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Bioinformcrtics Analysis for Coding SNPs of the HLA-DQA1 Gene Involved in Susceptibility to Cervical Cancer

机译:HLA-DQA1基因编码SNP参与宫颈癌易感性的生物信息学分析

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OBJECTIVE To analyze coding SNPs of the HLA-DQA1 gene involved in susceptibility for cervical cancer by a bioinformatics approach, and to choose some SNPs that may have an association with cervical cancer. METHODS By a SNPper tool we extracted SNPs from a public database (dbSNP), exporting them in FASTA formats suitable for subsequent use. Then we used PARSESNP as a tool for the analysis of the cSNPs. RESULTS In the cSNPs of the HLA-DQA1 gene, we find that rs9272693 and rs9272703, are made up of missense mutations which convert a codon for one amino acid into a codon for a different amino acid. We chose a PSSM Difference >10 as a lower level for the scores of changes predicted to be deldterious. CONCLUSION We used a bioinformatics approach for cSNPs analysis of the HLA-DQA1 gene. This method can select the variants in a conserved region, and give a PSSM Difference score. But the results need to be verified in cervical cancer patients and a control population.
机译:目的通过生物信息学方法分析与宫颈癌易感性有关的HLA-DQA1基因的编码SNP,并选择一些可能与宫颈癌有关的SNP。方法我们使用SNPper工具从公共数据库(dbSNP)中提取了SNP,并以适合以后使用的FASTA格式导出了它们。然后,我们使用PARSESNP作为分析cSNP的工具。结果在HLA-DQA1基因的cSNP中,我们发现rs9272693和rs9272703由错义突变组成,这些错义突变将一个氨基酸的密码子转换为另一氨基酸的密码子。我们选择PSSM差异> 10作为较低级别,以预测变化的分数。结论我们使用生物信息学方法对HLA-DQA1基因进行cSNPs分析。该方法可以选择保守区域中的变体,并给出PSSM差异评分。但是结果需要在子宫颈癌患者和对照组人群中进行验证。

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