SNPeffect
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| Database name: | |
| Alternative name: | - |
| URL: | |
| Database maintenance site: | Switch Laboratory |
| Country/Region: | Belgium |
| Database description: | 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. |
| Organism(s) covered: | |
| Tag - Target: | Genome/Gene, Protein, Genetic variation, Health/Disease |
| Tag - Information type: | Sequence, Interaction/Pathway, Phenotype, 3D structure |
| Reference(s) - PubMed ID/DOI: | PubMed ID: DOI: PubMed ID: DOI: PubMed ID: DOI: PubMed ID: DOI: |
| Language(s): | English |
| Operational status: | Active |
| Link(s) to Downloadable data: | - |
| Link(s) to Metadata of downloadable data: | - |
| Link(s) to Terms of use: | - |
| Link(s) to "How to use": | - |
| Contact information of database: | - |
| Link(s) to API / SPARQL endpoint | - |
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Link to LSDB Archive:
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- |
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Link to MEDALS Database list:
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- |
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Link to TogoTV:
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- |
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Link to FAIRsharing:
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https://fairsharing.org/10.25504/FAIRsharing.qbt1gh |
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Similar databases:
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PolyDoms DisGeNET: a database of gene-disease associations PhenoModifier RNA Binding Protein Variant Database Mutation@A Glance AlloMAPS HmtVar PreMedKB IRView CancerSplicingQTL |
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Record maintainer
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See the corresponding part in the FAIRsharing record. |
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Record source:
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 (2018-12-21)
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Date of creation of this record:
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2019-03-28 |
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Last update date of this record:
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2020-07-09 |
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Record license:
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Creative Commons Attribution and Share-alike (CC-BY-SA) International 4.0 license |