Table 1 Mutation frequency of genes with single nucleotide variations in two groups
From: Integrated genomic analysis identifies clinically relevant subtypes of renal clear cell carcinoma
Genes | EC1 | EC2–3 | P values | All |
|---|---|---|---|---|
VHL | 42.57% | 54.41% | 0.0480 | 51.70% |
PBRM1 | 25.74% | 35.35% | 0.0948 | 33.10% |
MUC4 | 20.79% | 18.25% | 0.3941 | 18.82% |
BAP1 | 19.80% | 5.89% | 4.508e-05 | 9.07% |
SETD2 | 13.86% | 12.93% | 0.9421 | 13.15% |