Varaico: Literature-Extracted Genetic Variants

Gene:DDX10
Variant:p.D788del1
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DDX10

NM_004398.4:p.D788del1

Associated Papers

DDX10 RNA Helicase: Structure, Function, and Oncogenic Roles Across Solid and Hematologic Tumors.

Isinelli G et al.

Genes, 2026

Genetic landscape of myelodysplastic syndrome and its prognostic relevance: a study from Pakistan.

Waheed A et al.

Jpma. the Journal of the Pakistan Medical Association, 2025

Identification of DHX40 as a candidate susceptibility gene for colorectal and hematological neoplasia.

Olkinuora A et al.

Leukemia, 2023

37696923 (PubMed )
Supplement: 41375_2023_2021_MOESM10_ESM.xlsx › Table_S5

Integrated genetic and epigenetic analysis reveals DNA repair alterations in multifocal hepatocellular carcinoma.

Ling YH et al.

Signal Transduction and Targeted Therapy, 2023

37349321 (PubMed )
Supplement: 41392_2023_1446_MOESM2_ESM.xlsx › Sheet_1

Dendritic Spine in Autism Genetics: Whole-Exome Sequencing Identifying De Novo Variant of CTTNBP2 in a Quad Family Affected by Autism Spectrum Disorder.

Xie Y et al.

Children (basel, Switzerland), 2022

36670631 (PubMed )
Supplement: children-10-00080-s001.zip › children-2044403-supplementary › children-2044403-Supplementary › Supplementary_Tables-R1.xlsx › STS5

Whole-Exome Sequencing Reveals Clinical Potential of Circulating Tumor DNA from Peritoneal Fluid and Plasma in Endometrial Cancer.

Ju HY et al.

Cancers, 2022

35626111 (PubMed )
Supplement: cancers-14-02506-s001.zip › Supplementary_Tables.xlsx › Supplementary_Table_S2

Spred-3 mutation and Ras/Raf/MAPK activation confer acquired resistance to EGFR tyrosine kinase inhibitor in an EGFR mutated NSCLC cell line.

He Z et al.

Translational Cancer Research, 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."