GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:001605525 | Thyroid | ATC | Wnt signaling pathway | 234/6293 | 444/18723 | 4.64e-17 | 4.31e-15 | 234 |
GO:019873825 | Thyroid | ATC | cell-cell signaling by wnt | 234/6293 | 446/18723 | 9.26e-17 | 8.25e-15 | 234 |
GO:003011125 | Thyroid | ATC | regulation of Wnt signaling pathway | 177/6293 | 328/18723 | 1.83e-14 | 1.05e-12 | 177 |
GO:001604927 | Thyroid | ATC | cell growth | 241/6293 | 482/18723 | 4.27e-14 | 2.35e-12 | 241 |
GO:006082825 | Thyroid | ATC | regulation of canonical Wnt signaling pathway | 134/6293 | 253/18723 | 1.49e-10 | 4.56e-09 | 134 |
GO:000155826 | Thyroid | ATC | regulation of cell growth | 201/6293 | 414/18723 | 1.57e-10 | 4.76e-09 | 201 |
GO:006007025 | Thyroid | ATC | canonical Wnt signaling pathway | 154/6293 | 303/18723 | 3.68e-10 | 1.02e-08 | 154 |
GO:000183722 | Thyroid | ATC | epithelial to mesenchymal transition | 87/6293 | 157/18723 | 1.50e-08 | 3.06e-07 | 87 |
GO:004876221 | Thyroid | ATC | mesenchymal cell differentiation | 116/6293 | 236/18723 | 5.08e-07 | 7.30e-06 | 116 |
GO:006048521 | Thyroid | ATC | mesenchyme development | 136/6293 | 291/18723 | 2.04e-06 | 2.43e-05 | 136 |
GO:003017815 | Thyroid | ATC | negative regulation of Wnt signaling pathway | 85/6293 | 170/18723 | 6.94e-06 | 7.16e-05 | 85 |
GO:004592622 | Thyroid | ATC | negative regulation of growth | 115/6293 | 249/18723 | 2.34e-05 | 2.06e-04 | 115 |
GO:003030813 | Thyroid | ATC | negative regulation of cell growth | 90/6293 | 188/18723 | 3.35e-05 | 2.78e-04 | 90 |
GO:001071712 | Thyroid | ATC | regulation of epithelial to mesenchymal transition | 53/6293 | 99/18723 | 3.42e-05 | 2.82e-04 | 53 |
GO:009009014 | Thyroid | ATC | negative regulation of canonical Wnt signaling pathway | 66/6293 | 137/18723 | 2.82e-04 | 1.80e-03 | 66 |
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 |
DACT3 | SNV | Missense_Mutation | | c.1861N>T | p.Gly621Cys | p.G621C | Q96B18 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-A8-A09E-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | anastrozole | SD |
DACT3 | insertion | Frame_Shift_Ins | novel | c.1620_1621insAAGCGGCCCTCAGCCGGGCT | p.Val541LysfsTer70 | p.V541Kfs*70 | Q96B18 | protein_coding | | | TCGA-A8-A081-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
DACT3 | insertion | In_Frame_Ins | novel | c.1774_1775insAACCAC | p.Ala592delinsGluProPro | p.A592delinsEPP | Q96B18 | protein_coding | | | TCGA-A8-A08J-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | PD |
DACT3 | insertion | Frame_Shift_Ins | novel | c.1772_1773insCG | p.Ala592ValfsTer13 | p.A592Vfs*13 | Q96B18 | protein_coding | | | TCGA-A8-A08J-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | PD |
DACT3 | insertion | Frame_Shift_Ins | novel | c.1620_1621insTCAGCCGGGCT | p.Val541SerfsTer67 | p.V541Sfs*67 | Q96B18 | protein_coding | | | TCGA-BH-A0AW-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | SD |
DACT3 | SNV | Missense_Mutation | novel | c.374N>A | p.Gly125Glu | p.G125E | Q96B18 | protein_coding | tolerated(0.09) | benign(0.139) | TCGA-VS-A8EK-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | PD |
DACT3 | SNV | Missense_Mutation | | c.1751N>T | p.Ala584Val | p.A584V | Q96B18 | protein_coding | tolerated(0.18) | benign(0.401) | TCGA-AA-3492-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
DACT3 | SNV | Missense_Mutation | novel | c.358G>T | p.Asp120Tyr | p.D120Y | Q96B18 | protein_coding | tolerated(0.09) | probably_damaging(0.937) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR |
DACT3 | SNV | Missense_Mutation | | c.1553N>T | p.Ala518Val | p.A518V | Q96B18 | protein_coding | tolerated(0.56) | possibly_damaging(0.566) | TCGA-AY-A69D-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
DACT3 | SNV | Missense_Mutation | | c.1649C>T | p.Ser550Leu | p.S550L | Q96B18 | protein_coding | deleterious(0) | probably_damaging(0.992) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |