Additional file 3: Table S1. of Application of single-cell RNA sequencing in optimizing a combinatorial therapeutic strategy in metastatic renal cell carcinoma

Somatic mutations identified in tumor samples from whole-exome sequencing. Single-nucleotide variants (SNVs) were annotated by implementing SnpEff. Whole-exome sequencing data of paired patient blood was used to identify somatic variants in parental tumors and matched xenografts of pRCCs and mRCCs, which are shown in separate sheets. (XLSX 218 kb)