| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 2886 |
Name | GRB7 |
Synonymous | growth factor receptor-bound protein 7;GRB7;growth factor receptor-bound protein 7 |
Definition | B47|GRB7 adapter protein|epidermal growth factor receptor GRB-7 |
Position | 17q12 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.253delG; p.G86fs*18; 17:39742663-39742663 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.939G>C; p.K313N; 17:39744912-39744912 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.272G>A; p.R91K; 17:39742682-39742682 |
skin | malignant_melanoma | Substitution - Missense |
c.92C>T; p.P31L; 17:39742393-39742393 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1570C>T; p.R524C; 17:39746868-39746868 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.688C>T; p.P230S; 17:39744094-39744094 |
skin | malignant_melanoma | Substitution - Missense |
c.385G>C; p.E129Q; 17:39742976-39742976 |
breast | carcinoma | Substitution - Missense |
c.1225C>T; p.R409C; 17:39745743-39745743 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.795C>A; p.T265T; 17:39744201-39744201 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1145G>A; p.G382E; 17:39745474-39745474 |
skin | malignant_melanoma | Substitution - Missense |
c.838G>A; p.E280K; 17:39744589-39744589 |
skin | malignant_melanoma | Substitution - Missense |
c.1156G>C; p.E386Q; 17:39745485-39745485 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1156G>C; p.E386Q; 17:39745485-39745485 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - Missense |
c.770G>T; p.G257V; 17:39744176-39744176 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.409G>A; p.A137T; 17:39743000-39743000 |
upper_aerodigestive_tract; pharynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.409G>A; p.A137T; 17:39743000-39743000 |
breast | carcinoma | Substitution - Missense |
c.1407C>T; p.L469L; 17:39746157-39746157 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.616_625del10; p.S206fs*16; 17:39743423-39743432 |
lung | carcinoma; small_cell_carcinoma | Deletion - Frameshift |
c.34A>G; p.S12G; 17:39742335-39742335 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.809G>A; p.R270K; 17:39744560-39744560 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.172G>T; p.E58*; 17:39742582-39742582 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.165A>T; p.R55R; 17:39742575-39742575 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.716G>T; p.R239L; 17:39744122-39744122 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2T>C; p.M1T; 17:39742303-39742303 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.246A>C; p.P82P; 17:39742656-39742656 |
thyroid | other; neoplasm | Substitution - coding silent |
c.246A>C; p.P82P; 17:39742656-39742656 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.228T>G; p.S76R; 17:39742638-39742638 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.286C>T; p.R96C; 17:39742696-39742696 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.23C>T; p.P8L; 17:39742324-39742324 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1313G>A; p.R438H; 17:39745955-39745955 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.42G>A; p.P14P; 17:39742343-39742343 |
skin | malignant_melanoma | Substitution - coding silent |
c.1073G>C; p.C358S; 17:39745304-39745304 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.328G>A; p.D110N; 17:39742919-39742919 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.625G>A; p.D209N; 17:39743432-39743432 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.987G>T; p.W329C; 17:39744960-39744960 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1461G>A; p.E487E; 17:39746759-39746759 |
skin; arm | malignant_melanoma | Substitution - coding silent |
c.1461G>A; p.E487E; 17:39746759-39746759 |
skin | malignant_melanoma | Substitution - coding silent |
c.258C>T; p.G86G; 17:39742668-39742668 |
skin | malignant_melanoma | Substitution - coding silent |
c.680G>A; p.G227D; 17:39744086-39744086 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.947G>A; p.R316Q; 17:39744920-39744920 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.947G>A; p.R316Q; 17:39744920-39744920 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.767C>G; p.S256C; 17:39744173-39744173 |
breast | carcinoma; HER-positive_carcinoma | Substitution - Missense |
c.1299C>A; p.H433Q; 17:39745941-39745941 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.656T>C; p.L219P; 17:39743463-39743463 |
skin | malignant_melanoma | Substitution - Missense |
c.1260C>A; p.S420R; 17:39745778-39745778 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.86G>A; p.R29Q; 17:39742387-39742387 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1082C>T; p.S361F; 17:39745313-39745313 |
thyroid | carcinoma | Substitution - Missense |
c.1163C>T; p.P388L; 17:39745492-39745492 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.657C>T; p.L219L; 17:39743464-39743464 |
skin | malignant_melanoma | Substitution - coding silent |
c.113_121delAGGTAAAGA; p.E38_R41>G; 17:39742414-39742422 |
stomach | carcinoma; intestinal_adenocarcinoma | Complex - deletion inframe |
c.189C>T; p.S63S; 17:39742599-39742599 |
skin | malignant_melanoma | Substitution - coding silent |
c.208_209CC>TT; p.P70F; 17:39742618-39742619 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.761G>A; p.R254H; 17:39744167-39744167 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.761G>A; p.R254H; 17:39744167-39744167 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1432A>C; p.K478Q; 17:39746182-39746182 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1432A>C; p.K478Q; 17:39746182-39746182 |
liver | carcinoma | Substitution - Missense |
c.624C>T; p.L208L; 17:39743431-39743431 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.217G>A; p.E73K; 17:39742627-39742627 |
skin | malignant_melanoma | Substitution - Missense |
c.1011+3G>C; p.?; 17:39744987-39744987 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Unknown |
c.1045G>A; p.A349T; 17:39745276-39745276 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1A>G; p.M1V; 17:39742302-39742302 |
liver | carcinoma | Substitution - Missense |
c.1445T>C; p.I482T; 17:39746195-39746195 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.185C>T; p.T62I; 17:39742595-39742595 |
skin | malignant_melanoma | Substitution - Missense |
c.917A>G; p.N306S; 17:39744890-39744890 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.164G>A; p.R55Q; 17:39742574-39742574 |
breast | carcinoma | Substitution - Missense |
c.1070C>G; p.S357C; 17:39745301-39745301 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1251C>T; p.S417S; 17:39745769-39745769 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.869G>A; p.R290H; 17:39744620-39744620 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1055G>A; p.R352H; 17:39745286-39745286 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.392T>A; p.L131Q; 17:39742983-39742983 |
breast | carcinoma | Substitution - Missense |
c.1270G>A; p.A424T; 17:39745788-39745788 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.590C>T; p.S197F; 17:39743397-39743397 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1202C>T; p.A401V; 17:39745531-39745531 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.379G>A; p.V127M; 17:39742970-39742970 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1241T>C; p.M414T; 17:39745759-39745759 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.443G>T; p.C148F; 17:39743034-39743034 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.414G>C; p.L138F; 17:39743005-39743005 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1119G>A; p.V373V; 17:39745448-39745448 |
skin | malignant_melanoma | Substitution - coding silent |
c.410C>T; p.A137V; 17:39743001-39743001 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.537C>T; p.F179F; 17:39743253-39743253 |
ovary | other; neoplasm | Substitution - coding silent |
c.537C>T; p.F179F; 17:39743253-39743253 |
skin | malignant_melanoma | Substitution - coding silent |
c.870C>T; p.R290R; 17:39744621-39744621 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1094G>T; p.R365I; 17:39745423-39745423 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.663G>T; p.Q221H; 17:39743470-39743470 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.57A>G; p.P19P; 17:39742358-39742358 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.120G>C; p.K40N; 17:39742421-39742421 |
breast | carcinoma | Substitution - Missense |
c.372T>A; p.A124A; 17:39742963-39742963 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1108A>G; p.N370D; 17:39745437-39745437 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.847G>A; p.V283M; 17:39744598-39744598 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1460A>C; p.E487A; 17:39746758-39746758 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.546G>A; p.R182R; 17:39743262-39743262 |
skin | malignant_melanoma | Substitution - coding silent |
c.287delG; p.R96fs*8; 17:39742697-39742697 |
lung | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1115T>C; p.L372P; 17:39745444-39745444 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.583C>T; p.P195S; 17:39743299-39743299 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1304G>A; p.R435H; 17:39745946-39745946 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1304G>A; p.R435H; 17:39745946-39745946 |
prostate | carcinoma | Substitution - Missense |
c.1304G>A; p.R435H; 17:39745946-39745946 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.1304G>A; p.R435H; 17:39745946-39745946 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1309T>C; p.S437P; 17:39745951-39745951 |
skin | malignant_melanoma | Substitution - Missense |
c.892G>A; p.D298N; 17:39744643-39744643 |
skin | malignant_melanoma | Substitution - Missense |
c.188C>T; p.S63F; 17:39742598-39742598 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.532C>T; p.R178C; 17:39743248-39743248 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1046_1047delCA; p.Q350fs*20; 17:39745277-39745278 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - Frameshift |
c.1454G>A; p.S485N; 17:39746752-39746752 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.776A>G; p.Y259C; 17:39744182-39744182 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |