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. 2021 Mar 30;11(6):jkab099. doi: 10.1093/g3journal/jkab099

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© The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://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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The average number of each SNV as it occurs in unique triplet nucleotide context is distinct between rnr1 alleles. Bars are colored according to the six different types of SNVs. (A) The 16 different triplet contexts are lettered for display purposes. The variant change (C>A, blue bar) occurs at the middle nucleotide marked X in each triplet context for (B) RNR1, (C) rnr1D57N, (D) rnr1Y285F pGAL-RNR1, (E) rnr1Y285F, (F) rnr1Y285A pGAL-RNR1, and (G) rnr1Y285A.

Note: Figure Replacement Requested.