| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 7436 |
Name | VLDLR |
Synonymous | very low density lipoprotein receptor;VLDLR;very low density lipoprotein receptor |
Definition | VLDL receptor|VLDL-R|very low-density lipoprotein receptor |
Position | 9p24 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1691A>G; p.D564G; 9:2646540-2646540 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.2523T>C; p.T841T; 9:2652886-2652886 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.921C>T; p.S307S; 9:2643728-2643728 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2075T>C; p.I692T; 9:2648781-2648781 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1643A>C; p.K548T; 9:2646492-2646492 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.472G>A; p.E158K; 9:2643183-2643183 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.626G>A; p.S209N; 9:2643337-2643337 |
skin; scalp | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.876T>C; p.H292H; 9:2643683-2643683 |
bone; pelvis | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.2067A>G; p.Q689Q; 9:2648773-2648773 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.1171A>G; p.R391G; 9:2644838-2644838 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1401G>T; p.Q467H; 9:2645662-2645662 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1422C>A; p.L474L; 9:2645683-2645683 |
thyroid | other; neoplasm | Substitution - coding silent |
c.402T>C; p.C134C; 9:2641453-2641453 |
skin | malignant_melanoma | Substitution - coding silent |
c.109C>A; p.Q37K; 9:2635479-2635479 |
liver | carcinoma | Substitution - Missense |
c.109C>A; p.Q37K; 9:2635479-2635479 |
liver | carcinoma | Substitution - Missense |
c.739G>A; p.G247S; 9:2643450-2643450 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1718C>T; p.S573L; 9:2647488-2647488 |
liver | carcinoma | Substitution - Missense |
c.1718C>T; p.S573L; 9:2647488-2647488 |
liver | carcinoma | Substitution - Missense |
c.648A>G; p.A216A; 9:2643359-2643359 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.1917G>A; p.K639K; 9:2648302-2648302 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.836G>A; p.R279Q; 9:2643643-2643643 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.141G>A; p.T47T; 9:2635511-2635511 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1061_1066+23del29; p.?; 9:2643954-2643982 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Unknown |
c.364G>A; p.A122T; 9:2641415-2641415 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.364G>A; p.A122T; 9:2641415-2641415 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.364G>A; p.A122T; 9:2641415-2641415 |
liver | carcinoma | Substitution - Missense |
c.2068G>T; p.D690Y; 9:2648774-2648774 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1066+1G>A; p.?; 9:2643960-2643960 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.1667G>A; p.R556Q; 9:2646516-2646516 |
breast | carcinoma | Substitution - Missense |
c.1838G>A; p.R613H; 9:2648223-2648223 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.910G>T; p.V304F; 9:2643717-2643717 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.2032C>T; p.L678L; 9:2648738-2648738 |
pancreas | carcinoma | Substitution - coding silent |
c.561C>G; p.D187E; 9:2643272-2643272 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.232G>A; p.V78M; 9:2639888-2639888 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.232G>A; p.V78M; 9:2639888-2639888 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.834C>T; p.C278C; 9:2643641-2643641 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.1052C>T; p.P351L; 9:2643945-2643945 |
skin | malignant_melanoma | Substitution - Missense |
c.195G>T; p.K65N; 9:2635565-2635565 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.827G>A; p.R276Q; 9:2643634-2643634 |
breast | carcinoma | Substitution - Missense |
c.1963-1G>T; p.?; 9:2648668-2648668 |
endometrium | carcinoma; endometrioid_carcinoma | Unknown |
c.827G>A; p.R276Q; 9:2643634-2643634 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1343G>A; p.R448Q; 9:2645604-2645604 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1343G>A; p.R448Q; 9:2645604-2645604 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1343G>A; p.R448Q; 9:2645604-2645604 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1798C>T; p.Q600*; 9:2647568-2647568 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1676C>T; p.A559V; 9:2646525-2646525 |
large_intestine; colon | NS | Substitution - Missense |
c.161G>A; p.G54E; 9:2635531-2635531 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.835C>T; p.R279*; 9:2643642-2643642 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - Nonsense |
c.567C>T; p.A189A; 9:2643278-2643278 |
liver | carcinoma | Substitution - coding silent |
c.567C>T; p.A189A; 9:2643278-2643278 |
liver | carcinoma | Substitution - coding silent |
c.1900C>T; p.R634C; 9:2648285-2648285 |
skin | malignant_melanoma | Substitution - Missense |
c.1790C>T; p.A597V; 9:2647560-2647560 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1767C>T; p.F589F; 9:2647537-2647537 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.231C>T; p.F77F; 9:2639887-2639887 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.231C>T; p.F77F; 9:2639887-2639887 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.231C>T; p.F77F; 9:2639887-2639887 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2463T>C; p.N821N; 9:2652826-2652826 |
bone; pelvis | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.2463T>A; p.N821K; 9:2652826-2652826 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1200C>T; p.C400C; 9:2644970-2644970 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2395G>A; p.A799T; 9:2651933-2651933 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2395G>A; p.A799T; 9:2651933-2651933 |
pancreas | NS | Substitution - Missense |
c.2179G>A; p.D727N; 9:2650444-2650444 |
breast | carcinoma | Substitution - Missense |
c.922G>A; p.D308N; 9:2643729-2643729 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1090A>C; p.N364H; 9:2644757-2644757 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.922G>A; p.D308N; 9:2643729-2643729 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2416+8G>T; p.?; 9:2651962-2651962 |
liver | carcinoma; hepatocellular_carcinoma | Unknown |
c.1168G>T; p.D390Y; 9:2644835-2644835 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.738C>T; p.C246C; 9:2643449-2643449 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.188A>G; p.D63G; 9:2635558-2635558 |
thyroid | carcinoma | Substitution - Missense |
c.2586+2T>C; p.?; 9:2652951-2652951 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.2576C>T; p.T859M; 9:2652939-2652939 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.493C>T; p.R165C; 9:2643204-2643204 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2384G>A; p.G795E; 9:2651922-2651922 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.275A>T; p.D92V; 9:2639931-2639931 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.2307T>G; p.I769M; 9:2651470-2651470 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.692G>A; p.R231H; 9:2643403-2643403 |
breast | carcinoma | Substitution - Missense |
c.692G>A; p.R231H; 9:2643403-2643403 |
breast | carcinoma | Substitution - Missense |
c.1809C>A; p.N603K; 9:2647579-2647579 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.674C>G; p.S225C; 9:2643385-2643385 |
liver | carcinoma | Substitution - Missense |
c.1656C>T; p.N552N; 9:2646505-2646505 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - coding silent |
c.674C>G; p.S225C; 9:2643385-2643385 |
liver | carcinoma | Substitution - Missense |
c.149G>T; p.W50L; 9:2635519-2635519 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1505T>C; p.V502A; 9:2646354-2646354 |
skin | malignant_melanoma | Substitution - Missense |
c.434A>C; p.D145A; 9:2641485-2641485 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.2557A>G; p.S853G; 9:2652920-2652920 |
breast | carcinoma | Substitution - Missense |
c.2422T>C; p.L808L; 9:2652785-2652785 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2394C>T; p.A798A; 9:2651932-2651932 |
prostate | carcinoma | Substitution - coding silent |
c.1117G>T; p.D373Y; 9:2644784-2644784 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2388T>G; p.T796T; 9:2651926-2651926 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.422A>G; p.D141G; 9:2641473-2641473 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.936C>A; p.C312*; 9:2643743-2643743 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1892G>A; p.G631D; 9:2648277-2648277 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.294A>G; p.E98E; 9:2639950-2639950 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1353C>T; p.I451I; 9:2645614-2645614 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1871T>C; p.L624S; 9:2648256-2648256 |
liver | carcinoma | Substitution - Missense |
c.1685C>A; p.A562D; 9:2646534-2646534 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1589C>T; p.T530I; 9:2646438-2646438 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1427C>T; p.A476V; 9:2645688-2645688 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2302G>T; p.E768*; 9:2651465-2651465 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2309C>T; p.S770L; 9:2651472-2651472 |
skin | malignant_melanoma | Substitution - Missense |
c.898A>G; p.I300V; 9:2643705-2643705 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1679C>T; p.S560F; 9:2646528-2646528 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1378G>T; p.E460*; 9:2645639-2645639 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2434G>A; p.A812T; 9:2652797-2652797 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2459G>A; p.R820Q; 9:2652822-2652822 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.211A>G; p.T71A; 9:2639867-2639867 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.434A>G; p.D145G; 9:2641485-2641485 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1755A>G; p.G585G; 9:2647525-2647525 |
skin | malignant_melanoma | Substitution - coding silent |
c.1208C>T; p.P403L; 9:2644978-2644978 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.130C>T; p.R44C; 9:2635500-2635500 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1620T>C; p.A540A; 9:2646469-2646469 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1810G>A; p.G604R; 9:2647580-2647580 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1810G>A; p.G604R; 9:2647580-2647580 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2582C>G; p.P861R; 9:2652945-2652945 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1666C>T; p.R556*; 9:2646515-2646515 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.435T>C; p.D145D; 9:2641486-2641486 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.367C>T; p.H123Y; 9:2641418-2641418 |
central_nervous_system; cerebellum | primitive_neuroectodermal_tumour-medulloblastoma; SHH_subtype | Substitution - Missense |
c.367C>T; p.H123Y; 9:2641418-2641418 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma; medullomyoblastoma | Substitution - Missense |
c.1097G>A; p.G366E; 9:2644764-2644764 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1581C>T; p.I527I; 9:2646430-2646430 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2546T>C; p.I849T; 9:2652909-2652909 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1948C>A; p.L650I; 9:2648333-2648333 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2154A>G; p.L718L; 9:2650419-2650419 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1988A>G; p.E663G; 9:2648694-2648694 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.222A>T; p.E74D; 9:2639878-2639878 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.2564C>G; p.S855C; 9:2652927-2652927 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1878C>T; p.S626S; 9:2648263-2648263 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1187-3C>T; p.?; 9:2644954-2644954 |
liver | carcinoma; hepatocellular_carcinoma | Unknown |
c.315A>G; p.P105P; 9:2639971-2639971 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1448T>C; p.L483P; 9:2645709-2645709 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.583G>A; p.A195T; 9:2643294-2643294 |
breast | carcinoma | Substitution - Missense |
c.135T>C; p.C45C; 9:2635505-2635505 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.468C>T; p.P156P; 9:2643179-2643179 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1289C>T; p.A430V; 9:2645059-2645059 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1069A>C; p.I357L; 9:2644736-2644736 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.691C>T; p.R231C; 9:2643402-2643402 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.2606delA; p.D869fs*4; 9:2653852-2653852 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Deletion - Frameshift |
c.1869G>A; p.M623I; 9:2648254-2648254 |
breast | carcinoma | Substitution - Missense |
c.386C>A; p.P129Q; 9:2641437-2641437 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |