| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 3433 |
Name | IFIT2 |
Synonymous | interferon-induced protein with tetratricopeptide repeats 2;IFIT2;interferon-induced protein with tetratricopeptide repeats 2 |
Definition | Interferon, alpha-inducible protein (MW 54kD)|interferon-induced 54 kDa protein|interferon-induced protein 54 |
Position | 10q23.31 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.410A>G; p.E137G; 10:89306366-89306366 |
skin | malignant_melanoma | Substitution - Missense |
c.755G>T; p.S252I; 10:89306711-89306711 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.292G>A; p.G98R; 10:89306248-89306248 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.621C>T; p.D207D; 10:89306577-89306577 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1075A>G; p.K359E; 10:89307031-89307031 |
liver | carcinoma | Substitution - Missense |
c.751C>T; p.R251C; 10:89306707-89306707 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1075A>G; p.K359E; 10:89307031-89307031 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.751C>T; p.R251C; 10:89306707-89306707 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1253T>A; p.I418N; 10:89307209-89307209 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.197delA; p.N67fs*14; 10:89306153-89306153 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.752G>A; p.R251H; 10:89306708-89306708 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.752G>A; p.R251H; 10:89306708-89306708 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.44A>C; p.Q15P; 10:89306000-89306000 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.199A>C; p.N67H; 10:89306155-89306155 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.586G>A; p.D196N; 10:89306542-89306542 |
breast | carcinoma | Substitution - Missense |
c.18G>T; p.K6N; 10:89305974-89305974 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1190A>C; p.E397A; 10:89307146-89307146 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1141C>T; p.Q381*; 10:89307097-89307097 |
urinary_tract; bladder | carcinoma | Substitution - Nonsense |
c.658C>T; p.H220Y; 10:89306614-89306614 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1141C>A; p.Q381K; 10:89307097-89307097 |
breast | carcinoma | Substitution - Missense |
c.363A>G; p.K121K; 10:89306319-89306319 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.637G>A; p.V213I; 10:89306593-89306593 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.470C>T; p.A157V; 10:89306426-89306426 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.470C>T; p.A157V; 10:89306426-89306426 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.470C>T; p.A157V; 10:89306426-89306426 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1057G>T; p.A353S; 10:89307013-89307013 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.929G>T; p.R310I; 10:89306885-89306885 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.886T>A; p.F296I; 10:89306842-89306842 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1126C>T; p.R376W; 10:89307082-89307082 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1186A>G; p.I396V; 10:89307142-89307142 |
liver | carcinoma | Substitution - Missense |
c.1186A>G; p.I396V; 10:89307142-89307142 |
liver | carcinoma | Substitution - Missense |
c.979G>A; p.D327N; 10:89306935-89306935 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.483T>A; p.F161L; 10:89306439-89306439 |
skin | malignant_melanoma | Substitution - Missense |
c.406_407CC>TT; p.P136L; 10:89306362-89306363 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.360G>A; p.V120V; 10:89306316-89306316 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.360G>A; p.V120V; 10:89306316-89306316 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.625C>A; p.Q209K; 10:89306581-89306581 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.389C>T; p.P130L; 10:89306345-89306345 |
skin; shoulder | malignant_melanoma | Substitution - Missense |
c.1264C>T; p.R422*; 10:89307220-89307220 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.797C>T; p.A266V; 10:89306753-89306753 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.218G>T; p.C73F; 10:89306174-89306174 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.701A>G; p.K234R; 10:89306657-89306657 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.551G>A; p.R184H; 10:89306507-89306507 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.362A>G; p.K121R; 10:89306318-89306318 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.510G>T; p.K170N; 10:89306466-89306466 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.510G>T; p.K170N; 10:89306466-89306466 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.990T>C; p.N330N; 10:89306946-89306946 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.697G>T; p.E233*; 10:89306653-89306653 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.462T>A; p.N154K; 10:89306418-89306418 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.3G>T; p.M1I; 10:89302126-89302126 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3G>A; p.M1I; 10:89302126-89302126 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1217G>T; p.R406M; 10:89307173-89307173 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.594G>A; p.L198L; 10:89306550-89306550 |
breast | carcinoma | Substitution - coding silent |
c.811delA; p.K272fs*3; 10:89306767-89306767 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.733G>C; p.G245R; 10:89306689-89306689 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.66G>A; p.W22*; 10:89306022-89306022 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.161G>T; p.C54F; 10:89306117-89306117 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.906A>G; p.R302R; 10:89306862-89306862 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.906A>G; p.R302R; 10:89306862-89306862 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.394A>G; p.R132G; 10:89306350-89306350 |
skin | malignant_melanoma | Substitution - Missense |
c.5+1G>A; p.?; 10:89302129-89302129 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Unknown |
c.5+1G>A; p.?; 10:89302129-89302129 |
upper_aerodigestive_tract; mouth | carcinoma | Unknown |
c.824A>G; p.E275G; 10:89306780-89306780 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1182C>A; p.H394Q; 10:89307138-89307138 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.955G>T; p.A319S; 10:89306911-89306911 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.840T>C; p.N280N; 10:89306796-89306796 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1033G>A; p.A345T; 10:89306989-89306989 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1208A>T; p.Q403L; 10:89307164-89307164 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.121C>T; p.R41W; 10:89306077-89306077 |
skin | malignant_melanoma | Substitution - Missense |
c.592C>G; p.L198V; 10:89306548-89306548 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1246_1247insA; p.I418fs*8; 10:89307202-89307203 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.545G>T; p.S182I; 10:89306501-89306501 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.590C>T; p.P197L; 10:89306546-89306546 |
skin | malignant_melanoma | Substitution - Missense |
c.337G>A; p.V113I; 10:89306293-89306293 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.716C>T; p.A239V; 10:89306672-89306672 |
skin | malignant_melanoma | Substitution - Missense |
c.716C>T; p.A239V; 10:89306672-89306672 |
skin | malignant_melanoma | Substitution - Missense |
c.1280G>T; p.G427V; 10:89307236-89307236 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.139C>T; p.R47C; 10:89306095-89306095 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.822A>C; p.L274F; 10:89306778-89306778 |
skin | malignant_melanoma | Substitution - Missense |
c.811A>T; p.K271*; 10:89306767-89306767 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.337G>T; p.V113F; 10:89306293-89306293 |
liver | carcinoma | Substitution - Missense |
c.281T>C; p.L94P; 10:89306237-89306237 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1004G>A; p.R335H; 10:89306960-89306960 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |