanese patients with Cowden disease.
|
10920277 |
2000 |
rs121909219
|
|
PTEN Hamartoma Tumor Syndrome
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Cowden syndrome-related mutations in PTEN associate with enhanced proteasome activity.
|
23475934 |
2013 |
rs121909219
|
|
PTEN Hamartoma Tumor Syndrome
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutations.
|
24778394 |
2014 |
rs121909219
|
|
PTEN Hamartoma Tumor Syndrome
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations.
|
21956414 |
2011 |
rs121909219
|
|
PTEN Hamartoma Tumor Syndrome
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Germline mutations in PTEN are present in Bannayan-Zonana syndrome.
|
9241266 |
1997 |
rs121909219
|
|
Proteus-Like Syndrome (disorder)
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121909219
|
|
Poor school performance
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121909219
|
|
Penile freckling
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121909219
|
|
Papillary thyroid carcinoma
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121909219
|
|
ovarian neoplasm
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121909219
|
|
Non-Small Cell Lung Carcinoma
|
T |
0.700 |
CausalMutation
|
CLINVAR |
PTEN mutations and relationship to EGFR, ERBB2, KRAS, and TP53 mutations in non-small cell lung cancers.
|
20018398 |
2010 |
rs121909219
|
|
Non-Small Cell Lung Carcinoma
|
T |
0.700 |
CausalMutation
|
CLINVAR |
PTEN loss contributes to erlotinib resistance in EGFR-mutant lung cancer by activation of Akt and EGFR.
|
19351834 |
2009 |
rs121909219
|
|
Non-Small Cell Lung Carcinoma
|
T |
0.700 |
CausalMutation
|
CLINVAR |
The PI3K pathway as drug target in human cancer.
|
20085938 |
2010 |
rs121909219
|
|
Non-Small Cell Lung Carcinoma
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Enhanced sensitivity of PTEN-deficient tumors to inhibition of FRAP/mTOR.
|
11504908 |
2001 |
rs121909219
|
|
Non-Small Cell Lung Carcinoma
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Somatic mutations in epidermal growth factor receptor signaling pathway genes in non-small cell lung cancers.
|
20881644 |
2010 |
rs121909219
|
|
Non-Small Cell Lung Carcinoma
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Crystal structure of the PTEN tumor suppressor: implications for its phosphoinositide phosphatase activity and membrane association.
|
10555148 |
1999 |
rs121909219
|
|
Non-Small Cell Lung Carcinoma
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Inactivation of the PTEN/MMAC1/TEP1 gene in human lung cancers.
|
9598803 |
1998 |
rs121909219
|
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Mutation analysis of the PTEN / MMAC1 gene in Japanese patients with Cowden disease.
|
10920277 |
2000 |
rs121909219
|
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.
|
9140396 |
1997 |