These scripts were used in the analysis/classification of missense variants in X-linked genes, starting with CACNA1F gene. The variant properties from a functionaly benign dataset and pathogenic dataset were identifed and used in the classification/prediction of variants. Each script was used to extract a piece of information
shalawsallah/CACNA1F-variants-analysis
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this repository contains scripts used to analyse pathogenic and benign missense variants and their properties for a set of X-linked genes
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