By using Genedoc to compare the sequences of these 20 individuals, 54 variation sites were observed, of which 2 are of base deletion, 1 base insertion, 43 transition sites, 7 transversion sites and 2 transition-transversion sites.
用Genedoc软件进行序列比较，在这20个个体中，共检测到54个变异位点，包括：2个碱基缺失、1个碱基插入、43个转换位点、7个颠换位点及2个转换与颠换同时存在的位点。
参考来源 - 蓝点马鲛和日本鳀的遗传多样性研究·2,447,543篇论文数据，部分数据来源于NoteExpress
该序列一共具有34个分析性状（包括17个变异位点，9个位点碱基缺失）。
There were 34 analyzing characters could be used for analysis, including 17 transpositional loci and 9 missing ones.
在发生重排的T-DNA之间除了碱基缺失外，还发现存在填充序列和微同源序列。
Deletion of nucleotides, filler sequences and microhomology were found at junction of rearranged T-DNAs.
在检测到的24个碱基突变中，主要是碱基的置换(87.5%)，碱基缺失的比例比较小(12.5%)。
In all of the 24 bases of mutants, the base replacement occupies about 87.5% of the total mutants with only a small portion of gene deletion (12.5%).
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