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Article

SNP2NMD: a database of human single nucleotide polymorphisms causing nonsense-mediated mRNA decay.

Bioinformatics (Oxford, England) - 1 Feb 2007

Han Areum, Kim Woo-Yeon, Park Seong-Min

Abstract excerpt

UNLABELLED: Elucidating the effects of genetic polymorphisms on genes and gene networks is an important step in disease association studies. We developed the SNP2NMD database for human SNPs (single nucleotide polymorphisms) that result in PTCs (premature termination codons) and trigger nonsense-mediated mRNA decay (NMD). The SNP2NMD Web interfaces provide extensive genetic information on and graphical views of...

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Identifiers

PMID: 17121775
DOI: 10.1093/bioinformatics/btl593

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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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