| Tissue | Expression Dynamics | Abbreviation |
| Cervix |  | CC: Cervix cancer |
| HSIL_HPV: HPV-infected high-grade squamous intraepithelial lesions |
| N_HPV: HPV-infected normal cervix |
| Colorectum (GSE201348) |  | FAP: Familial adenomatous polyposis |
| CRC: Colorectal cancer |
| Colorectum (HTA11) |  | AD: Adenomas |
| SER: Sessile serrated lesions |
| MSI-H: Microsatellite-high colorectal cancer |
| MSS: Microsatellite stable colorectal cancer |
| Endometrium |  | AEH: Atypical endometrial hyperplasia |
| EEC: Endometrioid Cancer |
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias |
| LGIN: Low-grade intraepithelial neoplasias |
| GC |  | CAG: Chronic atrophic gastritis |
| CAG with IM: Chronic atrophic gastritis with intestinal metaplasia |
| CSG: Chronic superficial gastritis |
| GC: Gastric cancer |
| SIM: Severe intestinal metaplasia |
| WIM: Wild intestinal metaplasia |
| Liver |  | HCC: Hepatocellular carcinoma |
| NAFLD: Non-alcoholic fatty liver disease |
| Lung |  | AAH: Atypical adenomatous hyperplasia |
| AIS: Adenocarcinoma in situ |
| IAC: Invasive lung adenocarcinoma |
| MIA: Minimally invasive adenocarcinoma |
| Oral Cavity |  | EOLP: Erosive Oral lichen planus |
| LP: leukoplakia |
| NEOLP: Non-erosive oral lichen planus |
| OSCC: Oral squamous cell carcinoma |
| Prostate |  | BPH: Benign Prostatic Hyperplasia |
| Skin |  | AK: Actinic keratosis |
| cSCC: Cutaneous squamous cell carcinoma |
| SCCIS:squamous cell carcinoma in situ |
| Thyroid |  | ATC: Anaplastic thyroid cancer |
| HT: Hashimoto's thyroiditis |
| PTC: Papillary thyroid cancer |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| GO:00003983 | Colorectum | MSI-H | mRNA splicing, via spliceosome | 66/1319 | 320/18723 | 1.51e-15 | 4.41e-13 | 66 |
| GO:00434843 | Colorectum | MSI-H | regulation of RNA splicing | 34/1319 | 148/18723 | 5.85e-10 | 8.33e-08 | 34 |
| GO:00480243 | Colorectum | MSI-H | regulation of mRNA splicing, via spliceosome | 24/1319 | 101/18723 | 9.78e-08 | 9.53e-06 | 24 |
| GO:00003803 | Colorectum | MSI-H | alternative mRNA splicing, via spliceosome | 19/1319 | 77/18723 | 1.12e-06 | 7.69e-05 | 19 |
| GO:19033113 | Colorectum | MSI-H | regulation of mRNA metabolic process | 43/1319 | 288/18723 | 2.31e-06 | 1.40e-04 | 43 |
| GO:00341013 | Colorectum | MSI-H | erythrocyte homeostasis | 24/1319 | 129/18723 | 1.03e-05 | 4.79e-04 | 24 |
| GO:00300993 | Colorectum | MSI-H | myeloid cell differentiation | 50/1319 | 381/18723 | 1.52e-05 | 6.62e-04 | 50 |
| GO:00506843 | Colorectum | MSI-H | regulation of mRNA processing | 24/1319 | 137/18723 | 2.91e-05 | 1.17e-03 | 24 |
| GO:00022623 | Colorectum | MSI-H | myeloid cell homeostasis | 26/1319 | 157/18723 | 3.79e-05 | 1.43e-03 | 26 |
| GO:00003813 | Colorectum | MSI-H | regulation of alternative mRNA splicing, via spliceosome | 14/1319 | 60/18723 | 5.57e-05 | 1.92e-03 | 14 |
| GO:00302183 | Colorectum | MSI-H | erythrocyte differentiation | 20/1319 | 120/18723 | 2.62e-04 | 6.65e-03 | 20 |
| GO:00488723 | Colorectum | MSI-H | homeostasis of number of cells | 34/1319 | 272/18723 | 8.10e-04 | 1.49e-02 | 34 |
| GO:00485453 | Colorectum | MSI-H | response to steroid hormone | 40/1319 | 339/18723 | 9.37e-04 | 1.64e-02 | 40 |
| GO:19037062 | Colorectum | MSI-H | regulation of hemopoiesis | 41/1319 | 367/18723 | 2.31e-03 | 3.09e-02 | 41 |
| GO:00434013 | Colorectum | MSI-H | steroid hormone mediated signaling pathway | 19/1319 | 136/18723 | 3.19e-03 | 3.93e-02 | 19 |
| GO:00097553 | Colorectum | MSI-H | hormone-mediated signaling pathway | 24/1319 | 190/18723 | 3.88e-03 | 4.51e-02 | 24 |
| GO:19033114 | Colorectum | FAP | regulation of mRNA metabolic process | 97/2622 | 288/18723 | 1.35e-17 | 4.13e-14 | 97 |
| GO:00506844 | Colorectum | FAP | regulation of mRNA processing | 51/2622 | 137/18723 | 9.70e-12 | 4.96e-09 | 51 |
| GO:00434844 | Colorectum | FAP | regulation of RNA splicing | 53/2622 | 148/18723 | 2.16e-11 | 1.02e-08 | 53 |
| GO:00480244 | Colorectum | FAP | regulation of mRNA splicing, via spliceosome | 41/2622 | 101/18723 | 4.36e-11 | 1.78e-08 | 41 |
| Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
| RBFOX2 | SNV | Missense_Mutation | | c.964A>G | p.Ser322Gly | p.S322G | O43251 | protein_coding | tolerated_low_confidence(0.31) | benign(0.015) | TCGA-AN-A0AK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| RBFOX2 | SNV | Missense_Mutation | novel | c.383N>C | p.Asn128Thr | p.N128T | O43251 | protein_coding | tolerated(0.93) | benign(0.019) | TCGA-D8-A1XG-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
| RBFOX2 | SNV | Missense_Mutation | | c.434N>T | p.Ser145Leu | p.S145L | O43251 | protein_coding | deleterious(0.04) | benign(0.015) | TCGA-D8-A27G-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| RBFOX2 | SNV | Missense_Mutation | novel | c.383N>C | p.Asn128Thr | p.N128T | O43251 | protein_coding | tolerated(0.93) | benign(0.019) | TCGA-E9-A1RE-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | tamoxiphen | SD |
| RBFOX2 | insertion | Frame_Shift_Ins | novel | c.547_548insTTTAT | p.Arg183LeufsTer29 | p.R183Lfs*29 | O43251 | protein_coding | | | TCGA-A8-A079-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | 5-fluorouracil | SD |
| RBFOX2 | insertion | Nonsense_Mutation | novel | c.546_547insGCATTACGATGATAGGATTGCAGATTAT | p.Arg183AlafsTer4 | p.R183Afs*4 | O43251 | protein_coding | | | TCGA-A8-A079-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | 5-fluorouracil | SD |
| RBFOX2 | SNV | Missense_Mutation | | c.1073G>A | p.Arg358Gln | p.R358Q | O43251 | protein_coding | deleterious(0.02) | probably_damaging(0.996) | TCGA-C5-A1MH-01 | Cervix | cervical & endocervical cancer | Female | >=65 | III/IV | Chemotherapy | cisplatin | PD |
| RBFOX2 | SNV | Missense_Mutation | novel | c.511N>C | p.Ser171Arg | p.S171R | O43251 | protein_coding | tolerated(0.3) | benign(0.147) | TCGA-5M-AAT6-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Unknown | Unknown | PD |
| RBFOX2 | SNV | Missense_Mutation | | c.1018N>A | p.Ala340Thr | p.A340T | O43251 | protein_coding | tolerated(0.06) | benign(0.154) | TCGA-AA-3877-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| RBFOX2 | SNV | Missense_Mutation | novel | c.292N>T | p.Ile98Phe | p.I98F | O43251 | protein_coding | tolerated_low_confidence(0.09) | possibly_damaging(0.791) | TCGA-AM-5820-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |