| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 51637 |
Name | C14orf166 |
Synonymous | chromosome 14 open reading frame 166;C14orf166;chromosome 14 open reading frame 166 |
Definition | CLE7 homolog|RLL motif containing 1|UPF0568 protein C14orf166 |
Position | 14q22.1 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.101A>G; p.D34G; 14:51991356-51991356 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.101A>G; p.D34G; 14:51991356-51991356 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.177C>A; p.F59L; 14:51991432-51991432 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.301G>C; p.D101H; 14:51998508-51998508 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.521A>G; p.Q174R; 14:52001856-52001856 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.226C>T; p.R76*; 14:51993762-51993762 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.226C>T; p.R76*; 14:51993762-51993762 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.226C>T; p.R76*; 14:51993762-51993762 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.433C>T; p.R145C; 14:51999767-51999767 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.215A>G; p.K72R; 14:51993751-51993751 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.41C>T; p.P14L; 14:51989680-51989680 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.589C>A; p.L197I; 14:52004370-52004370 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.425A>G; p.Q142R; 14:51999759-51999759 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.340A>G; p.T114A; 14:51998547-51998547 |
liver | carcinoma | Substitution - Missense |
c.340A>G; p.T114A; 14:51998547-51998547 |
liver | carcinoma | Substitution - Missense |
c.398G>A; p.G133D; 14:51999732-51999732 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.162C>T; p.S54S; 14:51991417-51991417 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.426G>T; p.Q142H; 14:51999760-51999760 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.307G>T; p.V103L; 14:51998514-51998514 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.636C>G; p.L212L; 14:52004417-52004417 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.470G>A; p.R157Q; 14:52001805-52001805 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; hairy_cell_leukaemia | Substitution - Missense |
c.377A>C; p.N126T; 14:51999711-51999711 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.645A>G; p.L215L; 14:52004426-52004426 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.437A>G; p.H146R; 14:51999771-51999771 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.717G>A; p.L239L; 14:52004498-52004498 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.250C>A; p.L84I; 14:51993786-51993786 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.688A>G; p.I230V; 14:52004469-52004469 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.487C>T; p.R163C; 14:52001822-52001822 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.487C>T; p.R163C; 14:52001822-52001822 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.657C>A; p.I219I; 14:52004438-52004438 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.595G>A; p.E199K; 14:52004376-52004376 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.213C>T; p.F71F; 14:51993749-51993749 |
skin | malignant_melanoma | Substitution - coding silent |
c.562C>A; p.L188I; 14:52004224-52004224 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.562C>A; p.L188I; 14:52004224-52004224 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.314A>G; p.D105G; 14:51998521-51998521 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.84C>T; p.F28F; 14:51991339-51991339 |
skin | malignant_melanoma | Substitution - coding silent |
c.177C>T; p.F59F; 14:51991432-51991432 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |