Varaico: Literature-Extracted Genetic Variants

Gene:SRC
Variant:p.R388Q
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SRC

NM_198291.3:p.R388Q

Associated Papers

Bioinformatics-driven identification of pathogenic missense nsSNPs in the human proto-oncogene SRC and cancer susceptibility.

Ahamed MS et al.

Journal, Genetic Engineering & Biotechnology, 2025

In Silico Characterization of Pathogenic ESR2 Coding and UTR Variants as Oncogenic Potential Biomarkers in Hormone-Dependent Cancers.

Al-Nakhle H et al.

Genes, 2025

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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."