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Article

Prediction of deleterious nonsynonymous single-nucleotide polymorphism for human diseases.

TheScientificWorldJournal - 1 Jan 2013

Wu Jiaxin, Jiang Rui

Abstract excerpt

The identification of genetic variants that are responsible for human inherited diseases is a fundamental problem in human and medical genetics. As a typical type of genetic variation, nonsynonymous single-nucleotide polymorphisms (nsSNPs) occurring in protein coding regions may alter the encoded amino acid, potentially affect protein structure and function, and further result in human inherited diseases....

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Identifiers

PMID: 23431257
DOI: 10.1155/2013/675851
PMCID: PMC3572689

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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