Varaico: Literature-Extracted Genetic Variants

Gene:RUNX1
Variant:p.S167fs
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RUNX1

NM_001754.5:p.S167fs

Associated Papers

Clinical features, mutational landscape and their prognostic impact in Chinese paediatric patients with T-cell lymphoblastic lymphoma.

Li Y et al.

British Journal of Haematology, 2025

40958529 (PubMed )
Supplement: supplement_1.zip › Table_S3.xlsx › Sheet1

Searching for germline mutations in the RUNX1 gene among Polish patients with acute myeloid leukemia.

Bąk A et al.

Leukemia & Lymphoma, 2021

Distinctive phenotypes in two children with novel germline RUNX1 mutations - one with myeloid malignancy and increased fetal hemoglobin.

Bagla S et al.

Pediatric Hematology and Oncology, 2021

How I curate: applying American Society of Hematology-Clinical Genome Resource Myeloid Malignancy Variant Curation Expert Panel rules for RUNX1 variant curation for germline predisposition to myeloid malignancies.

Wu D et al.

Haematologica, 2020

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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."