| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 3675 |
Name | ITGA3 |
Synonymous | integrin, alpha 3 (antigen CD49C, alpha 3 subunit of VLA-3 receptor);ITGA3;integrin, alpha 3 (antigen CD49C, alpha 3 subunit of VLA-3 receptor) |
Definition | CD49 antigen-like family member C|FRP-2|VLA-3 subunit alpha|antigen identified by monoclonal antibody J143|galactoprotein B3|integrin alpha-3|very late activation protein 3 receptor, alpha-3 subunit |
Position | 17q21.33 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.983C>T; p.A328V; 17:50072009-50072009 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.982G>A; p.A328T; 17:50072008-50072008 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.2574C>G; p.L858L; 17:50079249-50079249 |
breast | carcinoma | Substitution - coding silent |
c.3095A>G; p.H1032R; 17:50089159-50089159 |
breast | carcinoma | Substitution - Missense |
c.957T>C; p.D319D; 17:50071516-50071516 |
breast | carcinoma | Substitution - coding silent |
c.2442G>T; p.L814L; 17:50079117-50079117 |
breast | carcinoma | Substitution - coding silent |
c.2817C>T; p.I939I; 17:50080372-50080372 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.2327G>A; p.G776E; 17:50078853-50078853 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.496G>A; p.G166S; 17:50068137-50068137 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1794C>T; p.N598N; 17:50076445-50076445 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1483C>A; p.L495M; 17:50075472-50075472 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2263C>T; p.L755L; 17:50078250-50078250 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1026C>A; p.I342I; 17:50072052-50072052 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3068G>A; p.R1023H; 17:50089132-50089132 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.722A>G; p.D241G; 17:50070901-50070901 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3185G>A; p.R1062Q; 17:50089249-50089249 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.584G>T; p.G195V; 17:50068225-50068225 |
endometrium | carcinoma; serous_carcinoma | Substitution - Missense |
c.636C>T; p.F212F; 17:50068277-50068277 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2154C>T; p.I718I; 17:50078060-50078060 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3062G>A; p.R1021Q; 17:50089126-50089126 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1186T>G; p.L396V; 17:50073945-50073945 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.996C>T; p.F332F; 17:50072022-50072022 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1230T>C; p.L410L; 17:50073989-50073989 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.2155G>A; p.A719T; 17:50078061-50078061 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1707C>G; p.I569M; 17:50076358-50076358 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.833T>C; p.M278T; 17:50071392-50071392 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.710A>G; p.Y237C; 17:50070889-50070889 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.695G>T; p.W232L; 17:50070874-50070874 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.2118C>G; p.N706K; 17:50077426-50077426 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.2839C>T; p.R947*; 17:50081328-50081328 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2922C>A; p.F974L; 17:50087746-50087746 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.78C>T; p.G26G; 17:50056517-50056517 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.206+1G>A; p.?; 17:50056646-50056646 |
large_intestine; rectum | carcinoma; adenocarcinoma | Unknown |
c.2205G>A; p.Q735Q; 17:50078111-50078111 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2205G>A; p.Q735Q; 17:50078111-50078111 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2205G>A; p.Q735Q; 17:50078111-50078111 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.996C>T; p.F332F; 17:50072022-50072022 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2642G>C; p.G881A; 17:50079493-50079493 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3019G>T; p.G1007W; 17:50087843-50087843 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.903G>A; p.S301S; 17:50071462-50071462 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.705T>A; p.S235S; 17:50070884-50070884 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1070C>A; p.P357H; 17:50072096-50072096 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2191G>A; p.D731N; 17:50078097-50078097 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2019G>A; p.A673A; 17:50077070-50077070 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2206C>G; p.L736V; 17:50078112-50078112 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2310G>A; p.R770R; 17:50078836-50078836 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2209C>T; p.Q737*; 17:50078115-50078115 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2871C>T; p.F957F; 17:50081360-50081360 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2466C>T; p.Y822Y; 17:50079141-50079141 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1090C>T; p.P364S; 17:50072116-50072116 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2850A>T; p.V950V; 17:50081339-50081339 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.703T>C; p.S235P; 17:50070882-50070882 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.913G>A; p.A305T; 17:50071472-50071472 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1943T>C; p.V648A; 17:50076994-50076994 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2554C>G; p.L852V; 17:50079229-50079229 |
large_intestine; colon | NS | Substitution - Missense |
c.1833C>T; p.F611F; 17:50076592-50076592 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1230T>C; p.L410L; 17:50073989-50073989 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2155G>A; p.A719T; 17:50078061-50078061 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1015delG; p.G340fs*7; 17:50072041-50072041 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2332A>G; p.T778A; 17:50078858-50078858 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1982G>A; p.R661Q; 17:50077033-50077033 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.250T>C; p.Y84H; 17:50064120-50064120 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1393G>A; p.V465I; 17:50074458-50074458 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.705T>C; p.S235S; 17:50070884-50070884 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.839C>T; p.A280V; 17:50071398-50071398 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1022C>T; p.A341V; 17:50072048-50072048 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2351G>T; p.G784V; 17:50078877-50078877 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.221delC; p.R76fs*31; 17:50064091-50064091 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1765C>T; p.R589W; 17:50076416-50076416 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1252C>A; p.H418N; 17:50074150-50074150 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2074G>C; p.G692R; 17:50077382-50077382 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.467G>T; p.R156L; 17:50068108-50068108 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.686G>A; p.R229H; 17:50070865-50070865 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2560A>G; p.N854D; 17:50079235-50079235 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2839C>T; p.R947*; 17:50081328-50081328 |
liver | carcinoma | Substitution - Nonsense |
c.3185G>A; p.R1062Q; 17:50089249-50089249 |
liver | carcinoma | Substitution - Missense |
c.1645C>T; p.R549C; 17:50075706-50075706 |
liver | carcinoma | Substitution - Missense |
c.1645C>T; p.R549C; 17:50075706-50075706 |
liver | carcinoma | Substitution - Missense |
c.2297+4G>A; p.?; 17:50078288-50078288 |
liver | carcinoma | Unknown |
c.2429G>A; p.G810D; 17:50079104-50079104 |
liver | carcinoma | Substitution - Missense |
c.1583G>T; p.R528L; 17:50075644-50075644 |
liver | carcinoma | Substitution - Missense |
c.1583G>T; p.R528L; 17:50075644-50075644 |
liver | carcinoma | Substitution - Missense |
c.2086G>T; p.A696S; 17:50077394-50077394 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.513G>T; p.L171L; 17:50068154-50068154 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1466C>T; p.S489F; 17:50074531-50074531 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2876G>T; p.R959L; 17:50081365-50081365 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1842G>T; p.E614D; 17:50076601-50076601 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.582G>T; p.T194T; 17:50068223-50068223 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2136G>C; p.Q712H; 17:50077444-50077444 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1547A>G; p.Y516C; 17:50075608-50075608 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1748G>A; p.R583H; 17:50076399-50076399 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1197G>T; p.V399V; 17:50073956-50073956 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2436G>A; p.G812G; 17:50079111-50079111 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1777G>A; p.A593T; 17:50076428-50076428 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.475G>T; p.V159L; 17:50068116-50068116 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1742C>T; p.P581L; 17:50076393-50076393 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.690G>T; p.K230N; 17:50070869-50070869 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1617C>T; p.F539F; 17:50075678-50075678 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3005G>T; p.G1002V; 17:50087829-50087829 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.466C>G; p.R156G; 17:50068107-50068107 |
NS | malignant_melanoma | Substitution - Missense |
c.1100C>G; p.S367C; 17:50072126-50072126 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.639C>T; p.G213G; 17:50068280-50068280 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2615G>T; p.R872L; 17:50079466-50079466 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1207C>T; p.H403Y; 17:50073966-50073966 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1246G>A; p.V416I; 17:50074144-50074144 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1091C>G; p.P364R; 17:50072117-50072117 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.703T>C; p.S235P; 17:50070882-50070882 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1678A>C; p.N560H; 17:50076329-50076329 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.2179C>T; p.L727L; 17:50078085-50078085 |
ovary | other; neoplasm | Substitution - coding silent |
c.2179C>T; p.L727L; 17:50078085-50078085 |
ovary | other; neoplasm | Substitution - coding silent |
c.1389G>T; p.R463R; 17:50074454-50074454 |
pancreas | NS | Substitution - coding silent |
c.1583G>A; p.R528Q; 17:50075644-50075644 |
pituitary; craniopharyngeal_duct | craniopharyngioma; adamantinomatous | Substitution - Missense |
c.1202T>A; p.I401N; 17:50073961-50073961 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1787T>G; p.I596S; 17:50076438-50076438 |
prostate | carcinoma | Substitution - Missense |
c.584G>T; p.G195V; 17:50068225-50068225 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.417C>T; p.V139V; 17:50068058-50068058 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1712C>T; p.S571F; 17:50076363-50076363 |
skin | malignant_melanoma | Substitution - Missense |
c.1596C>T; p.A532A; 17:50075657-50075657 |
skin | malignant_melanoma | Substitution - coding silent |
c.2177C>T; p.T726I; 17:50078083-50078083 |
skin | malignant_melanoma | Substitution - Missense |
c.711T>C; p.Y237Y; 17:50070890-50070890 |
skin | malignant_melanoma | Substitution - coding silent |
c.340C>A; p.P114T; 17:50064533-50064533 |
skin | malignant_melanoma | Substitution - Missense |
c.2928G>A; p.V976V; 17:50087752-50087752 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2766C>T; p.P922P; 17:50080321-50080321 |
skin | malignant_melanoma | Substitution - coding silent |
c.2257A>T; p.T753S; 17:50078244-50078244 |
skin | malignant_melanoma | Substitution - Missense |
c.2836G>C; p.D946H; 17:50081325-50081325 |
skin; leg | malignant_melanoma | Substitution - Missense |
c.1341C>T; p.D447D; 17:50074239-50074239 |
skin | malignant_melanoma | Substitution - coding silent |
c.226C>T; p.R76W; 17:50064096-50064096 |
skin | malignant_melanoma | Substitution - Missense |
c.126G>A; p.V42V; 17:50056565-50056565 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1174C>T; p.P392S; 17:50073933-50073933 |
skin | malignant_melanoma | Substitution - Missense |
c.2994C>T; p.A998A; 17:50087818-50087818 |
skin | malignant_melanoma | Substitution - coding silent |
c.1091C>T; p.P364L; 17:50072117-50072117 |
skin | malignant_melanoma | Substitution - Missense |
c.2372T>A; p.V791E; 17:50078898-50078898 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2398C>T; p.Q800*; 17:50078924-50078924 |
skin | malignant_melanoma | Substitution - Nonsense |
c.175C>T; p.H59Y; 17:50056614-50056614 |
skin | malignant_melanoma | Substitution - Missense |
c.1695C>T; p.L565L; 17:50076346-50076346 |
skin | malignant_melanoma | Substitution - coding silent |
c.1463C>T; p.T488I; 17:50074528-50074528 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1469+10T>C; p.?; 17:50074544-50074544 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.2916G>A; p.T972T; 17:50081405-50081405 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2285C>T; p.T762I; 17:50078272-50078272 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.837C>T; p.G279G; 17:50071396-50071396 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.493C>T; p.R165*; 17:50068134-50068134 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2155G>A; p.A719T; 17:50078061-50078061 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.581C>T; p.T194M; 17:50068222-50068222 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2490G>A; p.L830L; 17:50079165-50079165 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2074G>A; p.G692R; 17:50077382-50077382 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2074G>A; p.G692R; 17:50077382-50077382 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2219+1G>A; p.?; 17:50078126-50078126 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.1035C>T; p.F345F; 17:50072061-50072061 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - coding silent |
c.2774C>T; p.T925I; 17:50080329-50080329 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.858G>T; p.Q286H; 17:50071417-50071417 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1382G>A; p.R461Q; 17:50074280-50074280 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1230T>C; p.L410L; 17:50073989-50073989 |
thyroid | other; neoplasm | Substitution - coding silent |
c.2621G>T; p.R874L; 17:50079472-50079472 |
thyroid | carcinoma | Substitution - Missense |
c.2368G>A; p.D790N; 17:50078894-50078894 |
thyroid | carcinoma | Substitution - Missense |
c.2055G>A; p.L685L; 17:50077106-50077106 |
thyroid | carcinoma; anaplastic_carcinoma | Substitution - coding silent |
c.2055G>A; p.L685L; 17:50077106-50077106 |
thyroid | carcinoma; anaplastic_carcinoma | Substitution - coding silent |
c.2046_2047insCTG; p.L685_S686insL; 17:50077097-50077098 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - In frame |
c.1961G>C; p.S654T; 17:50077012-50077012 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1961G>C; p.S654T; 17:50077012-50077012 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.2223G>A; p.S741S; 17:50078210-50078210 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.2534C>A; p.P845H; 17:50079209-50079209 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2140-1G>A; p.?; 17:50078045-50078045 |
urinary_tract; bladder | carcinoma | Unknown |
c.2472C>T; p.V824V; 17:50079147-50079147 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.2472C>T; p.V824V; 17:50079147-50079147 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.1066C>T; p.H356Y; 17:50072092-50072092 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.187G>A; p.E63K; 17:50056626-50056626 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1791C>T; p.L597L; 17:50076442-50076442 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |