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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%