| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 6464 |
Name | SHC1 |
Synonymous | SHC (Src homology 2 domain containing) transforming protein 1;SHC1;SHC (Src homology 2 domain containing) transforming protein 1 |
Definition | SH2 domain protein C1|SHC (Src homology 2 domain-containing) transforming protein 1|SHC-transforming protein 1|SHC-transforming protein 3|SHC-transforming protein A |
Position | 1q21 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1379C>T; p.A460V; 1:154963849-154963849 |
pancreas | carcinoma | Substitution - Missense |
c.1379C>T; p.A460V; 1:154963849-154963849 |
pancreas | carcinoid-endocrine_tumour | Substitution - Missense |
c.982C>T; p.R328W; 1:154966021-154966021 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.982C>T; p.R328W; 1:154966021-154966021 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1204C>A; p.R402R; 1:154965635-154965635 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1066G>A; p.E356K; 1:154965773-154965773 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.873G>A; p.G291G; 1:154966211-154966211 |
bone; femur | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1261C>T; p.P421S; 1:154965578-154965578 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.78C>G; p.R26R; 1:154970119-154970119 |
skin | malignant_melanoma | Substitution - coding silent |
c.787G>A; p.A263T; 1:154966384-154966384 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - Missense |
c.605T>C; p.F202S; 1:154967719-154967719 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.63C>T; p.G21G; 1:154970134-154970134 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1291G>C; p.G431R; 1:154965548-154965548 |
liver | carcinoma | Substitution - Missense |
c.1291G>C; p.G431R; 1:154965548-154965548 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.381C>A; p.S127S; 1:154968534-154968534 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1293T>G; p.G431G; 1:154965546-154965546 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.406G>A; p.A136T; 1:154968509-154968509 |
thyroid | carcinoma | Substitution - Missense |
c.1422G>A; p.L474L; 1:154963806-154963806 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1415G>A; p.R472Q; 1:154963813-154963813 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.420G>T; p.Q140H; 1:154968495-154968495 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.670G>T; p.G224C; 1:154966501-154966501 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.670G>T; p.G224C; 1:154966501-154966501 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - Missense |
c.869T>C; p.V290A; 1:154966215-154966215 |
skin | malignant_melanoma | Substitution - Missense |
c.999T>G; p.G333G; 1:154966004-154966004 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.1039C>T; p.R347W; 1:154965964-154965964 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1039C>T; p.R347W; 1:154965964-154965964 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.951C>A; p.S317S; 1:154966052-154966052 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.800C>T; p.A267V; 1:154966371-154966371 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.983G>A; p.R328Q; 1:154966020-154966020 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.376G>A; p.V126I; 1:154968539-154968539 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - Missense |
c.829C>T; p.P277S; 1:154966342-154966342 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.25G>A; p.G9R; 1:154970172-154970172 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.649G>C; p.D217H; 1:154967675-154967675 |
prostate | adenoma | Substitution - Missense |
c.187C>A; p.L63I; 1:154969427-154969427 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.699G>T; p.E233D; 1:154966472-154966472 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.286A>C; p.T96P; 1:154968785-154968785 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.196delA; p.M66fs*50; 1:154969418-154969418 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Deletion - Frameshift |
c.898A>G; p.M300V; 1:154966186-154966186 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1200G>A; p.L400L; 1:154965639-154965639 |
breast | carcinoma | Substitution - coding silent |
c.1387G>A; p.E463K; 1:154963841-154963841 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.850T>C; p.L284L; 1:154966321-154966321 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.785_786CC>TT; p.A262V; 1:154966385-154966386 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.729C>A; p.F243L; 1:154966442-154966442 |
skin | malignant_melanoma | Substitution - Missense |
c.889C>T; p.R297C; 1:154966195-154966195 |
endometrium | carcinoma; serous_carcinoma | Substitution - Missense |
c.106C>T; p.R36W; 1:154970091-154970091 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.919C>G; p.P307A; 1:154966165-154966165 |
skin; upper_leg | malignant_melanoma | Substitution - Missense |
c.950C>G; p.S317C; 1:154966053-154966053 |
breast | carcinoma | Substitution - Missense |
c.721A>T; p.N241Y; 1:154966450-154966450 |
liver | carcinoma | Substitution - Missense |
c.721A>T; p.N241Y; 1:154966450-154966450 |
liver | carcinoma | Substitution - Missense |
c.200G>A; p.R67H; 1:154969414-154969414 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1080C>G; p.R360R; 1:154965759-154965759 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.677C>T; p.A226V; 1:154966494-154966494 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.100C>T; p.P34S; 1:154970097-154970097 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.639C>T; p.V213V; 1:154967685-154967685 |
prostate | carcinoma | Substitution - coding silent |
c.538C>G; p.L180V; 1:154967786-154967786 |
ovary | other; neoplasm | Substitution - Missense |
c.1093C>T; p.P365S; 1:154965746-154965746 |
skin | malignant_melanoma | Substitution - Missense |
c.1093C>T; p.P365S; 1:154965746-154965746 |
skin | malignant_melanoma | Substitution - Missense |
c.1155C>G; p.S385R; 1:154965684-154965684 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1366C>T; p.P456S; 1:154963862-154963862 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.637G>C; p.V213L; 1:154967687-154967687 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.73A>C; p.T25P; 1:154970124-154970124 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.73A>C; p.T25P; 1:154970124-154970124 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.73A>C; p.T25P; 1:154970124-154970124 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.73A>C; p.T25P; 1:154970124-154970124 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.73A>C; p.T25P; 1:154970124-154970124 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.755G>T; p.G252V; 1:154966416-154966416 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.284C>T; p.A95V; 1:154968787-154968787 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.364A>G; p.I122V; 1:154968551-154968551 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.393C>T; p.L131L; 1:154968522-154968522 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.594C>T; p.F198F; 1:154967730-154967730 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.594C>T; p.F198F; 1:154967730-154967730 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.890G>A; p.R297H; 1:154966194-154966194 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.700C>T; p.P234S; 1:154966471-154966471 |
skin | malignant_melanoma | Substitution - Missense |
c.375C>A; p.T125T; 1:154968540-154968540 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.122C>T; p.P41L; 1:154970075-154970075 |
skin | malignant_melanoma | Substitution - Missense |
c.757_758insG; p.V253fs*62; 1:154966413-154966414 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Insertion - Frameshift |
c.757delG; p.V253fs*2; 1:154966414-154966414 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1101G>C; p.S367S; 1:154965738-154965738 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.757delG; p.V253fs*2; 1:154966414-154966414 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.757delG; p.V253fs*2; 1:154966414-154966414 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.757_758insG; p.V253fs*62; 1:154966413-154966414 |
large_intestine; caecum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.757_758insG; p.V253fs*62; 1:154966413-154966414 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.757delG; p.V253fs*2; 1:154966414-154966414 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.285G>T; p.A95A; 1:154968786-154968786 |
skin | malignant_melanoma | Substitution - coding silent |
c.1089A>C; p.P363P; 1:154965750-154965750 |
pancreas | carcinoma | Substitution - coding silent |
c.1315C>T; p.R439C; 1:154963913-154963913 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1078C>T; p.R360C; 1:154965761-154965761 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |