Varaico: Literature-Extracted Genetic Variants

Gene:RET
Variant:p.V591I
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RET

NM_020975.6:p.V591I

Associated Papers

Advancing Precision Oncology in Hereditary Paraganglioma-Pheochromocytoma Syndromes: Integrated Interpretation and Data Sharing of the Germline and Tumor Genomes.

Rana HQ et al.

Cancers, 2024

Role of tissue and circulating microRNAs and DNA as biomarkers in medullary thyroid cancer.

Chiacchiarini M et al.

Pharmacology & Therapeutics, 2021

Ret Receptor Has Distinct Alterations and Functions in Breast Cancer.

Gattelli A et al.

Journal of Mammary Gland Biology and Neoplasia, 2020

Molecular Genetics in the Diagnosis and Biology of Lymphoid Neoplasms.

Lim MS et al.

American Journal of Clinical Pathology, 2019

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

[Hereditary thyroid carcinoma and its molecular diagnostics].

Dvořáková S et al.

Ceskoslovenska Patologie, 2014

Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas.

Dvorakova S et al.

Molecular and Cellular Endocrinology, 2008

[Thyroid carcinomas and Hirschsprung's disease--10-year experience with molecular genetic testing of the RET proto-oncogene].

Bendlová B et al.

Vnitrni Lekarstvi, 2006

New multiple somatic mutations in the RET proto-oncogene associated with a sporadic medullary thyroid carcinoma.

Dvoráková S et al.

Thyroid : Official Journal of the American Thyroid Association, 2006

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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."