Varaico: Literature-Extracted Genetic Variants

Gene:SRC
Variant:p.R388W
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SRC

NM_198291.3:p.R388W

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

41386885 (PubMed )
Supplement: mmc6.xlsx › Sheet1

Small SNPs, Big Effects: A Review of Single Nucleotide Variations and Polymorphisms in Key Genes Associated With Autism Spectrum Disorder.

Srinath S et al.

International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience, 2025

Diabesity: New Candidate Genes and Structural and Functional Effects of Non-Synonymous Single Nucleotide Polymorphisms Identified by Computational Biology.

Kumar N et al.

Omics : a Journal of Integrative Biology, 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."