PRP: Pathogenic Risk Prediction for Rare Nonsynonymous Single Nucleotide Variants
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下载链接：
https://zenodo.org/record/15162422
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资源简介：
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)
创建时间：
2025-04-11
