| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 6489 | ||
Name | ST8SIA1 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.987C>T; p.L329L; 12:22201636-22201636 |
pancreas | carcinoma | Substitution - coding silent |
c.45C>A; p.A15A; 12:22334188-22334188 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.987C>T; p.L329L; 12:22201636-22201636 |
pancreas | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.1045G>C; p.D349H; 12:22201578-22201578 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.287A>T; p.K96I; 12:22287243-22287243 |
breast | carcinoma | Substitution - Missense |
c.853G>C; p.G285R; 12:22201770-22201770 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.66G>C; p.K22N; 12:22334167-22334167 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.590A>G; p.Q197R; 12:22202033-22202033 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.971T>C; p.M324T; 12:22201652-22201652 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.770G>A; p.R257H; 12:22201853-22201853 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.701G>A; p.R234K; 12:22201922-22201922 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.573A>T; p.I191I; 12:22249017-22249017 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.498T>G; p.N166K; 12:22249092-22249092 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.498T>G; p.N166K; 12:22249092-22249092 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.305G>A; p.G102E; 12:22287225-22287225 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.498T>G; p.N166K; 12:22249092-22249092 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.305G>A; p.G102E; 12:22287225-22287225 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.459C>T; p.G153G; 12:22255312-22255312 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.246G>T; p.M82I; 12:22287284-22287284 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.389C>G; p.P130R; 12:22255382-22255382 |
liver | carcinoma | Substitution - Missense |
c.199delG; p.A67fs*28; 12:22334034-22334034 |
liver | carcinoma | Deletion - Frameshift |
c.338A>G; p.Y113C; 12:22287192-22287192 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1036C>T; p.P346S; 12:22201587-22201587 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.975C>T; p.P325P; 12:22201648-22201648 |
skin; leg | malignant_melanoma; nodular | Substitution - coding silent |
c.219C>T; p.T73T; 12:22334014-22334014 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.60G>A; p.A20A; 12:22334173-22334173 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.60G>A; p.A20A; 12:22334173-22334173 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.99T>C; p.S33S; 12:22334134-22334134 |
thyroid | carcinoma | Substitution - coding silent |
c.314T>C; p.M105T; 12:22287216-22287216 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.860G>T; p.C287F; 12:22201763-22201763 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.148C>T; p.R50W; 12:22334085-22334085 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.854G>A; p.G285D; 12:22201769-22201769 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.415G>A; p.A139T; 12:22255356-22255356 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.244A>G; p.M82V; 12:22287286-22287286 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.815G>T; p.R272L; 12:22201808-22201808 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.48G>T; p.M16I; 12:22334185-22334185 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.102C>A; p.A34A; 12:22334131-22334131 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.501C>T; p.L167L; 12:22249089-22249089 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.201G>A; p.A67A; 12:22334032-22334032 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.699G>A; p.L233L; 12:22201924-22201924 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.589C>G; p.Q197E; 12:22202034-22202034 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.815G>A; p.R272H; 12:22201808-22201808 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.815G>A; p.R272H; 12:22201808-22201808 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.359C>T; p.S120L; 12:22287171-22287171 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.324C>T; p.D108D; 12:22287206-22287206 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.259G>A; p.D87N; 12:22287271-22287271 |
liver | carcinoma | Substitution - Missense |
c.608G>C; p.R203T; 12:22202015-22202015 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.798A>T; p.R266S; 12:22201825-22201825 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.492-1G>T; p.?; 12:22249099-22249099 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Unknown |
c.298C>T; p.P100S; 12:22287232-22287232 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.209G>A; p.R70K; 12:22334024-22334024 |
skin | malignant_melanoma | Substitution - Missense |
c.65A>G; p.K22R; 12:22334168-22334168 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.65A>G; p.K22R; 12:22334168-22334168 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.181delG; p.V61fs*34; 12:22334052-22334052 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1022G>C; p.R341T; 12:22201601-22201601 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.411A>T; p.K137N; 12:22255360-22255360 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.491G>C; p.R164P; 12:22255280-22255280 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.585-10delT; p.?; 12:22202048-22202048 |
liver | carcinoma | Unknown |
c.979G>T; p.E327*; 12:22201644-22201644 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.979G>T; p.E327*; 12:22201644-22201644 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.865G>T; p.E289*; 12:22201758-22201758 |
prostate | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.16C>A; p.R6R; 12:22334217-22334217 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.894C>T; p.F298F; 12:22201729-22201729 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.987C>A; p.L329L; 12:22201636-22201636 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.577C>T; p.R193W; 12:22249013-22249013 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.577C>T; p.R193W; 12:22249013-22249013 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.577C>T; p.R193W; 12:22249013-22249013 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.577C>T; p.R193W; 12:22249013-22249013 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.38G>T; p.R13I; 12:22334195-22334195 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1011C>T; p.I337I; 12:22201612-22201612 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1011C>T; p.I337I; 12:22201612-22201612 |
skin | malignant_melanoma | Substitution - coding silent |
c.1011C>T; p.I337I; 12:22201612-22201612 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.769C>T; p.R257C; 12:22201854-22201854 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.453C>T; p.G151G; 12:22255318-22255318 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.594C>T; p.N198N; 12:22202029-22202029 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.465A>T; p.Q155H; 12:22255306-22255306 |
pancreas | carcinoma | Substitution - Missense |
c.444G>T; p.K148N; 12:22255327-22255327 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.465A>T; p.Q155H; 12:22255306-22255306 |
pancreas | carcinoma; ductal_carcinoma | Substitution - Missense |
c.465A>T; p.Q155H; 12:22255306-22255306 |
pancreas | pancreatic_intraepithelial_neoplasia_(PanIN) | Substitution - Missense |
c.819G>C; p.L273L; 12:22201804-22201804 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.585-10_585-9insT; p.?; 12:22202047-22202048 |
skin | malignant_melanoma | Unknown |
c.585-10_585-9insT; p.?; 12:22202047-22202048 |
NS | malignant_melanoma | Unknown |
c.809C>A; p.A270D; 12:22201814-22201814 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.413_414GC>TT; p.C138F; 12:22255357-22255358 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.417G>A; p.A139A; 12:22255354-22255354 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.243A>C; p.Q81H; 12:22287287-22287287 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.774C>T; p.S258S; 12:22201849-22201849 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.492-10G>T; p.?; 12:22249108-22249108 |
pancreas | carcinoma | Unknown |
c.736C>G; p.Q246E; 12:22201887-22201887 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.996G>A; p.W332*; 12:22201627-22201627 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Nonsense |
c.158A>G; p.N53S; 12:22334075-22334075 |
thyroid | carcinoma | Substitution - Missense |
c.17G>A; p.R6Q; 12:22334216-22334216 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.407A>C; p.K136T; 12:22255364-22255364 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |