Varaico: Literature-Extracted Genetic Variants

Gene:RET
Variant:p.T636M
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RET

NM_020975.6:p.T636M

Associated Papers

Prioritization of predisposition genes for familial non-medullary thyroid cancer by whole-genome sequencing.

Srivastava A et al.

European Journal of Endocrinology, 2025

Understanding the variant landscape, and genetic epidemiology of Multiple Endocrine Neoplasia in India.

Vatsyayan A et al.

Endocrine, 2024

Identifying Lymph Node Metastasis-Related Factors in Breast Cancer Using Differential Modular and Mutational Structural Analysis.

Liu X et al.

Interdisciplinary Sciences, Computational Life Sciences, 2023

RET-Altered Cancers-A Tumor-Agnostic Review of Biology, Diagnosis and Targeted Therapy Activity.

Desilets A et al.

Cancers, 2023

Looking for RET alterations in thyroid cancer: clinical relevance, methodology and timing.

Elisei R et al.

Endocrine, 2023

An integrative pan cancer analysis of RET aberrations and their potential clinical implications.

Zhou L et al.

Scientific Reports, 2022

35978072 (PubMed )
Supplement: 41598_2022_17791_MOESM3_ESM.xlsx › table

GLOBAL ENDOCRINOLOGY: Geographical variation in the profile of RET variants in patients with medullary thyroid cancer: a comprehensive review.

Maciel RMB et al.

European Journal of Endocrinology, 2021

Early identification of disease progression in ALK-rearranged lung cancer using circulating tumor DNA analysis.

Angeles AK et al.

Npj Precision Oncology, 2021

34876698 (PubMed )
Supplement: 41698_2021_239_MOESM1_ESM.pdf

Oncogenic and drug-sensitive RET mutations in human epithelial ovarian cancer.

Guan L et al.

Journal of Experimental & Clinical Cancer Research : Cr, 2020

Ret Receptor Has Distinct Alterations and Functions in Breast Cancer.

Gattelli A et al.

Journal of Mammary Gland Biology and Neoplasia, 2020

A semiautomated whole-exome sequencing workflow leads to increased diagnostic yield and identification of novel candidate variants.

Ji J et al.

Cold Spring Harbor Molecular Case Studies, 2019

Broad Phenotypes of Disorders/Differences of Sex Development in MAMLD1 Patients Through Oligogenic Disease.

Flück CE et al.

Frontiers in Genetics, 2019

RET rearrangements are actionable alterations in breast cancer.

Paratala BS et al.

Nature Communications, 2018

RET Aberrations in Diverse Cancers: Next-Generation Sequencing of 4,871 Patients.

Kato S et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2017

27683183 (PubMed )
Supplement: 10780432ccr161679-sup-168576_1_supp_3636667_wcc1ns.docx

Diversity of mutations in the RET proto-oncogene and its oncogenic mechanism in medullary thyroid cancer.

Hedayati M et al.

Critical Reviews in Clinical Laboratory Sciences, 2016

Molecular Heterogeneity of Ewing Sarcoma as Detected by Ion Torrent Sequencing.

Zhang N et al.

Plos One, 2016

27077911 (PubMed )
Supplement: pone.0153546.s004.xlsx › Sheet1

Mutational Analysis of BRAF Inhibitor-Associated Squamoproliferative Lesions.

Clynick B et al.

The Journal of Molecular Diagnostics : Jmd, 2015

Identification and characterization of two novel germline RET variants associated with medullary thyroid carcinoma.

Silva AL et al.

Endocrine, 2015

Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility.

Toledo RA et al.

Endocrine-related Cancer, 2015

25425582 (PubMed )
Supplement: supp_ERC-14-0491_Supplementary_table_2.xlsx › Sheet1
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