Additional file 2 of Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows
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Additional file 2: Table S2. List of unspecified genetic variants in the NCCN guidelines that were experimentally validated, curated by gene-specific database, or predicted as deleterious by two somatic variant predictors (intOgen & CScape).
创建时间：
2022-04-26
