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Differences between alleles underlying QTL can vary from single nucleotide substitutions to large insertions or deletions between parental cultivars (Paran and Zamir 2003).
There are many different activities that work directly on DNA and bring about genetic changes, ranging from single nucleotide substitutions to major restructuring of chromosomes.
These included 581 HCDiffs with 417 single nucleotide substitutions, 411 homoplasmic and 6 heteroplasmic variants (Table 2 and Table S1).
Sequence variations included 15 single nucleotide substitutions, 6 of which are novel, and 1 novel small (tri-nucleotide) deletion.
Our results showed that 454 sequencing was comparable to Sanger sequencing in the detection of single nucleotide substitutions.
A total of 31 variable sites were found across the three H. merope subspecies, all single nucleotide substitutions.
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Sensitivity was assessed by comparing the results of competition experiments against TEV-PC1 of 24 single-nucleotide substitutions mutants.
Here, we report that both base editor 3 (BE3) using nCas9 and SaKKH-BE3 using SaKKH-nCas9 can introduce single-nucleotide substitutions efficiently in human tripronuclear (3PN) zygotes.
The majority (63.6%) of these mutations corresponded to single-nucleotide substitutions (missense and nonsense mutations).
Excluding the insertion, only six single-nucleotide substitutions were observed between the three 23S rRNA genes.
DJ-1 mutations are single-nucleotide substitutions or deletions leading to a non-functional protein [21], [22].
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