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. 2023 Nov 2;13(12):jkad227. doi: 10.1093/g3journal/jkad227

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© The Author(s) 2023. Published by Oxford University Press on behalf of The Genetics Society of America.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 1. — The workflow for variant assessment. The workflow of the current study is displayed. Caenorhabditis elegans and human variants for IFT140 were gathered from the indicated resources along with relevant info, such as allele frequency and clinical significance. Following the discovery of matching (equivalent) variants (MatchVars) and distinct variants, mutants bearing a missense or a stop codon were obtained from the CGC, or MatchVars were produced using the CRISPR/Cas9 genome editing tool.