| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 6195 |
Name | RPS6KA1 |
Synonymous | ribosomal protein S6 kinase, 90kDa, polypeptide 1;RPS6KA1;ribosomal protein S6 kinase, 90kDa, polypeptide 1 |
Definition | 90 kDa ribosomal protein S6 kinase 1|MAP kinase-activated protein kinase 1a|MAPK-activated protein kinase 1a|MAPKAP kinase 1a|MAPKAPK-1a|RSK-1|S6K-alpha 1|S6K-alpha-1|dJ590P13.1 (ribosomal protein S6 kinase, 90kD, polypeptide 1)|p90-RSK 1|p90RSK1|p90S6K|r |
Position | 1p |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1236G>T; p.L412L; 1:26560746-26560746 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1615A>T; p.S539C; 1:26571473-26571473 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1301G>A; p.R434H; 1:26560811-26560811 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.669C>T; p.C223C; 1:26554651-26554651 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2131A>C; p.T711P; 1:26574124-26574124 |
breast | carcinoma | Substitution - Missense |
c.346C>T; p.L116L; 1:26551435-26551435 |
skin | malignant_melanoma | Substitution - coding silent |
c.516T>C; p.A172A; 1:26553438-26553438 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.350C>A; p.A117D; 1:26551439-26551439 |
thyroid | other; neoplasm | Substitution - Missense |
c.881G>A; p.R294Q; 1:26555590-26555590 |
breast | carcinoma | Substitution - Missense |
c.1181G>T; p.R394L; 1:26558903-26558903 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.336G>A; p.E112E; 1:26551425-26551425 |
oesophagus | carcinoma | Substitution - coding silent |
c.1098delC; p.S369fs*18; 1:26558820-26558820 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1098delC; p.S369fs*18; 1:26558820-26558820 |
NS | malignant_melanoma | Deletion - Frameshift |
c.1098delC; p.S369fs*18; 1:26558820-26558820 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1423C>T; p.L475L; 1:26561126-26561126 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1849G>A; p.G617S; 1:26572195-26572195 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.175C>T; p.P59S; 1:26546933-26546933 |
skin | malignant_melanoma | Substitution - Missense |
c.1592T>C; p.V531A; 1:26571450-26571450 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2134C>T; p.P712S; 1:26574127-26574127 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.369C>T; p.F123F; 1:26551458-26551458 |
skin | malignant_melanoma | Substitution - coding silent |
c.1785C>T; p.C595C; 1:26571881-26571881 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1002C>G; p.I334M; 1:26557018-26557018 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.101C>T; p.P34L; 1:26536962-26536962 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.323G>A; p.R108Q; 1:26551412-26551412 |
skin | malignant_melanoma | Substitution - Missense |
c.1177C>A; p.P393T; 1:26558899-26558899 |
thyroid | other; neoplasm | Substitution - Missense |
c.2102C>T; p.T701M; 1:26574095-26574095 |
skin | malignant_melanoma | Substitution - Missense |
c.1170C>T; p.D390D; 1:26558892-26558892 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1437T>C; p.Y479Y; 1:26561510-26561510 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.51T>G; p.P17P; 1:26529971-26529971 |
thyroid | other; neoplasm | Substitution - coding silent |
c.2159C>G; p.S720C; 1:26574152-26574152 |
skin | malignant_melanoma | Substitution - Missense |
c.443A>T; p.D148V; 1:26551698-26551698 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1508G>A; p.R503Q; 1:26561581-26561581 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.147C>T; p.H49H; 1:26546905-26546905 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.118G>A; p.V40I; 1:26546876-26546876 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1848C>T; p.N616N; 1:26572194-26572194 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.706C>T; p.R236C; 1:26554688-26554688 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.706C>T; p.R236C; 1:26554688-26554688 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2155T>C; p.S719P; 1:26574148-26574148 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.831G>A; p.A277A; 1:26555540-26555540 |
breast | carcinoma | Substitution - coding silent |
c.1591G>T; p.V531F; 1:26571449-26571449 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.995G>A; p.R332H; 1:26557011-26557011 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.134C>T; p.S45F; 1:26546892-26546892 |
skin | malignant_melanoma | Substitution - Missense |
c.506C>T; p.A169V; 1:26553428-26553428 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1601G>T; p.R534M; 1:26571459-26571459 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1641C>T; p.S547S; 1:26571499-26571499 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.993T>C; p.R331R; 1:26557009-26557009 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1205C>T; p.S402L; 1:26558927-26558927 |
skin | malignant_melanoma | Substitution - Missense |
c.994C>T; p.R332C; 1:26557010-26557010 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1485G>A; p.G495G; 1:26561558-26561558 |
skin | malignant_melanoma | Substitution - coding silent |
c.1559G>A; p.G520D; 1:26561632-26561632 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1763G>T; p.R588L; 1:26571859-26571859 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.321C>T; p.V107V; 1:26551410-26551410 |
skin | malignant_melanoma | Substitution - coding silent |
c.124A>G; p.K42E; 1:26546882-26546882 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1197C>T; p.P399P; 1:26558919-26558919 |
skin | malignant_melanoma | Substitution - coding silent |
c.1809G>T; p.L603L; 1:26571905-26571905 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.878T>C; p.L293S; 1:26555587-26555587 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2044C>T; p.P682S; 1:26573320-26573320 |
skin | malignant_melanoma | Substitution - Missense |
c.2044C>T; p.P682S; 1:26573320-26573320 |
skin | malignant_melanoma | Substitution - Missense |
c.2044C>T; p.P682S; 1:26573320-26573320 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.924C>T; p.G308G; 1:26556661-26556661 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1044_1046delCTT; p.F349delF; 1:26557060-26557062 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - In frame |
c.1370C>T; p.S457L; 1:26561073-26561073 |
breast | carcinoma | Substitution - Missense |
c.1882C>T; p.R628W; 1:26572228-26572228 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.773G>A; p.G258D; 1:26555167-26555167 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1100C>G; p.P367R; 1:26558822-26558822 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.100C>T; p.P34S; 1:26536961-26536961 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.1168G>A; p.D390N; 1:26558890-26558890 |
breast | carcinoma | Substitution - Missense |
c.1070C>T; p.S357F; 1:26557086-26557086 |
skin | malignant_melanoma | Substitution - Missense |
c.771G>A; p.T257T; 1:26555165-26555165 |
skin | malignant_melanoma | Substitution - coding silent |
c.1588G>C; p.G530R; 1:26561661-26561661 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1706G>A; p.G569E; 1:26571564-26571564 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1357A>C; p.K453Q; 1:26561060-26561060 |
liver | carcinoma | Substitution - Missense |
c.1398T>C; p.Y466Y; 1:26561101-26561101 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1357A>C; p.K453Q; 1:26561060-26561060 |
liver | carcinoma | Substitution - Missense |
c.1152C>T; p.T384T; 1:26558874-26558874 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1152C>T; p.T384T; 1:26558874-26558874 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.2101A>C; p.T701P; 1:26574094-26574094 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.989A>G; p.Y330C; 1:26557005-26557005 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.192C>T; p.L64L; 1:26546950-26546950 |
skin | malignant_melanoma | Substitution - coding silent |
c.1180C>T; p.R394C; 1:26558902-26558902 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1838C>T; p.P613L; 1:26572184-26572184 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.246C>T; p.V82V; 1:26547209-26547209 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1407C>T; p.H469H; 1:26561110-26561110 |
skin | malignant_melanoma | Substitution - coding silent |
c.108G>T; p.K36N; 1:26536969-26536969 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.595G>A; p.G199S; 1:26554233-26554233 |
ovary | other; neoplasm | Substitution - Missense |
c.1657C>T; p.L553L; 1:26571515-26571515 |
skin | malignant_melanoma | Substitution - coding silent |
c.770C>T; p.T257M; 1:26555164-26555164 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1544T>A; p.V515D; 1:26561617-26561617 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.559G>A; p.D187N; 1:26553481-26553481 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1097T>C; p.I366T; 1:26558819-26558819 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.1798C>T; p.L600L; 1:26571894-26571894 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1798C>T; p.L600L; 1:26571894-26571894 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.1529G>A; p.R510Q; 1:26561602-26561602 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1004A>C; p.K335T; 1:26557020-26557020 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.798C>T; p.D266D; 1:26555192-26555192 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1352A>T; p.K451M; 1:26561055-26561055 |
skin | malignant_melanoma | Substitution - Missense |
c.239G>A; p.R80Q; 1:26547202-26547202 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |