databases > DOI:10.25504/FAIRsharing.Q7gFA9
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ready MitImpact

General Information
MitImpact is a collection of genomic, clinical, and functional annotations for all nucleotide changes that cause non-synonymous substitutions in human mitochondrial protein-coding genes

Homepage https://mitimpact.css-mendel.it/

Countries that developed this resource Italy

Created in 2015

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How to cite this record FAIRsharing.org: MitImpact; MitImpact; DOI: https://doi.org/10.25504/FAIRsharing.Q7gFA9; Last edited: Jan. 25, 2021, 4:28 p.m.; Last accessed: Aug 03 2021 2:42 a.m.

Publication for citation  High-confidence assessment of functional impact of human mitochondrial non-synonymous genome variations by APOGEE Castellana S, Fusilli C, Mazzoccoli G, Biagini T, Capocefalo D, Carella M, Vescovi AL, Mazza T.; PLoS Comput Biol ; 2017; 10.1371/journal.pcbi.1005628;


This record is maintained by irongraft

Record added: Oct. 15, 2020, 7:40 p.m.
Record updated: Oct. 20, 2020, 12:09 p.m. by The FAIRsharing Team.

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Support

General

online documentation Description
online documentation Legend of the output

Additional Information

Contact Tommaso Mazza   ORCID

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Conditions of Use


Data Versioning

MitImpact 3.0.6 No link recorded

Data Access

Search https://mitimpact.css-mendel.it/
Download No link recorded



Publications

MitImpact: an exhaustive collection of pre-computed pathogenicity predictions of human mitochondrial non-synonymous variants

Castellana S, Rónai J, Mazza T.
Hum Mutat. 2015

View Paper (PubMed) View Publication

High-confidence assessment of functional impact of human mitochondrial non-synonymous genome variations by APOGEE

Castellana S, Fusilli C, Mazzoccoli G, Biagini T, Capocefalo D, Carella M, Vescovi AL, Mazza T.
PLoS Comput Biol 2017

View Paper (PubMed) View Publication

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