2026-04-142026-04-142025ROZA, Gustavo Ronconi et al. In silico evaluation of effect and molecular modeling of snps in genes related to amyotrophic lateral sclerosis. Sclerosis, Basel, v. 3, n. 3, e27, 2025. DOI: 10.3390/sclerosis3030027. Disponível em: https://www.mdpi.com/2813-3064/3/3/27. Acesso em: 9 abr. 2026.e- 2813-3064https://repositorio.bc.ufg.br//handle/ri/30095Background: Amyotrophic lateral sclerosis is a systemic, complex, multifactorial, and fatal neurodegenerative disease with various factors involved in its etiology. This study aimed to understand the effects of SNPs in the MTHFR, MTR, SLC19A1, and VAPB genes on protein functionality and structure and their influence on ALS susceptibility. Methods: The dbSNP and ClinVar databases were used for SNP data annotation, while UniProt and PDB provided protein sequences. We performed functional and structural predictions of SNPs using PolyPhen-2 and SNAP2. We modeled mutant proteins using AlphaFold 2 and visualized them in PyMOL to compare native and mutant forms. Results: Our results identified SNP rs74315431 as pathogenic, inducing structural and functional changes and exhibiting visible alterations in the three-dimensional structure. Although predicted as non-pathogenic, SNPs rs1801131, rs1805087, and rs1051266 caused protein structural alterations, a finding confirmed by three-dimensional visualization. SNP rs1801133 diverged from the others, being predicted as pathogenic but without causing changes in protein structure or function. Conclusions: Our study found a strong correlation between SNAP2-predicted alterations and those predicted by AlphaFold 2, whereas PolyPhen-2 results did not directly correlate with three-dimensional structure changes.engAcesso Abertohttp://creativecommons.org/licenses/by-nc-nd/4.0/NeurodegenerationHyperhomocysteinemiaMembrane contact sitesComputa- tional analysisProtein structural perturbationArtigo10.3390/sclerosis3030027