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. 2017 Sep 25;6(9):e380. doi: 10.1038/oncsis.2017.79

Table 2. Top 20 ReactomeDB pathways identified in differential analysis of disease-associated data sets compared with the set of common variants.

Germline cancer-associated mutations Somatic cancer-associated mutations Mutations associated with non-cancer diseases
Regulation of TP53 activity through phosphorylation PIP3 activates AKT signaling Neutrophil degranulation
Ub-specific processing proteases Oxidative stress-induced senescence Intrinsic pathway of fibrin clot formation
TP53 regulates transcription of DNA repair genes Factors involved in megakaryocyte development and platelet production Glycosphingolipid metabolism
G2/M DNA damage checkpoint Oncogene-induced senescence Gap junction assembly
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Ub-specific processing proteases Urea cycle
Factors involved in megakaryocyte development and platelet production Ovarian tumor domain proteases Platelet degranulation
PIP3 activates AKT signaling Regulation of TP53 degradation Oligomerization of connexins into connexons
Stabilization of p53 Regulation of TP53 activity through Phosphorylation Transport of connexins along the secretory pathway
Regulation of TP53 activity through methylation Pre-NOTCH transcription and translation Galactose catabolism
Regulation of TP53 degradation Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus
Formation of senescence-associated heterochromatin foci (SAHF) Association of TriC/CCT with target proteins during biosynthesis Removal of aminoterminal propeptides from gamma-carboxylated proteins
Oncogene induced senescence TP53 regulates transcription of DNA repair Genes Gamma-carboxylation of protein precursors
Oxidative stress-induced senescence G2/M DNA damage checkpoint Extrinsic pathway of fibrin clot formation
DNA damage/telomere stress-induced Senescence TP53 regulates metabolic genes Common pathway of fibrin clot formation
SUMOylation of transcription factors Regulation of TP53 activity through methylation Striated muscle contraction
Activation of NOXA and translocation to mitochondria Regulation of TP53 activity through acetylation RAF/MAP kinase cascade
Regulation of TP53 activity through acetylation TP53 regulates transcription of genes involved in Cytochrome C release Regulation of gene expression in beta cells
Transcriptional activation of cell cycle inhibitor p21 Stabilization of p53 Phenylalanine and tyrosine catabolism
PI5P regulates TP53 acetylation Regulation of TP53 activity through association with co-factors Signaling by BRAF and RAF fusions
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain DNA damage/telomere stress-induced senescence Signaling by RAS mutants

Differences of the combined scores (see Materials and methods) for disease-associated nsSNVs and common variants are shown in parentheses.