PRP: Pathogenic Risk Prediction for Rare Nonsynonymous Single Nucleotide Variants

This repository contains the training dataset and three independent test datasets used in the study "PRP:Pathogenic Risk Prediction for Rare Nonsynonymous Single Nucleotide Variants." Each file includes the following columns: chr: chromosome pos: genomic position alRef: Reference allele alAlt: Alternative allele aaRef: Reference amino acid aaAlt: Altered amino acid clnSig: Clinical significance of the variant (pathogenic=1, benign=0)