General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 90627 |
Name | STARD13 |
Synonymous | StAR-related lipid transfer (START) domain containing 13;STARD13;StAR-related lipid transfer (START) domain containing 13 |
Definition | Rho GTPase activating protein on chromosome 13q12|deleted in liver cancer 2 protein|long intergenic non-protein coding RNA 464|stAR-related lipid transfer protein 13 |
Position | 13q13.1 |
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 0.09. |
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.2544C>G; p.N848K; 13:33111841-33111841 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.601G>A; p.E201K; 13:33130076-33130076 |
skin | malignant_melanoma | Substitution - Missense |
c.2382C>T; p.N794N; 13:33112831-33112831 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2036G>T; p.S679I; 13:33126127-33126127 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.696C>T; p.L232L; 13:33129981-33129981 |
skin | malignant_melanoma | Substitution - coding silent |
c.234A>C; p.L78F; 13:33167558-33167558 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.368T>A; p.V123E; 13:33142329-33142329 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1841G>A; p.S614N; 13:33127454-33127454 |
skin | malignant_melanoma | Substitution - Missense |
c.367G>T; p.V123L; 13:33142330-33142330 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3301T>C; p.F1101L; 13:33105634-33105634 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.381G>A; p.R127R; 13:33142316-33142316 |
skin | malignant_melanoma | Substitution - coding silent |
c.154A>G; p.T52A; 13:33285485-33285485 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2052G>T; p.L684L; 13:33126111-33126111 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1436A>T; p.K479I; 13:33129241-33129241 |
skin | malignant_melanoma | Substitution - Missense |
c.1976C>T; p.A659V; 13:33126187-33126187 |
skin | malignant_melanoma | Substitution - Missense |
c.295G>A; p.E99K; 13:33165365-33165365 |
skin | malignant_melanoma | Substitution - Missense |
c.1976C>T; p.A659V; 13:33126187-33126187 |
skin | malignant_melanoma | Substitution - Missense |
c.464G>T; p.R155L; 13:33130213-33130213 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.524C>T; p.T175M; 13:33130153-33130153 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1211G>A; p.G404E; 13:33129466-33129466 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1591C>G; p.Q531E; 13:33129086-33129086 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.812C>A; p.A271D; 13:33129865-33129865 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3299C>T; p.S1100F; 13:33105636-33105636 |
skin | malignant_melanoma | Substitution - Missense |
c.1410C>A; p.S470R; 13:33129267-33129267 |
kidney | other; neoplasm | Substitution - Missense |
c.520G>T; p.G174C; 13:33130157-33130157 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1311G>T; p.Q437H; 13:33129366-33129366 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.790G>A; p.E264K; 13:33129887-33129887 |
skin | malignant_melanoma | Substitution - Missense |
c.1892A>G; p.H631R; 13:33127403-33127403 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.10C>T; p.Q4*; 13:33285629-33285629 |
breast | carcinoma | Substitution - Nonsense |
c.203G>A; p.R68H; 13:33167589-33167589 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2364G>A; p.T788T; 13:33112849-33112849 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2642C>T; p.S881L; 13:33110873-33110873 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2775C>T; p.F925F; 13:33110740-33110740 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2077G>A; p.D693N; 13:33126086-33126086 |
skin | malignant_melanoma | Substitution - Missense |
c.2077G>A; p.D693N; 13:33126086-33126086 |
skin | malignant_melanoma | Substitution - Missense |
c.803G>A; p.G268E; 13:33129874-33129874 |
skin; trunk | malignant_melanoma | Substitution - Missense |
c.1090T>G; p.L364V; 13:33129587-33129587 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.3093C>T; p.S1031S; 13:33106889-33106889 |
skin | malignant_melanoma | Substitution - coding silent |
c.2905C>T; p.R969C; 13:33110015-33110015 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.837G>A; p.G279G; 13:33129840-33129840 |
skin | malignant_melanoma | Substitution - coding silent |
c.625C>T; p.R209C; 13:33130052-33130052 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.3162C>T; p.Y1054Y; 13:33106820-33106820 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1019G>A; p.S340N; 13:33129658-33129658 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3003G>A; p.L1001L; 13:33109917-33109917 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.62C>A; p.P21H; 13:33285577-33285577 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2839G>A; p.G947R; 13:33110081-33110081 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1379A>G; p.D460G; 13:33129298-33129298 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2493-1G>T; p.?; 13:33111893-33111893 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Unknown |
c.1540C>T; p.H514Y; 13:33129137-33129137 |
skin | malignant_melanoma | Substitution - Missense |
c.496G>A; p.G166R; 13:33130181-33130181 |
skin | malignant_melanoma | Substitution - Missense |
c.1439A>G; p.D480G; 13:33129238-33129238 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1721T>G; p.V574G; 13:33128956-33128956 |
skin | malignant_melanoma | Substitution - Missense |
c.2888C>A; p.P963H; 13:33110032-33110032 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.302A>G; p.D101G; 13:33165358-33165358 |
liver | carcinoma | Substitution - Missense |
c.1779G>A; p.S593S; 13:33127516-33127516 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2845C>A; p.P949T; 13:33110075-33110075 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.942G>A; p.S314S; 13:33129735-33129735 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2004C>G; p.H668Q; 13:33126159-33126159 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.494G>A; p.R165Q; 13:33130183-33130183 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.600C>T; p.S200S; 13:33130077-33130077 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.509G>T; p.G170V; 13:33130168-33130168 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2752C>T; p.Q918*; 13:33110763-33110763 |
skin; hand | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.1048G>A; p.E350K; 13:33129629-33129629 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2889delC; p.S964fs*4; 13:33110031-33110031 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1782C>T; p.H594H; 13:33127513-33127513 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3153C>A; p.D1051E; 13:33106829-33106829 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.353C>T; p.S118L; 13:33142344-33142344 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.1063G>A; p.E355K; 13:33129614-33129614 |
skin | malignant_melanoma | Substitution - Missense |
c.1449_1450CC>TT; p.P484S; 13:33129227-33129228 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2658G>A; p.E886E; 13:33110857-33110857 |
skin | malignant_melanoma | Substitution - coding silent |
c.534G>A; p.R178R; 13:33130143-33130143 |
skin | malignant_melanoma | Substitution - coding silent |
c.534G>A; p.R178R; 13:33130143-33130143 |
skin | malignant_melanoma | Substitution - coding silent |
c.2583C>T; p.I861I; 13:33111802-33111802 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.3048G>A; p.R1016R; 13:33106934-33106934 |
skin | malignant_melanoma | Substitution - coding silent |
c.2747G>A; p.G916D; 13:33110768-33110768 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1852C>T; p.R618C; 13:33127443-33127443 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.2587G>T; p.E863*; 13:33111798-33111798 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Nonsense |
c.1815C>T; p.I605I; 13:33127480-33127480 |
skin | malignant_melanoma | Substitution - coding silent |
c.1009G>A; p.E337K; 13:33129668-33129668 |
skin | malignant_melanoma | Substitution - Missense |
c.839G>T; p.R280L; 13:33129838-33129838 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.212G>C; p.G71A; 13:33167580-33167580 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.326G>T; p.R109L; 13:33142371-33142371 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.2191G>T; p.V731L; 13:33118155-33118155 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.3173C>T; p.P1058L; 13:33106809-33106809 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.660G>A; p.P220P; 13:33130017-33130017 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1722A>T; p.V574V; 13:33128955-33128955 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - coding silent |
c.2617G>A; p.E873K; 13:33110898-33110898 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2047G>T; p.A683S; 13:33126116-33126116 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3105G>A; p.E1035E; 13:33106877-33106877 |
skin | malignant_melanoma | Substitution - coding silent |
c.1519G>C; p.V507L; 13:33129158-33129158 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1926A>C; p.S642S; 13:33126237-33126237 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1926A>C; p.S642S; 13:33126237-33126237 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1641A>G; p.T547T; 13:33129036-33129036 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2122C>T; p.H708Y; 13:33118224-33118224 |
liver | carcinoma | Substitution - Missense |
c.3108T>G; p.H1036Q; 13:33106874-33106874 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2122C>T; p.H708Y; 13:33118224-33118224 |
skin | malignant_melanoma | Substitution - Missense |
c.2122C>T; p.H708Y; 13:33118224-33118224 |
liver | carcinoma | Substitution - Missense |
c.2122C>T; p.H708Y; 13:33118224-33118224 |
liver | carcinoma | Substitution - Missense |
c.380G>A; p.R127K; 13:33142317-33142317 |
skin | malignant_melanoma | Substitution - Missense |
c.285T>C; p.H95H; 13:33165375-33165375 |
breast | carcinoma | Substitution - coding silent |
c.461C>A; p.S154Y; 13:33130216-33130216 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2802G>A; p.T934T; 13:33110713-33110713 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1171G>T; p.E391*; 13:33129506-33129506 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.638G>T; p.G213V; 13:33130039-33130039 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1638G>A; p.T546T; 13:33129039-33129039 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.368T>C; p.V123A; 13:33142329-33142329 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2669_2670insA; p.T891fs*131; 13:33110845-33110846 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Insertion - Frameshift |
c.1148G>A; p.R383H; 13:33129529-33129529 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2219G>A; p.R740Q; 13:33118127-33118127 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.3011T>G; p.M1004R; 13:33109909-33109909 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.591C>A; p.S197S; 13:33130086-33130086 |
skin | malignant_melanoma | Substitution - coding silent |
c.2034A>C; p.Q678H; 13:33126129-33126129 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.2117G>A; p.R706Q; 13:33118229-33118229 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3174G>A; p.P1058P; 13:33106808-33106808 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.309A>T; p.V103V; 13:33165351-33165351 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1309C>T; p.Q437*; 13:33129368-33129368 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.309A>T; p.V103V; 13:33165351-33165351 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1957C>T; p.P653S; 13:33126206-33126206 |
skin | malignant_melanoma | Substitution - Missense |
c.1500C>T; p.V500V; 13:33129177-33129177 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2076C>T; p.L692L; 13:33126087-33126087 |
skin | malignant_melanoma | Substitution - coding silent |
c.2076C>T; p.L692L; 13:33126087-33126087 |
breast | carcinoma | Substitution - coding silent |
c.749A>G; p.K250R; 13:33129928-33129928 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.515C>T; p.P172L; 13:33130162-33130162 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.549T>C; p.S183S; 13:33130128-33130128 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.487C>A; p.L163I; 13:33130190-33130190 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1137G>A; p.G379G; 13:33129540-33129540 |
skin | malignant_melanoma | Substitution - coding silent |
c.85C>A; p.R29R; 13:33285554-33285554 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2150T>C; p.F717S; 13:33118196-33118196 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.3074G>A; p.G1025E; 13:33106908-33106908 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.493C>T; p.R165*; 13:33130184-33130184 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.1112C>T; p.A371V; 13:33129565-33129565 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.435T>C; p.T145T; 13:33130242-33130242 |
pancreas | carcinoma | Substitution - coding silent |
c.2276A>G; p.Y759C; 13:33118070-33118070 |
lung; left_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.2276A>G; p.Y759C; 13:33118070-33118070 |
liver | carcinoma | Substitution - Missense |
c.1801G>T; p.A601S; 13:33127494-33127494 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1409G>A; p.S470N; 13:33129268-33129268 |
kidney | other; neoplasm | Substitution - Missense |
c.2386G>A; p.V796I; 13:33112827-33112827 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.400G>A; p.D134N; 13:33130277-33130277 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2386G>A; p.V796I; 13:33112827-33112827 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.253C>T; p.P85S; 13:33165407-33165407 |
skin | malignant_melanoma | Substitution - Missense |
c.124A>C; p.S42R; 13:33285515-33285515 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2516C>A; p.T839N; 13:33111869-33111869 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1391G>T; p.G464V; 13:33129286-33129286 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2311G>A; p.V771M; 13:33112902-33112902 |
oesophagus | carcinoma | Substitution - Missense |
c.2299C>T; p.R767W; 13:33112914-33112914 |
breast | carcinoma | Substitution - Missense |
c.1123C>G; p.L375V; 13:33129554-33129554 |
soft_tissue; striated_muscle | rhabdoid_tumour | Substitution - Missense |
c.1637C>T; p.T546M; 13:33129040-33129040 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.708delC; p.R237fs*24; 13:33129969-33129969 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1838T>A; p.L613Q; 13:33127457-33127457 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.2505G>T; p.K835N; 13:33111880-33111880 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3180C>T; p.G1060G; 13:33106802-33106802 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1965C>T; p.Y655Y; 13:33126198-33126198 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.619G>C; p.D207H; 13:33130058-33130058 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2544C>T; p.N848N; 13:33111841-33111841 |
pancreas | carcinoma | Substitution - coding silent |
c.2178G>T; p.Q726H; 13:33118168-33118168 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2075T>C; p.L692P; 13:33126088-33126088 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3032A>T; p.D1011V; 13:33109888-33109888 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1243C>A; p.L415I; 13:33129434-33129434 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1980C>T; p.V660V; 13:33126183-33126183 |
skin | malignant_melanoma | Substitution - coding silent |
c.1243C>A; p.L415I; 13:33129434-33129434 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2131C>T; p.R711C; 13:33118215-33118215 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.420C>T; p.I140I; 13:33130257-33130257 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.670G>A; p.D224N; 13:33130007-33130007 |
skin | malignant_melanoma | Substitution - Missense |
c.288T>C; p.D96D; 13:33165372-33165372 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.619G>A; p.D207N; 13:33130058-33130058 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.505A>C; p.N169H; 13:33130172-33130172 |
skin | malignant_melanoma | Substitution - Missense |
c.2448delC; p.S817fs*8; 13:33112765-33112765 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2682A>G; p.E894E; 13:33110833-33110833 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.225C>T; p.Y75Y; 13:33167567-33167567 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1167C>T; p.S389S; 13:33129510-33129510 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.192T>C; p.C64C; 13:33167600-33167600 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1868G>A; p.R623H; 13:33127427-33127427 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2063G>A; p.R688H; 13:33126100-33126100 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1339A>G; p.M447V; 13:33129338-33129338 |
pancreas | NS | Substitution - Missense |
c.1343C>T; p.A448V; 13:33129334-33129334 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2708G>T; p.G903V; 13:33110807-33110807 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1363C>G; p.R455G; 13:33129314-33129314 |
liver | carcinoma | Substitution - Missense |
c.2306A>G; p.Q769R; 13:33112907-33112907 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1986C>T; p.G662G; 13:33126177-33126177 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2417C>T; p.T806M; 13:33112796-33112796 |
prostate | carcinoma | Substitution - Missense |
c.1363C>G; p.R455G; 13:33129314-33129314 |
liver | carcinoma | Substitution - Missense |
c.2708G>T; p.G903V; 13:33110807-33110807 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.941C>T; p.S314L; 13:33129736-33129736 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3299C>A; p.S1100Y; 13:33105636-33105636 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.941C>T; p.S314L; 13:33129736-33129736 |
skin | malignant_melanoma | Substitution - Missense |
c.2418G>A; p.T806T; 13:33112795-33112795 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3058A>G; p.T1020A; 13:33106924-33106924 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2222A>T; p.D741V; 13:33118124-33118124 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1775T>C; p.L592P; 13:33127520-33127520 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.451C>T; p.R151C; 13:33130226-33130226 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1775T>C; p.L592P; 13:33127520-33127520 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.280G>A; p.D94N; 13:33165380-33165380 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3098C>T; p.S1033F; 13:33106884-33106884 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.539C>T; p.T180M; 13:33130138-33130138 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.125G>C; p.S42T; 13:33285514-33285514 |
breast | carcinoma | Substitution - Missense |
c.2926C>T; p.L976L; 13:33109994-33109994 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.839G>A; p.R280Q; 13:33129838-33129838 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.839G>A; p.R280Q; 13:33129838-33129838 |
skin | malignant_melanoma | Substitution - Missense |
c.512C>T; p.S171L; 13:33130165-33130165 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1014C>T; p.H338H; 13:33129663-33129663 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2472G>A; p.L824L; 13:33112741-33112741 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.2472G>A; p.L824L; 13:33112741-33112741 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.2058T>C; p.Y686Y; 13:33126105-33126105 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1173G>T; p.E391D; 13:33129504-33129504 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1714T>C; p.S572P; 13:33128963-33128963 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2076C>G; p.L692L; 13:33126087-33126087 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.849C>T; p.G283G; 13:33129828-33129828 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1895C>T; p.S632F; 13:33127400-33127400 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2774T>A; p.F925Y; 13:33110741-33110741 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3067C>T; p.P1023S; 13:33106915-33106915 |
skin | malignant_melanoma | Substitution - Missense |
c.1232C>T; p.S411F; 13:33129445-33129445 |
skin | malignant_melanoma | Substitution - Missense |
c.2528A>G; p.D843G; 13:33111857-33111857 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1887G>A; p.E629E; 13:33127408-33127408 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.618C>T; p.S206S; 13:33130059-33130059 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2005G>A; p.V669I; 13:33126158-33126158 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |