Barely Significant
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Compound and heterozygous mutations of KCNQ1 in long QT syndrome with familial history of unexplained sudden death: Identified by analysis of whole exome sequencing and predisposing genes.

Ann Noninvasive Electrocardiol · 2020 · PMC7358849 · PMID 31565860

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an increasing trendno p-value reported
5.3 Protein physics and chemical parameters prediction Predicted by the ProtParam tool, it can be seen that compared with the wild type, the Theoretical pI, Instability index, Aliphatic index, and Grand average of hydropathicity (GRAVY) of W176X showed an increasing trend.

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