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SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants
Single nucleotide variants (SNVs) are, together with copy number variation, the primary source of variation in the human genome and are associated with phenotypic variation such as altered response to drug treatment and susceptibility to disease. Linking structural effects of non-synonymous SNVs to...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3245173/ https://ncbi.nlm.nih.gov/pubmed/22075996 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkr996 |
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