Varaico: Literature-Extracted Genetic Variants

Gene:NOTCH1
Variant:p.S356F
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NOTCH1

NM_017617.5:p.S356F

Associated Papers

Somatic mutation and selection at population scale.

Lawson ARJ et al.

Nature, 2025

41062696 (PubMed )
Supplement: 41586_2025_9584_MOESM6_ESM.xlsx › clinvar_annotation

Ethnic-Specific and UV-Independent Mutational Signatures of Basal Cell Carcinoma in Koreans.

Kim YA et al.

International Journal of Molecular Sciences, 2025

40725190 (PubMed )
Supplement: ijms-26-06941-s001.zip › Supplementary_TableS2.xlsx › Only_in_Korean

Genomic progression for local invasion of cutaneous squamous cell carcinoma from the superficial to the deep portion.

Hwang HW et al.

International Journal of Cancer, 2024

Pathogenic Variants Associated with Epigenetic Control and the NOTCH Pathway Are Frequent in Classic Hodgkin Lymphoma.

Santisteban-Espejo A et al.

International Journal of Molecular Sciences, 2024

38473705 (PubMed )
Supplement: ijms-25-02457-s001.zip › ijms-2818045-supplementary.pdf

Somatic mutations in facial skin from countries of contrasting skin cancer risk.

King C et al.

Nature Genetics, 2023

37537257 (PubMed )
Supplement: 41588_2023_1468_MOESM3_ESM.xlsx › Supp_Table_1

Ultradeep sequencing differentiates patterns of skin clonal mutations associated with sun-exposure status and skin cancer burden.

Wei L et al.

Science Advances, 2021

33523857 (PubMed )
Supplement: abd7703_SM.pdf

Evaluating Cancer of the Central Nervous System Through Next-Generation Sequencing of Cerebrospinal Fluid.

Pentsova EI et al.

Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology, 2016

27161972 (PubMed )
Supplement: supp_JCO.2016.66.6487_DS_2016.666487.xlsx › SNV__Indels
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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."