Varaico: Literature-Extracted Genetic Variants

Gene:RUNX1
Variant:p.S172G
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RUNX1

NM_001754.5:p.S172G

Associated Papers

Salivary gland cancer organoids are valid for preclinical genotype-oriented medical precision trials.

Ishikawa T et al.

Iscience, 2023

37207275 (PubMed )
Supplement: mmc7.xlsx › Sheet1

Single-Nucleotide Variations, Insertions/Deletions and Copy Number Variations in Myelodysplastic Syndrome during Disease Progression Revealed by a Single-Cell DNA Sequencing Platform.

Lee P et al.

International Journal of Molecular Sciences, 2022

35563039 (PubMed )
Supplement: ijms-23-04647-s001.zip › Supplemental_file_S5.xlsx › Supp_Table_S3

High frequency of germline RUNX1 mutations in patients with RUNX1-mutated AML.

Simon L et al.

Blood, 2020

RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML.

Brown AL et al.

Blood Advances, 2020

Chemogenomic Landscape of RUNX1-mutated AML Reveals Importance of RUNX1 Allele Dosage in Genetics and Glucocorticoid Sensitivity.

Simon L et al.

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

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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."