GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:000081912 | Skin | cSCC | sister chromatid segregation | 110/4864 | 202/18723 | 5.56e-18 | 6.58e-16 | 110 |
GO:000705912 | Skin | cSCC | chromosome segregation | 161/4864 | 346/18723 | 8.34e-17 | 8.57e-15 | 161 |
GO:00482854 | Skin | cSCC | organelle fission | 197/4864 | 488/18723 | 1.51e-12 | 8.36e-11 | 197 |
GO:009881311 | Skin | cSCC | nuclear chromosome segregation | 126/4864 | 281/18723 | 4.76e-12 | 2.53e-10 | 126 |
GO:00002803 | Skin | cSCC | nuclear division | 178/4864 | 439/18723 | 1.17e-11 | 5.93e-10 | 178 |
GO:000170124 | Skin | cSCC | in utero embryonic development | 150/4864 | 367/18723 | 2.47e-10 | 1.04e-08 | 150 |
GO:00519834 | Skin | cSCC | regulation of chromosome segregation | 52/4864 | 91/18723 | 2.88e-10 | 1.20e-08 | 52 |
GO:0010639111 | Skin | cSCC | negative regulation of organelle organization | 140/4864 | 348/18723 | 3.35e-09 | 1.15e-07 | 140 |
GO:190198714 | Skin | cSCC | regulation of cell cycle phase transition | 150/4864 | 390/18723 | 3.21e-08 | 8.61e-07 | 150 |
GO:000182413 | Skin | cSCC | blastocyst development | 53/4864 | 106/18723 | 9.74e-08 | 2.32e-06 | 53 |
GO:00517832 | Skin | cSCC | regulation of nuclear division | 64/4864 | 139/18723 | 2.49e-07 | 5.25e-06 | 64 |
GO:004578613 | Skin | cSCC | negative regulation of cell cycle | 140/4864 | 385/18723 | 3.64e-06 | 5.50e-05 | 140 |
GO:00517844 | Skin | cSCC | negative regulation of nuclear division | 30/4864 | 56/18723 | 9.93e-06 | 1.30e-04 | 30 |
GO:190198812 | Skin | cSCC | negative regulation of cell cycle phase transition | 94/4864 | 249/18723 | 2.65e-05 | 3.00e-04 | 94 |
GO:001094812 | Skin | cSCC | negative regulation of cell cycle process | 108/4864 | 294/18723 | 2.75e-05 | 3.09e-04 | 108 |
GO:000007512 | Skin | cSCC | cell cycle checkpoint | 68/4864 | 169/18723 | 3.37e-05 | 3.67e-04 | 68 |
GO:00903054 | Skin | cSCC | nucleic acid phosphodiester bond hydrolysis | 97/4864 | 261/18723 | 4.08e-05 | 4.34e-04 | 97 |
GO:000706212 | Skin | cSCC | sister chromatid cohesion | 30/4864 | 62/18723 | 1.23e-04 | 1.13e-03 | 30 |
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 |
HORMAD1 | SNV | Missense_Mutation | | c.1127N>G | p.Ser376Cys | p.S376C | Q86X24 | protein_coding | deleterious(0.03) | benign(0.007) | TCGA-AC-A5XS-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | femara | SD |
HORMAD1 | SNV | Missense_Mutation | novel | c.245T>C | p.Met82Thr | p.M82T | Q86X24 | protein_coding | deleterious(0.04) | possibly_damaging(0.9) | TCGA-BH-A8FZ-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
HORMAD1 | SNV | Missense_Mutation | | c.685N>C | p.Glu229Gln | p.E229Q | Q86X24 | protein_coding | deleterious(0) | probably_damaging(0.917) | TCGA-D8-A1JA-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | PD |
HORMAD1 | SNV | Missense_Mutation | | c.313N>G | p.Pro105Ala | p.P105A | Q86X24 | protein_coding | tolerated(0.07) | possibly_damaging(0.824) | TCGA-E2-A159-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD |
HORMAD1 | SNV | Missense_Mutation | | c.1135N>C | p.Glu379Gln | p.E379Q | Q86X24 | protein_coding | tolerated(0.14) | benign(0.04) | TCGA-GM-A2D9-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD |
HORMAD1 | SNV | Missense_Mutation | novel | c.709N>A | p.Asp237Asn | p.D237N | Q86X24 | protein_coding | deleterious(0.03) | benign(0.244) | TCGA-C5-A7X5-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | carboplatin | PD |
HORMAD1 | SNV | Missense_Mutation | | c.1154N>C | p.Arg385Thr | p.R385T | Q86X24 | protein_coding | deleterious(0) | possibly_damaging(0.691) | TCGA-IR-A3LA-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
HORMAD1 | SNV | Missense_Mutation | novel | c.589G>T | p.Asp197Tyr | p.D197Y | Q86X24 | protein_coding | deleterious(0) | possibly_damaging(0.877) | TCGA-JW-AAVH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
HORMAD1 | SNV | Missense_Mutation | rs200394759 | c.253N>C | p.Cys85Arg | p.C85R | Q86X24 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-ZJ-AAXA-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
HORMAD1 | SNV | Missense_Mutation | rs774953907 | c.1072C>T | p.Arg358Trp | p.R358W | Q86X24 | protein_coding | deleterious(0.01) | possibly_damaging(0.798) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |