Varaico: Literature-Extracted Genetic Variants

Gene:SRC
Variant:p.R391C
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SRC

NM_198291.3:p.R391C

Associated Papers

Molecular insights of vitamin D receptor SNPs and vitamin D analogs: a novel therapeutic avenue for vitiligo.

Sundaravel SS et al.

Molecular Diversity, 2025

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

TSC angiofibroma and ungual fibroma have different mutation signatures, with recurrent mutations in KMT2C.

Klonowska K et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2025

Combined sequence and sequence-structure based methods for analyzing FGF23, CYP24A1 and VDR genes.

Nagamani S et al.

Meta Gene, 2016

The vitamin D receptor and the syndrome of hereditary 1,25-dihydroxyvitamin D-resistant rickets.

Malloy PJ et al.

Endocrine Reviews, 1999

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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."