Varaico: Literature-Extracted Genetic Variants

Gene:JAK2
Variant:p.K385insFs
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JAK2

NM_004972.4:p.K385insFs

Associated Papers

Effects of CALR-Mutant Type and Burden on the Phenotype of Myeloproliferative Neoplasms.

Kim HY et al.

Diagnostics (basel, Switzerland), 2022

Integration of Molecular Information in Risk Assessment of Patients with Myeloproliferative Neoplasms.

Loscocco GG et al.

Cells, 2021

Impact of Mutational Profile on the Management of Myeloproliferative Neoplasms: A Short Review of the Emerging Data.

Loscocco GG et al.

Oncotargets and Therapy, 2020

Philadelphia-Negative Myeloproliferative Neoplasms: Laboratory Workup in the Era of Next-Generation Sequencing.

Zuo Z et al.

Current Hematologic Malignancy Reports, 2019

Clinical and Hematological Relevance of JAK2V617F, CALR, and MPL Mutations in Vietnamese Patients with Essential Thrombocythemia.

Vu HA et al.

Asian Pacific Journal of Cancer Prevention : Apjcp, 2019

Mayo CALR mutation type classification guide using alpha helix propensity.

Lasho TL et al.

American Journal of Hematology, 2018

Diagnostic, Prognostic, and Predictive Utility of Recurrent Somatic Mutations in Myeloid Neoplasms.

Patel U et al.

Clinical Lymphoma, Myeloma & Leukemia, 2017

Genetic Characteristics of Polycythemia Vera and Essential Thrombocythemia in Korean Patients.

Yoo EH et al.

Journal of Clinical Laboratory Analysis, 2016

Coexistence of JAK2 and CALR mutations and their clinical implications in patients with essential thrombocythemia.

Kang MG et al.

Oncotarget, 2016

JAK2, CALR, and MPL mutation spectrum in Japanese patients with myeloproliferative neoplasms.

Shirane S et al.

Haematologica, 2015

Calreticulin mutations and long-term survival in essential thrombocythemia.

Tefferi A et al.

Leukemia, 2014

Low rate of calreticulin mutations in refractory anaemia with ring sideroblasts and marked thrombocytosis.

Broséus J et al.

Leukemia, 2014

CALR gene mutational profile in myeloproliferative neoplasms with non-mutated JAK2 in Moroccan patients: A case series and germline in-frame deletion.

Smaili W et al.

Current Research in Translational Medicine, 0

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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."