| Tissue | Expression Dynamics | Abbreviation |
| Breast |  | IDC: Invasive ductal carcinoma |
| DCIS: Ductal carcinoma in situ |
| Precancer(BRCA1-mut): Precancerous lesion from BRCA1 mutation carriers |
| 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 |
| Liver |  | HCC: Hepatocellular carcinoma |
| NAFLD: Non-alcoholic fatty liver disease |
| 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 |
| 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 |
| ILF2 | SNV | Missense_Mutation | | c.1170G>T | p.Glu390Asp | p.E390D | Q12905 | protein_coding | tolerated_low_confidence(0.06) | benign(0) | TCGA-BH-A18G-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| ILF2 | SNV | Missense_Mutation | | c.910C>A | p.Leu304Ile | p.L304I | Q12905 | protein_coding | deleterious(0.02) | possibly_damaging(0.871) | TCGA-BH-A1F5-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| ILF2 | SNV | Missense_Mutation | | c.890N>C | p.Arg297Thr | p.R297T | Q12905 | protein_coding | deleterious(0.01) | probably_damaging(0.987) | TCGA-C8-A12V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| ILF2 | SNV | Missense_Mutation | rs767092802 | c.725C>T | p.Pro242Leu | p.P242L | Q12905 | protein_coding | deleterious(0.03) | possibly_damaging(0.543) | TCGA-D8-A1Y3-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicine+cyclophosphamide | SD |
| ILF2 | SNV | Missense_Mutation | novel | c.119C>T | p.Ala40Val | p.A40V | Q12905 | protein_coding | tolerated(0.3) | benign(0.076) | TCGA-EW-A6SA-01 | Breast | breast invasive carcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
| ILF2 | SNV | Missense_Mutation | novel | c.937N>G | p.Thr313Ala | p.T313A | Q12905 | protein_coding | deleterious(0.04) | possibly_damaging(0.863) | TCGA-PL-A8LX-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
| ILF2 | SNV | Missense_Mutation | novel | c.644C>T | p.Ala215Val | p.A215V | Q12905 | protein_coding | deleterious(0.04) | possibly_damaging(0.777) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| ILF2 | SNV | Missense_Mutation | rs768322800 | c.481N>A | p.Glu161Lys | p.E161K | Q12905 | protein_coding | tolerated(0.09) | benign(0.392) | TCGA-EK-A3GK-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
| ILF2 | SNV | Missense_Mutation | | c.493G>A | p.Glu165Lys | p.E165K | Q12905 | protein_coding | tolerated(0.11) | benign(0.211) | TCGA-AY-6196-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | SD |
| ILF2 | SNV | Missense_Mutation | | c.1155N>A | p.Ser385Arg | p.S385R | Q12905 | protein_coding | deleterious_low_confidence(0.03) | benign(0.207) | TCGA-CM-4744-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |