Identifying Oncogenic Missense Single Nucleotide Polymorphisms in Human SAT1 Gene Using Computational Algorithms and Molecular Dynamics Tools.

Md Mozibullah Marina KhatunMd Asaduzzaman SikderMohammod Johirul IslamMehbuba Sharmin

Published in: Cancer reports (Hoboken, N.J.) (2024)

Therefore, the I21N variant was identified and concluded to be an oncogenic missense variant of the human SAT1 gene. Overall, the findings of this study would be a great directory of future experimental research to develop personalized medicine.

Keyphrases

molecular dynamics
endothelial cells
induced pluripotent stem cells
genome wide
intellectual disability
copy number
density functional theory
pluripotent stem cells
transcription factor
autism spectrum disorder
gene expression
current status