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. 2019 Feb 8;20:16. doi: 10.1186/s12863-019-0718-z

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© The Author(s). 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 7 — Schema of the Universal hGR database. Data from various sources are collected and curated to identify hGR variants. The analyzed information is assigned unique data tracking identifiers. The changes are appended to the reference hGR sequence, which may result in a revised nucleotide sequence. These changes are annotated with dynamically-adjusting UhGR location identifiers that allow the user to locate specific variants. The adjusted sequence is displayed on an Excel worksheet, along with the lists of variants