ready SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants

Abbreviation:SNPeffect 4.0

General Information
SNPeffect is a database for phenotyping human single nucleotide polymorphisms (SNPs). SNPeffect primarily focuses on the molecular characterization and annotation of disease and polymorphism variants in the human proteome. Further, SNPeffect holds per-variant annotations on functional sites, structural features and post-translational modification.



Record updated: Sept. 14, 2016, 9:38 a.m. by The FAIRsharing Team.



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  • IUAP P6/43 (Federal Office for Scientific Affairs, Belgium)


Publications

SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs.

Reumers J., Schymkowitz J., Ferkinghoff-Borg J., Stricher F., Serrano L., Rousseau F.,
Nucleic Acids Res. 2005

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SNPeffect v2.0: a new step in investigating the molecular phenotypic effects of human non-synonymous SNPs.

Reumers J., Maurer-Stroh S., Schymkowitz J., Rousseau F.,
Bioinformatics 2006

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Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases.

Reumers J., Conde L., Medina I., Maurer-Stroh S., Van Durme J., Dopazo J., Rousseau F., Schymkowitz J.,
Nucleic Acids Res. 2008

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SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants.

De Baets G,Van Durme J,Reumers J,Maurer-Stroh S,Vanhee P,Dopazo J,Schymkowitz J,Rousseau F
Nucleic Acids Res 2011

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