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Mutations of short tandem repeat loci in cases of paternity testing in Chinese

机译:亲子鉴定中短串联重复基因座的突变

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摘要

In order to find out the characteristics of genetic mutations in 15 short tandem repeat (STR) loci, 3734 parentage cases were analyzed using AmpFlSTR Sinofiler kit. The allele source, mutation rate, and mutation rule of the STR loci were determined. Seventy mutations were observed in all cases for paternity testing. Among 15 STR loci, the highest mutation rate was observed in D12S391 (0.21 %), but the D5S818 gene mutation rate was relatively low (0.02 %). One-step mutation cases accounted for 95.7 % of all of the cases monitored. And the mutations in this study mainly showed paternal mutation (64/70). The research results are of great significance for identification and paternity tests and for the improvement of genetic studies on Chinese population in the future.
机译:为了找出15个短串联重复序列(STR)基因座的遗传突变特征,使用AmpFlSTR Sinofiler试剂盒分析了3734例亲子病例。确定了STR基因座的等位基因来源,突变率和突变规则。在所有情况下均观察到70个突变用于亲子鉴定。在15个STR位点中,D12S391的突变率最高(0.21%),而D5S818的基因突变率相对较低(0.02%)。单步突变病例占所有监测病例的95.7%。本研究中的突变主要表现为父系突变(64/70)。该研究结果对鉴定和亲子鉴定以及对未来中国人群遗传学研究的改进具有重要意义。

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