Varaico: Literature-Extracted Genetic Variants

Gene:TERT
Variant:p.P380S
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TERT

NM_198253.3:p.P380S

Associated Papers

Mutation characteristics of cancer susceptibility genes in Chinese ovarian cancer patients.

Wang J et al.

Frontiers in Oncology, 2024

38817903 (PubMed )
Supplement: Table_3.xlsx › Sheet1

TP53 mutations identify high-risk events for peripheral T-cell lymphoma treated with CHOP-based chemotherapy.

Johnson WT et al.

Blood Advances, 2023

37078708 (PubMed )
Supplement: BLOODA_ADV-2023-009953-mmc1.xlsx › S10J_MEITL_mutations

TERT Mutations in Non-Small Cell Lung Cancer: Clinicopathologic Features and Prognostic Implications.

Yang L et al.

Clinical Medicine Insights. Oncology, 2023

A Vietnamese human genetic variation database.

Le VS et al.

Human Mutation, 2019

Targeted next-generation sequencing in papillary thyroid carcinoma patients looking for germline variants predisposing to the disease.

Shen CT et al.

Endocrine, 2019

Granular cell astrocytoma: an aggressive IDH-wildtype diffuse glioma with molecular genetic features of primary glioblastoma.

Vizcaino MA et al.

Brain Pathology (zurich, Switzerland), 2019

Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs.

Li N et al.

Breast Cancer Research : Bcr, 2018

29316957 (PubMed )
Supplement: 13058_2017_929_MOESM1_ESM.xlsx › Table_S3

[Clinical and genetic features of dyskeratosis congenital with bone marrow failure in eight patients].

Wan Y et al.

Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2016

Telomerase mutation: a genetic risk factor for cirrhosis.

Chaiteerakij R et al.

Hepatology (baltimore, Md.), 2011

Telomerase gene mutations are associated with cirrhosis formation.

Hartmann D et al.

Hepatology (baltimore, Md.), 2011

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."