Article

Synonymous SNP: Rare versus frequent codon can cause Phenotypic changes in the human genome

2019-03-20

Abstract excerpt

<h4>ABSTRACT</h4> Since the initial sequencing of the human genome, many projects are underway to understand the effects of genetic variation and phenotypic changes between individuals. Single nucleotide polymorphisms (SNPs) are an increasingly important tool for genetic and biomedical research. Synonymous Single Nucleotide Polymorphisms (sSNP) is an important source of human genome variability. It does not produ...

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Literature Corpus work: a2fb7d96-535c-5a46-b157-52b42484fcfa
DOI: 10.1101/582213

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