General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 6850 |
Name | SYK |
Synonymous | spleen tyrosine kinase;SYK;spleen tyrosine kinase |
Definition | tyrosine-protein kinase SYK |
Position | 9q22 |
Gene Type | protein-coding |
Mutation summary: | Mutations in domains Mutational pattern in 17 major cancer types LoF vs missense mutations All the copy number variations from COSMIC database V72 All the mutations from COSMIC database V72 |
Mutation summary in protein domains | Top |
The non-synonymous (top) and synonymous (bottom) mutational percentage for various cancers | Top |
Loss of Function mutations compare to missense mutations | Top |
The ratio of the loss-of-function mutations over missense mutations is 0.12. |
The copy number variations for various cancers | Top |
The copy number variations in 17 major cancer types: 1; Breast, 2; Central nervous system, 3; Cervix, 4; Endometrium, 5; Haematopoietic and lymphoid_tissue, 6; Kidney, 7; Large intestine, 8; Liver, 9; Lung, 10; Not specific, 11; Ovary, 12; Pancreas, 13; Prostate, 14; Skin, 15; Stomach, 16; Thyroid, 17; Urinary tract |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) |
Site |
Histology |
Mutation Type |
---|---|---|---|
c.1738G>A; p.D580N; 9:90888599-90888599 |
skin | malignant_melanoma | Substitution - Missense |
c.1255G>A; p.E419K; 9:90877713-90877713 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.1738G>A; p.D580N; 9:90888599-90888599 |
skin | malignant_melanoma | Substitution - Missense |
c.988G>A; p.A330T; 9:90874725-90874725 |
liver | carcinoma | Substitution - Missense |
c.988G>A; p.A330T; 9:90874725-90874725 |
prostate | carcinoma | Substitution - Missense |
c.988G>A; p.A330T; 9:90874725-90874725 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.988G>A; p.A330T; 9:90874725-90874725 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.988G>A; p.A330T; 9:90874725-90874725 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.988G>A; p.A330T; 9:90874725-90874725 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.988G>A; p.A330T; 9:90874725-90874725 |
liver | carcinoma | Substitution - Missense |
c.988G>A; p.A330T; 9:90874725-90874725 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1811G>A; p.R604H; 9:90895572-90895572 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1043C>T; p.T348M; 9:90874780-90874780 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.82T>G; p.Y28D; 9:90843980-90843980 |
breast | carcinoma | Substitution - Missense |
c.1432T>C; p.L478L; 9:90878873-90878873 |
liver | carcinoma | Substitution - coding silent |
c.1432T>C; p.L478L; 9:90878873-90878873 |
liver | carcinoma | Substitution - coding silent |
c.131G>T; p.S44I; 9:90844029-90844029 |
liver | carcinoma | Substitution - Missense |
c.1031G>A; p.R344Q; 9:90874768-90874768 |
pancreas | carcinoma | Substitution - Missense |
c.1368C>T; p.S456S; 9:90878809-90878809 |
skin | malignant_melanoma | Substitution - coding silent |
c.1368C>T; p.S456S; 9:90878809-90878809 |
skin | malignant_melanoma | Substitution - coding silent |
c.975C>T; p.Y325Y; 9:90874712-90874712 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.437C>G; p.A146G; 9:90845453-90845453 |
breast | carcinoma | Substitution - Missense |
c.66G>A; p.R22R; 9:90843964-90843964 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.1546T>A; p.Y516N; 9:90887782-90887782 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; follicular_lymphoma | Substitution - Missense |
c.1828G>A; p.V610M; 9:90895589-90895589 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1367C>T; p.S456F; 9:90878808-90878808 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1637G>T; p.G546V; 9:90887873-90887873 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1241G>A; p.G414E; 9:90877699-90877699 |
skin | malignant_melanoma | Substitution - Missense |
c.602G>A; p.G201D; 9:90862229-90862229 |
liver | carcinoma | Substitution - Missense |
c.1014G>T; p.K338N; 9:90874751-90874751 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1465G>A; p.D489N; 9:90878906-90878906 |
skin | malignant_melanoma | Substitution - Missense |
c.1737C>T; p.Y579Y; 9:90888598-90888598 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1372G>A; p.G458S; 9:90878813-90878813 |
skin | malignant_melanoma | Substitution - Missense |
c.313A>G; p.K105E; 9:90844211-90844211 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.702C>T; p.F234F; 9:90862329-90862329 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.702C>T; p.F234F; 9:90862329-90862329 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.702C>T; p.F234F; 9:90862329-90862329 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1121A>C; p.K374T; 9:90877579-90877579 |
liver | carcinoma | Substitution - Missense |
c.922G>T; p.A308S; 9:90874279-90874279 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.583C>T; p.R195*; 9:90862210-90862210 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1470C>T; p.F490F; 9:90878911-90878911 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1105A>C; p.M369L; 9:90874842-90874842 |
liver | carcinoma | Substitution - Missense |
c.1105A>C; p.M369L; 9:90874842-90874842 |
liver | carcinoma | Substitution - Missense |
c.960G>A; p.M320I; 9:90874697-90874697 |
skin | malignant_melanoma | Substitution - Missense |
c.1738G>C; p.D580H; 9:90888599-90888599 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1584C>T; p.S528S; 9:90887820-90887820 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.877A>T; p.S293C; 9:90874234-90874234 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.655G>A; p.D219N; 9:90862282-90862282 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.267C>T; p.C89C; 9:90844165-90844165 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.913G>A; p.A305T; 9:90874270-90874270 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1407C>G; p.H469Q; 9:90878848-90878848 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; polycythaemia_vera | Substitution - Missense |
c.1428T>C; p.N476N; 9:90878869-90878869 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.1664G>A; p.G555E; 9:90888525-90888525 |
skin | malignant_melanoma | Substitution - Missense |
c.1428T>C; p.N476N; 9:90878869-90878869 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1664G>A; p.G555E; 9:90888525-90888525 |
skin | malignant_melanoma | Substitution - Missense |
c.1664G>A; p.G555E; 9:90888525-90888525 |
skin | malignant_melanoma | Substitution - Missense |
c.1213G>A; p.D405N; 9:90877671-90877671 |
skin | malignant_melanoma | Substitution - Missense |
c.1635T>G; p.Y545*; 9:90887871-90887871 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1233G>C; p.R411R; 9:90877691-90877691 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1655G>A; p.G552E; 9:90888516-90888516 |
skin | malignant_melanoma | Substitution - Missense |
c.1233G>C; p.R411R; 9:90877691-90877691 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1635T>G; p.Y545*; 9:90887871-90887871 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1213G>A; p.D405N; 9:90877671-90877671 |
ovary | other; neoplasm | Substitution - Missense |
c.93delG; p.G33fs*2; 9:90843991-90843991 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.717+1G>A; p.?; 9:90862345-90862345 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Unknown |
c.315G>T; p.K105N; 9:90844213-90844213 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.936C>A; p.G312G; 9:90874673-90874673 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.965C>G; p.T322R; 9:90874702-90874702 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.958A>T; p.M320L; 9:90874695-90874695 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1120A>G; p.K374E; 9:90877578-90877578 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1092G>T; p.K364N; 9:90874829-90874829 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.457C>T; p.Q153*; 9:90845473-90845473 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1700G>A; p.R567Q; 9:90888561-90888561 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.525G>T; p.R175R; 9:90845541-90845541 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.852C>T; p.S284S; 9:90874209-90874209 |
skin | malignant_melanoma | Substitution - coding silent |
c.851C>T; p.S284F; 9:90874208-90874208 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.297G>T; p.L99L; 9:90844195-90844195 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1796T>C; p.V599A; 9:90895557-90895557 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.297G>T; p.L99L; 9:90844195-90844195 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - coding silent |
c.647A>G; p.Y216C; 9:90862274-90862274 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.311A>G; p.K104R; 9:90844209-90844209 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.685C>T; p.P229S; 9:90862312-90862312 |
skin; trunk | malignant_melanoma; nodular | Substitution - Missense |
c.778C>T; p.Q260*; 9:90864649-90864649 |
skin | malignant_melanoma | Substitution - Nonsense |
c.465G>A; p.E155E; 9:90845481-90845481 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1535C>T; p.P512L; 9:90887771-90887771 |
skin | malignant_melanoma | Substitution - Missense |
c.1443C>T; p.T481T; 9:90878884-90878884 |
skin | malignant_melanoma | Substitution - coding silent |
c.465G>A; p.E155E; 9:90845481-90845481 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - coding silent |
c.1750C>T; p.L584L; 9:90888611-90888611 |
skin | malignant_melanoma | Substitution - coding silent |
c.1314G>A; p.Q438Q; 9:90877772-90877772 |
skin | malignant_melanoma | Substitution - coding silent |
c.1675A>G; p.T559A; 9:90888536-90888536 |
pancreas | carcinoma | Substitution - Missense |
c.1675A>G; p.T559A; 9:90888536-90888536 |
pancreas | carcinoma | Substitution - Missense |
c.154G>A; p.A52T; 9:90844052-90844052 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.274C>T; p.H92Y; 9:90844172-90844172 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.832G>A; p.G278S; 9:90865083-90865083 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.649C>T; p.R217C; 9:90862276-90862276 |
skin | malignant_melanoma | Substitution - Missense |
c.971T>G; p.V324G; 9:90874708-90874708 |
breast | carcinoma | Substitution - Missense |
c.254C>T; p.P85L; 9:90844152-90844152 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.259G>T; p.D87Y; 9:90844157-90844157 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.897G>A; p.P299P; 9:90874254-90874254 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.897G>A; p.P299P; 9:90874254-90874254 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1452C>T; p.Y484Y; 9:90878893-90878893 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1452C>T; p.Y484Y; 9:90878893-90878893 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1476T>C; p.L492L; 9:90878917-90878917 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1669G>A; p.E557K; 9:90888530-90888530 |
skin | malignant_melanoma | Substitution - Missense |
c.92_93insG; p.M34fs*3; 9:90843990-90843991 |
large_intestine | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.92_93insG; p.M34fs*3; 9:90843990-90843991 |
large_intestine | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1048G>T; p.E350*; 9:90874785-90874785 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1113-7C>G; p.?; 9:90877564-90877564 |
liver | carcinoma; hepatocellular_carcinoma | Unknown |
c.1269G>A; p.L423L; 9:90877727-90877727 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1512G>T; p.K504N; 9:90878953-90878953 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1269G>A; p.L423L; 9:90877727-90877727 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.862G>A; p.G288R; 9:90874219-90874219 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.76G>A; p.E26K; 9:90843974-90843974 |
liver | carcinoma | Substitution - Missense |
c.76G>A; p.E26K; 9:90843974-90843974 |
liver | carcinoma | Substitution - Missense |
c.76G>A; p.E26K; 9:90843974-90843974 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1248C>G; p.C416W; 9:90877706-90877706 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1651C>T; p.R551*; 9:90887887-90887887 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1799A>G; p.E600G; 9:90895560-90895560 |
breast | carcinoma | Substitution - Missense |
c.1651C>T; p.R551*; 9:90887887-90887887 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1097A>G; p.Y366C; 9:90874834-90874834 |
liver | carcinoma | Substitution - Missense |
c.1097A>G; p.Y366C; 9:90874834-90874834 |
liver | carcinoma | Substitution - Missense |
c.1144delA; p.N383fs*13; 9:90877602-90877602 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.215G>A; p.G72D; 9:90844113-90844113 |
skin | malignant_melanoma | Substitution - Missense |
c.108T>C; p.D36D; 9:90844006-90844006 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.737A>G; p.Y246C; 9:90864608-90864608 |
stomach | carcinoma | Substitution - Missense |
c.153C>T; p.F51F; 9:90844051-90844051 |
skin | malignant_melanoma | Substitution - coding silent |
c.490_491insA; p.M166fs*14; 9:90845506-90845507 |
large_intestine; rectum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.125G>A; p.R42H; 9:90844023-90844023 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.973T>C; p.Y325H; 9:90874710-90874710 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; hairy_cell_leukaemia | Substitution - Missense |
c.854C>A; p.P285H; 9:90874211-90874211 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1273A>T; p.M425L; 9:90877731-90877731 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1706G>T; p.G569V; 9:90888567-90888567 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.810T>G; p.F270L; 9:90865061-90865061 |
skin | malignant_melanoma | Substitution - Missense |
c.810T>G; p.F270L; 9:90865061-90865061 |
skin | malignant_melanoma | Substitution - Missense |
c.944G>A; p.R315K; 9:90874681-90874681 |
skin | malignant_melanoma | Substitution - Missense |
c.1810C>T; p.R604C; 9:90895571-90895571 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1142T>C; p.L381P; 9:90877600-90877600 |
skin | malignant_melanoma | Substitution - Missense |
c.134G>A; p.R45H; 9:90844032-90844032 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.962A>G; p.D321G; 9:90874699-90874699 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.534T>C; p.S178S; 9:90845550-90845550 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1596C>G; p.V532V; 9:90887832-90887832 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1469T>G; p.F490C; 9:90878910-90878910 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1239C>T; p.I413I; 9:90877697-90877697 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1113-1G>C; p.?; 9:90877570-90877570 |
ovary | carcinoma; serous_carcinoma | Unknown |
c.921G>T; p.W307C; 9:90874278-90874278 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1700_1701GG>AC; p.R567H; 9:90888561-90888562 |
skin | malignant_melanoma | Substitution - Missense |
c.1548C>T; p.Y516Y; 9:90887784-90887784 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1548C>T; p.Y516Y; 9:90887784-90887784 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1206G>T; p.Q402H; 9:90877664-90877664 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1625C>T; p.A542V; 9:90887861-90887861 |
skin | malignant_melanoma | Substitution - Missense |
c.176G>A; p.R59K; 9:90844074-90844074 |
large_intestine; colon | adenoma | Substitution - Missense |
c.1625C>T; p.A542V; 9:90887861-90887861 |
skin | malignant_melanoma | Substitution - Missense |
c.1809G>A; p.L603L; 9:90895570-90895570 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.272A>G; p.Y91C; 9:90844170-90844170 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.173G>A; p.G58E; 9:90844071-90844071 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1283C>T; p.A428V; 9:90877741-90877741 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.996C>T; p.P332P; 9:90874733-90874733 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.298G>T; p.V100F; 9:90844196-90844196 |
thyroid | other; neoplasm | Substitution - Missense |
c.1772A>G; p.E591G; 9:90895533-90895533 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1220C>T; p.P407L; 9:90877678-90877678 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1015G>A; p.E339K; 9:90874752-90874752 |
skin | malignant_melanoma | Substitution - Missense |
c.702C>A; p.F234L; 9:90862329-90862329 |
central_nervous_system; frontal_lobe | glioma; astrocytoma_Grade_IV | Substitution - Missense |