General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 2903 |
Name | GRIN2A |
Synonymous | glutamate receptor, ionotropic, N-methyl D-aspartate 2A;GRIN2A;glutamate receptor, ionotropic, N-methyl D-aspartate 2A |
Definition | N-methyl D-aspartate receptor subtype 2A|N-methyl-D-aspartate receptor channel, subunit epsilon-1|N-methyl-D-aspartate receptor subunit 2A|glutamate receptor ionotropic, NMDA 2A |
Position | 16p13.2 |
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 0.08. |
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.3909C>T; p.D1303D; 16:9763635-9763635 |
skin | malignant_melanoma | Substitution - coding silent |
c.1231C>A; p.L411M; 16:9849853-9849853 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3026G>A; p.R1009K; 16:9764518-9764518 |
skin | malignant_melanoma | Substitution - Missense |
c.3952C>T; p.R1318W; 16:9763592-9763592 |
skin | malignant_melanoma | Substitution - Missense |
c.3765G>A; p.Q1255Q; 16:9763779-9763779 |
skin | malignant_melanoma | Substitution - coding silent |
c.2167G>T; p.G723W; 16:9822265-9822265 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3051C>T; p.S1017S; 16:9764493-9764493 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3786C>A; p.T1262T; 16:9763758-9763758 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.2759G>A; p.R920K; 16:9764785-9764785 |
NS | malignant_melanoma | Substitution - Missense |
c.3566A>T; p.K1189M; 16:9763978-9763978 |
oesophagus | carcinoma | Substitution - Missense |
c.904G>A; p.A302T; 16:9938062-9938062 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.904G>A; p.A302T; 16:9938062-9938062 |
pancreas | carcinoma; ductal_carcinoma | Substitution - Missense |
c.3744C>T; p.I1248I; 16:9763800-9763800 |
skin | malignant_melanoma | Substitution - coding silent |
c.3827C>T; p.A1276V; 16:9763717-9763717 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.904G>A; p.A302T; 16:9938062-9938062 |
pancreas | carcinoma | Substitution - Missense |
c.904G>A; p.A302T; 16:9938062-9938062 |
stomach | adenocarcinoma | Substitution - Missense |
c.3135C>T; p.S1045S; 16:9764409-9764409 |
skin | malignant_melanoma | Substitution - coding silent |
c.2535G>T; p.L845L; 16:9768911-9768911 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.3744C>T; p.I1248I; 16:9763800-9763800 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2499C>T; p.I833I; 16:9768947-9768947 |
skin | malignant_melanoma | Substitution - coding silent |
c.3890A>T; p.D1297V; 16:9763654-9763654 |
pancreas | carcinoma | Substitution - Missense |
c.1251C>T; p.V417V; 16:9849833-9849833 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3920C>T; p.P1307L; 16:9763624-9763624 |
skin | malignant_melanoma | Substitution - Missense |
c.2499C>T; p.I833I; 16:9768947-9768947 |
skin | malignant_melanoma | Substitution - coding silent |
c.2195C>T; p.A732V; 16:9798438-9798438 |
skin; arm | malignant_melanoma | Substitution - Missense |
c.3744C>A; p.I1248I; 16:9763800-9763800 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2857G>C; p.E953Q; 16:9764687-9764687 |
skin | malignant_melanoma | Substitution - Missense |
c.2550G>A; p.T850T; 16:9768896-9768896 |
prostate | carcinoma | Substitution - coding silent |
c.3281A>G; p.Y1094C; 16:9764263-9764263 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2302G>T; p.G768C; 16:9798331-9798331 |
bone | osteosarcoma | Substitution - Missense |
c.2550G>A; p.T850T; 16:9768896-9768896 |
breast | carcinoma | Substitution - coding silent |
c.2550G>A; p.T850T; 16:9768896-9768896 |
skin | malignant_melanoma | Substitution - coding silent |
c.487_488CA>AG; p.Q163R; 16:9938478-9938479 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3993C>A; p.V1331V; 16:9763551-9763551 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.3616C>T; p.R1206*; 16:9763928-9763928 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.3070G>A; p.D1024N; 16:9764474-9764474 |
skin | malignant_melanoma | Substitution - Missense |
c.3616C>T; p.R1206*; 16:9763928-9763928 |
ovary | carcinoma; serous_carcinoma | Substitution - Nonsense |
c.2416G>A; p.E806K; 16:9769030-9769030 |
skin | malignant_melanoma | Substitution - Missense |
c.2326G>T; p.D776Y; 16:9798307-9798307 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2416G>A; p.E806K; 16:9769030-9769030 |
skin | malignant_melanoma | Substitution - Missense |
c.3616C>T; p.R1206*; 16:9763928-9763928 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.2416G>A; p.E806K; 16:9769030-9769030 |
skin | malignant_melanoma | Substitution - Missense |
c.4215G>A; p.L1405L; 16:9763329-9763329 |
skin | malignant_melanoma | Substitution - coding silent |
c.3596C>A; p.P1199Q; 16:9763948-9763948 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.2533C>G; p.L845V; 16:9768913-9768913 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3102G>A; p.R1034R; 16:9764442-9764442 |
skin | malignant_melanoma | Substitution - coding silent |
c.1164C>T; p.A388A; 16:9849920-9849920 |
prostate | carcinoma | Substitution - coding silent |
c.3102G>A; p.R1034R; 16:9764442-9764442 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.262G>A; p.D88N; 16:10180150-10180150 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1022T>C; p.V341A; 16:9891086-9891086 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2178C>T; p.D726D; 16:9798455-9798455 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2962C>A; p.L988I; 16:9764582-9764582 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1577T>C; p.V526A; 16:9840721-9840721 |
breast | carcinoma | Substitution - Missense |
c.588G>T; p.V196V; 16:9938378-9938378 |
skin | malignant_melanoma | Substitution - coding silent |
c.987C>T; p.V329V; 16:9937979-9937979 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2786C>T; p.S929F; 16:9764758-9764758 |
skin; mucosal | malignant_melanoma; acral_lentiginous | Substitution - Missense |
c.20G>A; p.W7*; 16:10180392-10180392 |
skin; neck | malignant_melanoma | Substitution - Nonsense |
c.2786C>T; p.S929F; 16:9764758-9764758 |
skin; trunk | malignant_melanoma; nodular | Substitution - Missense |
c.81G>A; p.A27A; 16:10180331-10180331 |
skin | malignant_melanoma | Substitution - coding silent |
c.1468A>T; p.N490Y; 16:9840965-9840965 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.150A>G; p.E50E; 16:10180262-10180262 |
skin | malignant_melanoma | Substitution - coding silent |
c.1126G>A; p.G376S; 16:9849958-9849958 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3221C>T; p.P1074L; 16:9764323-9764323 |
skin; upper_back | malignant_melanoma | Substitution - Missense |
c.3604G>A; p.E1202K; 16:9763940-9763940 |
skin | malignant_melanoma | Substitution - Missense |
c.3987T>G; p.F1329L; 16:9763557-9763557 |
skin | malignant_melanoma | Substitution - Missense |
c.4185G>A; p.A1395A; 16:9763359-9763359 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3333C>G; p.S1111R; 16:9764211-9764211 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.2902G>C; p.A968P; 16:9764642-9764642 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1213C>A; p.H405N; 16:9849871-9849871 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3336C>A; p.S1112S; 16:9764208-9764208 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2748C>A; p.D916E; 16:9764796-9764796 |
adrenal_gland; adrenal_gland | adrenal_cortical_carcinoma; functioning | Substitution - Missense |
c.3007G>T; p.E1003*; 16:9764537-9764537 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.3361G>C; p.D1121H; 16:9764183-9764183 |
breast | carcinoma | Substitution - Missense |
c.2326G>A; p.D776N; 16:9798307-9798307 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1690A>T; p.M564L; 16:9834192-9834192 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.3206C>T; p.T1069M; 16:9764338-9764338 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3506G>A; p.R1169Q; 16:9764038-9764038 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3206C>T; p.T1069M; 16:9764338-9764338 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.3506G>A; p.R1169Q; 16:9764038-9764038 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.3206C>T; p.T1069M; 16:9764338-9764338 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2135G>A; p.G712E; 16:9822297-9822297 |
skin; shoulder | malignant_melanoma | Substitution - Missense |
c.3709G>A; p.D1237N; 16:9763835-9763835 |
skin | malignant_melanoma | Substitution - Missense |
c.3506G>A; p.R1169Q; 16:9764038-9764038 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3169G>A; p.A1057T; 16:9764375-9764375 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3709G>A; p.D1237N; 16:9763835-9763835 |
skin; trunk | malignant_melanoma; nodular | Substitution - Missense |
c.2135G>A; p.G712E; 16:9822297-9822297 |
skin | malignant_melanoma | Substitution - Missense |
c.3506G>A; p.R1169Q; 16:9764038-9764038 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2053G>C; p.V685L; 16:9822379-9822379 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.3667A>T; p.T1223S; 16:9763877-9763877 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.3011C>A; p.S1004Y; 16:9764533-9764533 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3889G>A; p.D1297N; 16:9763655-9763655 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.1514C>A; p.A505E; 16:9840784-9840784 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.3033G>A; p.R1011R; 16:9764511-9764511 |
prostate | carcinoma | Substitution - coding silent |
c.1314G>A; p.K438K; 16:9849770-9849770 |
ovary | other; neoplasm | Substitution - coding silent |
c.2828A>G; p.Y943C; 16:9764716-9764716 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3074C>T; p.S1025L; 16:9764470-9764470 |
NS | malignant_melanoma | Substitution - Missense |
c.3074C>T; p.S1025L; 16:9764470-9764470 |
skin | malignant_melanoma | Substitution - Missense |
c.864G>A; p.L288L; 16:9938102-9938102 |
skin | malignant_melanoma | Substitution - coding silent |
c.1928C>G; p.A643G; 16:9829502-9829502 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.2695C>T; p.R899W; 16:9764849-9764849 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2412G>T; p.K804N; 16:9769034-9769034 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2901G>A; p.V967V; 16:9764643-9764643 |
skin | malignant_melanoma | Substitution - coding silent |
c.1510C>T; p.R504W; 16:9840788-9840788 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1510C>T; p.R504W; 16:9840788-9840788 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2041C>T; p.R681*; 16:9822391-9822391 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2041C>T; p.R681*; 16:9822391-9822391 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1702G>T; p.V568F; 16:9834180-9834180 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1959G>A; p.M653I; 16:9829471-9829471 |
NS | malignant_melanoma | Substitution - Missense |
c.1959G>A; p.M653I; 16:9829471-9829471 |
skin | malignant_melanoma | Substitution - Missense |
c.2232C>T; p.G744G; 16:9798401-9798401 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1213C>G; p.H405D; 16:9849871-9849871 |
breast | carcinoma; ductal_carcinoma | Substitution - Missense |
c.3965G>A; p.G1322E; 16:9763579-9763579 |
skin | malignant_melanoma | Substitution - Missense |
c.4298C>T; p.A1433V; 16:9763246-9763246 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2973C>T; p.S991S; 16:9764571-9764571 |
skin | malignant_melanoma | Substitution - coding silent |
c.1959G>A; p.M653I; 16:9829471-9829471 |
skin; ear | malignant_melanoma | Substitution - Missense |
c.3965G>A; p.G1322E; 16:9763579-9763579 |
skin | malignant_melanoma | Substitution - Missense |
c.3965G>A; p.G1322E; 16:9763579-9763579 |
skin | malignant_melanoma | Substitution - Missense |
c.3965G>A; p.G1322E; 16:9763579-9763579 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3394C>T; p.P1132S; 16:9764150-9764150 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.3394C>T; p.P1132S; 16:9764150-9764150 |
skin | malignant_melanoma | Substitution - Missense |
c.4058G>A; p.R1353K; 16:9763486-9763486 |
skin | malignant_melanoma | Substitution - Missense |
c.4027C>A; p.L1343I; 16:9763517-9763517 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.202A>C; p.N68H; 16:10180210-10180210 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3849G>C; p.K1283N; 16:9763695-9763695 |
thyroid | other; neoplasm | Substitution - Missense |
c.57C>T; p.R19R; 16:10180355-10180355 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.1366T>A; p.C456S; 16:9841067-9841067 |
oesophagus | carcinoma | Substitution - Missense |
c.1757G>T; p.R586I; 16:9834125-9834125 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.96delC; p.A33fs*2; 16:10180316-10180316 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.718C>T; p.L240L; 16:9938248-9938248 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - coding silent |
c.3857T>G; p.I1286S; 16:9763687-9763687 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.39G>A; p.P13P; 16:10180373-10180373 |
liver | carcinoma | Substitution - coding silent |
c.1113A>T; p.E371D; 16:9890995-9890995 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1593G>A; p.T531T; 16:9840705-9840705 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.3879T>C; p.D1293D; 16:9763665-9763665 |
skin | malignant_melanoma | Substitution - coding silent |
c.4161C>A; p.Y1387*; 16:9763383-9763383 |
autonomic_ganglia | neuroblastoma | Substitution - Nonsense |
c.3687C>A; p.T1229T; 16:9763857-9763857 |
oesophagus | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.3157C>G; p.P1053A; 16:9764387-9764387 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.1317C>T; p.F439F; 16:9849767-9849767 |
skin | malignant_melanoma | Substitution - coding silent |
c.97G>A; p.A33T; 16:10180315-10180315 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1202C>A; p.P401Q; 16:9849882-9849882 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1980C>G; p.D660E; 16:9829450-9829450 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.945G>T; p.E315D; 16:9938021-9938021 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3975C>T; p.Y1325Y; 16:9763569-9763569 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.97G>A; p.A33T; 16:10180315-10180315 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3975C>T; p.Y1325Y; 16:9763569-9763569 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1438G>T; p.V480L; 16:9840995-9840995 |
kidney | carcinoma; renal_cell_carcinoma | Substitution - Missense |
c.1317C>T; p.F439F; 16:9849767-9849767 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1317C>T; p.F439F; 16:9849767-9849767 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1317C>T; p.F439F; 16:9849767-9849767 |
skin | malignant_melanoma | Substitution - coding silent |
c.3347A>G; p.K1116R; 16:9764197-9764197 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.3379G>T; p.G1127C; 16:9764165-9764165 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.609G>A; p.V203V; 16:9938357-9938357 |
skin | malignant_melanoma | Substitution - coding silent |
c.4032C>T; p.F1344F; 16:9763512-9763512 |
skin | malignant_melanoma | Substitution - coding silent |
c.1151G>T; p.S384I; 16:9849933-9849933 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.609G>A; p.V203V; 16:9938357-9938357 |
skin | malignant_melanoma | Substitution - coding silent |
c.4261G>A; p.D1421N; 16:9763283-9763283 |
skin; neck | malignant_melanoma | Substitution - Missense |
c.2180C>T; p.A727V; 16:9798453-9798453 |
skin | malignant_melanoma | Substitution - Missense |
c.3011C>G; p.S1004C; 16:9764533-9764533 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.4202T>G; p.L1401R; 16:9763342-9763342 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1529G>A; p.G510D; 16:9840769-9840769 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1403C>T; p.S468F; 16:9841030-9841030 |
skin | malignant_melanoma | Substitution - Missense |
c.3433G>A; p.V1145M; 16:9764111-9764111 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1491C>A; p.I497I; 16:9840942-9840942 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1407_1408insT; p.T470fs*21; 16:9841025-9841026 |
breast | carcinoma | Insertion - Frameshift |
c.3372G>T; p.K1124N; 16:9764172-9764172 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.273C>T; p.S91S; 16:10180139-10180139 |
skin | malignant_melanoma | Substitution - coding silent |
c.4385C>G; p.S1462C; 16:9763159-9763159 |
large_intestine; rectum | malignant_melanoma | Substitution - Missense |
c.2512G>A; p.E838K; 16:9768934-9768934 |
skin | malignant_melanoma | Substitution - Missense |
c.995A>G; p.H332R; 16:9937971-9937971 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3867G>T; p.Q1289H; 16:9763677-9763677 |
skin | malignant_melanoma | Substitution - Missense |
c.3028C>A; p.P1010T; 16:9764516-9764516 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1204G>A; p.D402N; 16:9849880-9849880 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3939C>T; p.L1313L; 16:9763605-9763605 |
skin | malignant_melanoma | Substitution - coding silent |
c.666C>A; p.I222I; 16:9938300-9938300 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2277C>A; p.T759T; 16:9798356-9798356 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3303C>T; p.V1101V; 16:9764241-9764241 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3303C>T; p.V1101V; 16:9764241-9764241 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2809G>A; p.D937N; 16:9764735-9764735 |
skin | malignant_melanoma | Substitution - Missense |
c.2775C>T; p.I925I; 16:9764769-9764769 |
skin | malignant_melanoma | Substitution - coding silent |
c.549C>T; p.F183F; 16:9938417-9938417 |
skin | malignant_melanoma | Substitution - coding silent |
c.2972C>T; p.S991F; 16:9764572-9764572 |
skin | malignant_melanoma | Substitution - Missense |
c.3681C>T; p.H1227H; 16:9763863-9763863 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1595G>A; p.G532E; 16:9840703-9840703 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1927G>A; p.A643T; 16:9829503-9829503 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.652C>A; p.Q218K; 16:9938314-9938314 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2302G>A; p.G768S; 16:9798331-9798331 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1774A>G; p.K592E; 16:9834108-9834108 |
skin; foot | malignant_melanoma; acral_lentiginous | Substitution - Missense |
c.75G>A; p.A25A; 16:10180337-10180337 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3511C>T; p.P1171S; 16:9764033-9764033 |
skin | malignant_melanoma | Substitution - Missense |
c.1030G>A; p.D344N; 16:9891078-9891078 |
skin | malignant_melanoma | Substitution - Missense |
c.1752C>A; p.Y584*; 16:9834130-9834130 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.1030G>A; p.D344N; 16:9891078-9891078 |
skin | malignant_melanoma | Substitution - Missense |
c.1141C>T; p.H381Y; 16:9849943-9849943 |
skin | malignant_melanoma | Substitution - Missense |
c.3735C>A; p.L1245L; 16:9763809-9763809 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3854G>A; p.R1285K; 16:9763690-9763690 |
skin; arm | malignant_melanoma | Substitution - Missense |
c.940C>T; p.P314S; 16:9938026-9938026 |
skin | malignant_melanoma | Substitution - Missense |
c.3240C>T; p.H1080H; 16:9764304-9764304 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4181A>T; p.Q1394L; 16:9763363-9763363 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2057C>T; p.P686L; 16:9822375-9822375 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.3045G>A; p.K1015K; 16:9764499-9764499 |
skin | malignant_melanoma | Substitution - coding silent |
c.3045G>A; p.K1015K; 16:9764499-9764499 |
skin | malignant_melanoma | Substitution - coding silent |
c.3424C>A; p.P1142T; 16:9764120-9764120 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.4170G>A; p.S1390S; 16:9763374-9763374 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4170G>A; p.S1390S; 16:9763374-9763374 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.87G>A; p.K29K; 16:10180325-10180325 |
skin | malignant_melanoma | Substitution - coding silent |
c.4101C>T; p.F1367F; 16:9763443-9763443 |
skin | malignant_melanoma | Substitution - coding silent |
c.2563G>C; p.D855H; 16:9768883-9768883 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.4204C>T; p.R1402W; 16:9763340-9763340 |
skin | malignant_melanoma | Substitution - Missense |
c.1207G>A; p.D403N; 16:9849877-9849877 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.423G>T; p.T141T; 16:9938543-9938543 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; Burkitt_lymphoma | Substitution - coding silent |
c.3572T>C; p.F1191S; 16:9763972-9763972 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1667C>T; p.S556F; 16:9834215-9834215 |
skin | malignant_melanoma | Substitution - Missense |
c.3572T>C; p.F1191S; 16:9763972-9763972 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4204C>T; p.R1402W; 16:9763340-9763340 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.658A>G; p.K220E; 16:9938308-9938308 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.91C>T; p.P31S; 16:10180321-10180321 |
skin | malignant_melanoma | Substitution - Missense |
c.3457G>A; p.D1153N; 16:9764087-9764087 |
skin; scalp | malignant_melanoma | Substitution - Missense |
c.658A>G; p.K220E; 16:9938308-9938308 |
liver | carcinoma | Substitution - Missense |
c.3457G>A; p.D1153N; 16:9764087-9764087 |
skin | malignant_melanoma | Substitution - Missense |
c.658A>G; p.K220E; 16:9938308-9938308 |
liver | carcinoma | Substitution - Missense |
c.814T>C; p.F272L; 16:9938152-9938152 |
pancreas | carcinoma | Substitution - Missense |
c.1794T>C; p.S598S; 16:9829636-9829636 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1111G>A; p.E371K; 16:9890997-9890997 |
skin; upper_back | malignant_melanoma | Substitution - Missense |
c.2179G>A; p.A727T; 16:9798454-9798454 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3215G>A; p.R1072K; 16:9764329-9764329 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1111G>A; p.E371K; 16:9890997-9890997 |
skin; trunk | malignant_melanoma; nodular | Substitution - Missense |
c.3442C>T; p.P1148S; 16:9764102-9764102 |
skin | malignant_melanoma | Substitution - Missense |
c.1111G>A; p.E371K; 16:9890997-9890997 |
skin; arm | malignant_melanoma | Substitution - Missense |
c.235C>T; p.P79S; 16:10180177-10180177 |
skin | malignant_melanoma | Substitution - Missense |
c.1135G>A; p.E379K; 16:9849949-9849949 |
skin | malignant_melanoma | Substitution - Missense |
c.1037A>C; p.K346T; 16:9891071-9891071 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.890G>T; p.G297V; 16:9938076-9938076 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1980C>A; p.D660E; 16:9829450-9829450 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3677G>A; p.G1226D; 16:9763867-9763867 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3065G>A; p.R1022H; 16:9764479-9764479 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3169G>T; p.A1057S; 16:9764375-9764375 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.3065G>A; p.R1022H; 16:9764479-9764479 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.4274C>T; p.S1425L; 16:9763270-9763270 |
skin | malignant_melanoma | Substitution - Missense |
c.1831C>T; p.L611L; 16:9829599-9829599 |
skin | malignant_melanoma | Substitution - coding silent |
c.4274C>T; p.S1425L; 16:9763270-9763270 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.4274C>T; p.S1425L; 16:9763270-9763270 |
skin; face | malignant_melanoma | Substitution - Missense |
c.1747G>A; p.G583R; 16:9834135-9834135 |
skin | malignant_melanoma | Substitution - Missense |
c.350C>T; p.S117F; 16:10180062-10180062 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.2746G>A; p.D916N; 16:9764798-9764798 |
skin | malignant_melanoma | Substitution - Missense |
c.1110G>A; p.R370R; 16:9890998-9890998 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2161A>C; p.K721Q; 16:9822271-9822271 |
skin | malignant_melanoma | Substitution - Missense |
c.871A>G; p.R291G; 16:9938095-9938095 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.4230G>A; p.S1410S; 16:9763314-9763314 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.1425C>T; p.Y475Y; 16:9841008-9841008 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2917G>T; p.D973Y; 16:9764627-9764627 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1425C>T; p.Y475Y; 16:9841008-9841008 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1214A>G; p.H405R; 16:9849870-9849870 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1425C>T; p.Y475Y; 16:9841008-9841008 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2559C>T; p.C853C; 16:9768887-9768887 |
skin | malignant_melanoma | Substitution - coding silent |
c.3341G>C; p.R1114T; 16:9764203-9764203 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.3341G>C; p.R1114T; 16:9764203-9764203 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.136G>T; p.V46L; 16:10180276-10180276 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1451A>T; p.K484M; 16:9840982-9840982 |
skin | malignant_melanoma | Substitution - Missense |
c.3356C>A; p.T1119N; 16:9764188-9764188 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1029G>A; p.W343*; 16:9891079-9891079 |
skin; back | malignant_melanoma | Substitution - Nonsense |
c.1417T>A; p.F473I; 16:9841016-9841016 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1534C>T; p.L512F; 16:9840764-9840764 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.3298G>A; p.E1100K; 16:9764246-9764246 |
oesophagus | carcinoma | Substitution - Missense |
c.1114T>C; p.W372R; 16:9890994-9890994 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2357-9T>A; p.?; 16:9769098-9769098 |
soft_tissue; striated_muscle | rhabdomyosarcoma; embryonal | Unknown |
c.1570T>G; p.F524V; 16:9840728-9840728 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2111A>G; p.Y704C; 16:9822321-9822321 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2547C>A; p.F849L; 16:9768899-9768899 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.3616C>A; p.R1206R; 16:9763928-9763928 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3616C>A; p.R1206R; 16:9763928-9763928 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3309C>A; p.R1103R; 16:9764235-9764235 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4096C>T; p.P1366S; 16:9763448-9763448 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.3543C>T; p.N1181N; 16:9764001-9764001 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3491C>T; p.T1164M; 16:9764053-9764053 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3543C>T; p.N1181N; 16:9764001-9764001 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3491C>T; p.T1164M; 16:9764053-9764053 |
bone; femur | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.3255_3261delCTTTAAA; p.N1085fs*20; 16:9764283-9764289 |
breast | carcinoma | Deletion - Frameshift |
c.3152A>G; p.Y1051C; 16:9764392-9764392 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.390C>T; p.G130G; 16:10180022-10180022 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.4126C>A; p.R1376S; 16:9763418-9763418 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1203G>T; p.P401P; 16:9849881-9849881 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.170C>A; p.P57H; 16:10180242-10180242 |
skin | malignant_melanoma | Substitution - Missense |
c.1248C>T; p.F416F; 16:9849836-9849836 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.199G>A; p.V67M; 16:10180213-10180213 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; polycythaemia_vera | Substitution - Missense |
c.547T>A; p.F183I; 16:9938419-9938419 |
NS | malignant_melanoma | Substitution - Missense |
c.3582A>G; p.K1194K; 16:9763962-9763962 |
bone; humerus | other; chondroblastoma | Substitution - coding silent |
c.3617G>A; p.R1206Q; 16:9763927-9763927 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.382C>G; p.H128D; 16:10180030-10180030 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.2253G>A; p.G751G; 16:9798380-9798380 |
skin | malignant_melanoma | Substitution - coding silent |
c.3444G>A; p.P1148P; 16:9764100-9764100 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2227G>A; p.E743K; 16:9798406-9798406 |
skin | malignant_melanoma | Substitution - Missense |
c.144G>A; p.E48E; 16:10180268-10180268 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1996A>G; p.S666G; 16:9829434-9829434 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1249G>A; p.V417I; 16:9849835-9849835 |
breast | carcinoma | Substitution - Missense |
c.3924C>T; p.S1308S; 16:9763620-9763620 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - coding silent |
c.3722G>A; p.R1241Q; 16:9763822-9763822 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1249G>A; p.V417I; 16:9849835-9849835 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.3722G>A; p.R1241Q; 16:9763822-9763822 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1900T>A; p.W634R; 16:9829530-9829530 |
skin | malignant_melanoma | Substitution - Missense |
c.3901G>A; p.E1301K; 16:9763643-9763643 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.329C>A; p.A110D; 16:10180083-10180083 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2458G>A; p.V820I; 16:9768988-9768988 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.2884G>A; p.E962K; 16:9764660-9764660 |
skin; chest | malignant_melanoma | Substitution - Missense |
c.2884G>A; p.E962K; 16:9764660-9764660 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2884G>A; p.E962K; 16:9764660-9764660 |
meninges | meningioma; secretory | Substitution - Missense |
c.2884G>A; p.E962K; 16:9764660-9764660 |
skin | malignant_melanoma | Substitution - Missense |
c.1585G>T; p.V529L; 16:9840713-9840713 |
breast | carcinoma | Substitution - Missense |
c.1680G>A; p.M560I; 16:9834202-9834202 |
skin | malignant_melanoma | Substitution - Missense |
c.2018C>A; p.P673H; 16:9822414-9822414 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1693C>A; p.L565M; 16:9834189-9834189 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2884G>A; p.E962K; 16:9764660-9764660 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2553C>T; p.G851G; 16:9768893-9768893 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2912A>G; p.Q971R; 16:9764632-9764632 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.1028G>A; p.W343*; 16:9891080-9891080 |
skin; extremity | malignant_melanoma | Substitution - Nonsense |
c.3373G>T; p.E1125*; 16:9764171-9764171 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2884G>A; p.E962K; 16:9764660-9764660 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2458G>A; p.V820I; 16:9768988-9768988 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.2884G>A; p.E962K; 16:9764660-9764660 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3537C>T; p.S1179S; 16:9764007-9764007 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2140G>C; p.E714Q; 16:9822292-9822292 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.2884G>A; p.E962K; 16:9764660-9764660 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.2996C>T; p.A999V; 16:9764548-9764548 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3348G>T; p.K1116N; 16:9764196-9764196 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3109G>A; p.A1037T; 16:9764435-9764435 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2975A>C; p.N992T; 16:9764569-9764569 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.4089C>T; p.S1363S; 16:9763455-9763455 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2755A>G; p.K919E; 16:9764789-9764789 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.172G>A; p.E58K; 16:10180240-10180240 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4380C>T; p.I1460I; 16:9763164-9763164 |
skin | malignant_melanoma | Substitution - coding silent |
c.4380C>T; p.I1460I; 16:9763164-9763164 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1828G>A; p.G610S; 16:9829602-9829602 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3505C>A; p.R1169R; 16:9764039-9764039 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2095C>T; p.P699S; 16:9822337-9822337 |
skin | malignant_melanoma | Substitution - Missense |
c.2095C>T; p.P699S; 16:9822337-9822337 |
skin | malignant_melanoma | Substitution - Missense |
c.2095C>T; p.P699S; 16:9822337-9822337 |
skin | malignant_melanoma | Substitution - Missense |
c.2095C>T; p.P699S; 16:9822337-9822337 |
skin | malignant_melanoma | Substitution - Missense |
c.4231T>G; p.Y1411D; 16:9763313-9763313 |
skin | malignant_melanoma | Substitution - Missense |
c.1202C>T; p.P401L; 16:9849882-9849882 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.3385C>T; p.H1129Y; 16:9764159-9764159 |
skin | malignant_melanoma | Substitution - Missense |
c.1202C>T; p.P401L; 16:9849882-9849882 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.3385C>T; p.H1129Y; 16:9764159-9764159 |
skin | malignant_melanoma | Substitution - Missense |
c.818C>T; p.P273L; 16:9938148-9938148 |
skin | malignant_melanoma | Substitution - Missense |
c.1202C>T; p.P401L; 16:9849882-9849882 |
skin | malignant_melanoma | Substitution - Missense |
c.55C>A; p.R19S; 16:10180357-10180357 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.768T>C; p.I256I; 16:9938198-9938198 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2666G>A; p.G889E; 16:9764878-9764878 |
skin; chest | malignant_melanoma | Substitution - Missense |
c.180G>A; p.A60A; 16:10180232-10180232 |
skin | malignant_melanoma | Substitution - coding silent |
c.3523G>A; p.E1175K; 16:9764021-9764021 |
skin | malignant_melanoma | Substitution - Missense |
c.1420A>G; p.T474A; 16:9841013-9841013 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.716T>C; p.I239T; 16:9938250-9938250 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3474C>T; p.F1158F; 16:9764070-9764070 |
skin | malignant_melanoma | Substitution - coding silent |
c.510C>G; p.F170L; 16:9938456-9938456 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3523G>A; p.E1175K; 16:9764021-9764021 |
breast | carcinoma | Substitution - Missense |
c.2223G>T; p.R741S; 16:9798410-9798410 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.3523G>A; p.E1175K; 16:9764021-9764021 |
skin | malignant_melanoma | Substitution - Missense |
c.3523G>A; p.E1175K; 16:9764021-9764021 |
skin; upper_back | malignant_melanoma | Substitution - Missense |
c.147C>T; p.R49R; 16:10180265-10180265 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1462A>T; p.K488*; 16:9840971-9840971 |
skin | malignant_melanoma | Substitution - Nonsense |
c.3868C>A; p.H1290N; 16:9763676-9763676 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - Missense |
c.1039G>T; p.D347Y; 16:9891069-9891069 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1183T>A; p.S395T; 16:9849901-9849901 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1084G>T; p.V362L; 16:9891024-9891024 |
liver | carcinoma | Substitution - Missense |
c.510C>T; p.F170F; 16:9938456-9938456 |
skin | malignant_melanoma | Substitution - coding silent |
c.1084G>T; p.V362L; 16:9891024-9891024 |
liver | carcinoma | Substitution - Missense |
c.1134G>A; p.W378*; 16:9849950-9849950 |
skin; knee | malignant_melanoma | Substitution - Nonsense |
c.963C>T; p.Y321Y; 16:9938003-9938003 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3052G>A; p.V1018M; 16:9764492-9764492 |
prostate | carcinoma | Substitution - Missense |
c.963C>T; p.Y321Y; 16:9938003-9938003 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1912G>A; p.A638T; 16:9829518-9829518 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.316C>T; p.Q106*; 16:10180096-10180096 |
skin | malignant_melanoma | Substitution - Nonsense |
c.3903G>A; p.E1301E; 16:9763641-9763641 |
skin | malignant_melanoma | Substitution - coding silent |
c.1912G>A; p.A638T; 16:9829518-9829518 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2387T>A; p.L796H; 16:9769059-9769059 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.3192G>A; p.T1064T; 16:9764352-9764352 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3192G>A; p.T1064T; 16:9764352-9764352 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3476G>A; p.R1159H; 16:9764068-9764068 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3476G>A; p.R1159H; 16:9764068-9764068 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.4152G>A; p.S1384S; 16:9763392-9763392 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - coding silent |
c.3646A>G; p.S1216G; 16:9763898-9763898 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2276C>A; p.T759N; 16:9798357-9798357 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3827C>G; p.A1276G; 16:9763717-9763717 |
skin; chest | malignant_melanoma | Substitution - Missense |
c.3571T>A; p.F1191I; 16:9763973-9763973 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.903C>T; p.T301T; 16:9938063-9938063 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.4249C>T; p.R1417W; 16:9763295-9763295 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2816G>T; p.G939V; 16:9764728-9764728 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3219A>G; p.E1073E; 16:9764325-9764325 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3484G>A; p.D1162N; 16:9764060-9764060 |
skin | malignant_melanoma | Substitution - Missense |
c.415G>A; p.D139N; 16:9938551-9938551 |
skin | malignant_melanoma | Substitution - Missense |
c.3080C>T; p.S1027F; 16:9764464-9764464 |
skin | malignant_melanoma | Substitution - Missense |
c.3529G>A; p.G1177R; 16:9764015-9764015 |
upper_aerodigestive_tract; pharynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1275G>A; p.L425L; 16:9849809-9849809 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.415G>A; p.D139N; 16:9938551-9938551 |
skin | malignant_melanoma | Substitution - Missense |
c.2218G>A; p.G740R; 16:9798415-9798415 |
NS | malignant_melanoma | Substitution - Missense |
c.3943G>A; p.D1315N; 16:9763601-9763601 |
skin | malignant_melanoma | Substitution - Missense |
c.3050C>T; p.S1017F; 16:9764494-9764494 |
skin | malignant_melanoma | Substitution - Missense |
c.3943G>A; p.D1315N; 16:9763601-9763601 |
skin | malignant_melanoma | Substitution - Missense |
c.1449G>A; p.G483G; 16:9840984-9840984 |
skin | malignant_melanoma | Substitution - coding silent |
c.4385C>T; p.S1462F; 16:9763159-9763159 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.372delC; p.L125fs*9; 16:10180040-10180040 |
lung | carcinoma; small_cell_carcinoma | Deletion - Frameshift |
c.2772C>T; p.F924F; 16:9764772-9764772 |
skin | malignant_melanoma | Substitution - coding silent |
c.3030_3031CC>TT; p.R1011W; 16:9764513-9764514 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2668T>C; p.S890P; 16:9764876-9764876 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1240G>A; p.A414T; 16:9849844-9849844 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.3789G>A; p.G1263G; 16:9763755-9763755 |
skin | malignant_melanoma | Substitution - coding silent |
c.2083C>T; p.R695W; 16:9822349-9822349 |
skin | malignant_melanoma | Substitution - Missense |
c.1240G>A; p.A414T; 16:9849844-9849844 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1818G>A; p.W606*; 16:9829612-9829612 |
breast | carcinoma | Substitution - Nonsense |
c.3154C>A; p.L1052I; 16:9764390-9764390 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1161C>T; p.H387H; 16:9849923-9849923 |
prostate | carcinoma | Substitution - coding silent |
c.3863G>A; p.R1288H; 16:9763681-9763681 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4381G>A; p.E1461K; 16:9763163-9763163 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3863G>A; p.R1288H; 16:9763681-9763681 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3787G>A; p.G1263R; 16:9763757-9763757 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.3863G>A; p.R1288H; 16:9763681-9763681 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.2964C>T; p.L988L; 16:9764580-9764580 |
liver | carcinoma | Substitution - coding silent |
c.2563G>A; p.D855N; 16:9768883-9768883 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1667C>A; p.S556Y; 16:9834215-9834215 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2964C>T; p.L988L; 16:9764580-9764580 |
liver | carcinoma | Substitution - coding silent |
c.3591T>G; p.G1197G; 16:9763953-9763953 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1570T>C; p.F524L; 16:9840728-9840728 |
pancreas | carcinoma | Substitution - Missense |
c.1570T>C; p.F524L; 16:9840728-9840728 |
pancreas | carcinoma | Substitution - Missense |
c.3000G>A; p.V1000V; 16:9764544-9764544 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1138A>G; p.N380D; 16:9849946-9849946 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1570T>C; p.F524L; 16:9840728-9840728 |
pancreas | carcinoma | Substitution - Missense |
c.1346G>A; p.G449E; 16:9841087-9841087 |
skin; upper_arm | malignant_melanoma | Substitution - Missense |
c.1289T>C; p.V430A; 16:9849795-9849795 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3850C>A; p.L1284I; 16:9763694-9763694 |
thyroid | other; neoplasm | Substitution - Missense |
c.468G>A; p.T156T; 16:9938498-9938498 |
skin | malignant_melanoma | Substitution - coding silent |
c.468G>A; p.T156T; 16:9938498-9938498 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3595C>G; p.P1199A; 16:9763949-9763949 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.2954C>T; p.P985L; 16:9764590-9764590 |
haematopoietic_and_lymphoid_tissue; stomach | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.3217G>A; p.E1073K; 16:9764327-9764327 |
skin | malignant_melanoma | Substitution - Missense |
c.135C>T; p.D45D; 16:10180277-10180277 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.832T>C; p.S278P; 16:9938134-9938134 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3217G>A; p.E1073K; 16:9764327-9764327 |
NS | malignant_melanoma | Substitution - Missense |
c.3217G>A; p.E1073K; 16:9764327-9764327 |
skin; ear | malignant_melanoma | Substitution - Missense |
c.1981C>A; p.Q661K; 16:9829449-9829449 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1145C>T; p.T382M; 16:9849939-9849939 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2537G>A; p.R846H; 16:9768909-9768909 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3475C>T; p.R1159C; 16:9764069-9764069 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3475C>T; p.R1159C; 16:9764069-9764069 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1491C>T; p.I497I; 16:9840942-9840942 |
skin; arm | malignant_melanoma | Substitution - coding silent |
c.2011C>T; p.Q671*; 16:9822421-9822421 |
adrenal_gland; adrenal_gland | adrenal_cortical_carcinoma; functioning | Substitution - Nonsense |
c.179C>T; p.A60V; 16:10180233-10180233 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.2426G>A; p.S809N; 16:9769020-9769020 |
skin | malignant_melanoma | Substitution - Missense |
c.363C>T; p.F121F; 16:10180049-10180049 |
skin | malignant_melanoma | Substitution - coding silent |
c.4229C>T; p.S1410L; 16:9763315-9763315 |
skin | malignant_melanoma | Substitution - Missense |
c.1532C>T; p.S511L; 16:9840766-9840766 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2671C>T; p.Q891*; 16:9764873-9764873 |
NS | malignant_melanoma | Substitution - Nonsense |
c.179C>T; p.A60V; 16:10180233-10180233 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1532C>T; p.S511L; 16:9840766-9840766 |
skin; neck | malignant_melanoma | Substitution - Missense |
c.363C>T; p.F121F; 16:10180049-10180049 |
skin | malignant_melanoma | Substitution - coding silent |
c.2451G>T; p.M817I; 16:9768995-9768995 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1532C>T; p.S511L; 16:9840766-9840766 |
skin | malignant_melanoma | Substitution - Missense |
c.3426C>T; p.P1142P; 16:9764118-9764118 |
skin | malignant_melanoma | Substitution - coding silent |
c.3426C>T; p.P1142P; 16:9764118-9764118 |
skin | malignant_melanoma | Substitution - coding silent |
c.2691C>T; p.L897L; 16:9764853-9764853 |
skin | malignant_melanoma | Substitution - coding silent |
c.181G>A; p.A61T; 16:10180231-10180231 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3855G>A; p.R1285R; 16:9763689-9763689 |
skin | malignant_melanoma | Substitution - coding silent |
c.3855G>A; p.R1285R; 16:9763689-9763689 |
skin | malignant_melanoma | Substitution - coding silent |
c.3395C>T; p.P1132L; 16:9764149-9764149 |
skin; ear | malignant_melanoma | Substitution - Missense |
c.2601C>A; p.I867I; 16:9764943-9764943 |
skin | malignant_melanoma | Substitution - coding silent |
c.3395C>T; p.P1132L; 16:9764149-9764149 |
skin | malignant_melanoma | Substitution - Missense |
c.2977C>A; p.P993T; 16:9764567-9764567 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.406G>C; p.A136P; 16:10180006-10180006 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2908C>T; p.R970W; 16:9764636-9764636 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2500A>C; p.T834P; 16:9768946-9768946 |
breast | carcinoma | Substitution - Missense |
c.754G>A; p.D252N; 16:9938212-9938212 |
skin | malignant_melanoma | Substitution - Missense |
c.155G>A; p.R52Q; 16:10180257-10180257 |
skin | malignant_melanoma | Substitution - Missense |
c.754G>A; p.D252N; 16:9938212-9938212 |
skin; arm | malignant_melanoma | Substitution - Missense |
c.3876C>T; p.Y1292Y; 16:9763668-9763668 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2856A>G; p.K952K; 16:9764688-9764688 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.794C>T; p.T265M; 16:9938172-9938172 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.450C>A; p.S150S; 16:9938516-9938516 |
skin; arm | malignant_melanoma | Substitution - coding silent |
c.4126C>T; p.R1376C; 16:9763418-9763418 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.3617G>T; p.R1206L; 16:9763927-9763927 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1121delA; p.K374fs*10; 16:9890987-9890987 |
pancreas | carcinoma; acinar_carcinoma | Deletion - Frameshift |
c.4126C>T; p.R1376C; 16:9763418-9763418 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3832C>A; p.Q1278K; 16:9763712-9763712 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.99G>A; p.A33A; 16:10180313-10180313 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.99G>A; p.A33A; 16:10180313-10180313 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.99G>A; p.A33A; 16:10180313-10180313 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2946A>G; p.G982G; 16:9764598-9764598 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.880G>A; p.D294N; 16:9938086-9938086 |
skin | malignant_melanoma | Substitution - Missense |
c.2721G>A; p.M907I; 16:9764823-9764823 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1391T>C; p.L464P; 16:9841042-9841042 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1757G>A; p.R586K; 16:9834125-9834125 |
skin | malignant_melanoma | Substitution - Missense |
c.325G>A; p.V109I; 16:10180087-10180087 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.3882C>A; p.N1294K; 16:9763662-9763662 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.817C>T; p.P273S; 16:9938149-9938149 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.1572C>G; p.F524L; 16:9840726-9840726 |
breast | carcinoma | Substitution - Missense |
c.700G>A; p.D234N; 16:9938266-9938266 |
skin | malignant_melanoma | Substitution - Missense |
c.132C>T; p.H44H; 16:10180280-10180280 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1516G>T; p.V506F; 16:9840782-9840782 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2145C>T; p.D715D; 16:9822287-9822287 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.748G>A; p.G250R; 16:9938218-9938218 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1303C>T; p.P435S; 16:9849781-9849781 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.372C>T; p.I124I; 16:10180040-10180040 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.4012G>A; p.G1338R; 16:9763532-9763532 |
skin | malignant_melanoma | Substitution - Missense |
c.388G>T; p.G130C; 16:10180024-10180024 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.415-1G>A; p.?; 16:9938552-9938552 |
skin | malignant_melanoma | Unknown |
c.1848C>T; p.S616S; 16:9829582-9829582 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - coding silent |
c.4071C>T; p.L1357L; 16:9763473-9763473 |
skin | malignant_melanoma | Substitution - coding silent |
c.2558G>C; p.C853S; 16:9768888-9768888 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1472A>T; p.N491I; 16:9840961-9840961 |
liver | carcinoma | Substitution - Missense |
c.363C>A; p.F121L; 16:10180049-10180049 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1813A>G; p.I605V; 16:9829617-9829617 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.222G>A; p.M74I; 16:10180190-10180190 |
skin | malignant_melanoma | Substitution - Missense |
c.3918G>A; p.R1306R; 16:9763626-9763626 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2071G>A; p.E691K; 16:9822361-9822361 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3443C>T; p.P1148L; 16:9764101-9764101 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3819G>A; p.Q1273Q; 16:9763725-9763725 |
skin | malignant_melanoma | Substitution - coding silent |
c.2659C>T; p.L887L; 16:9764885-9764885 |
skin | malignant_melanoma | Substitution - coding silent |
c.4324C>T; p.P1442S; 16:9763220-9763220 |
skin | malignant_melanoma | Substitution - Missense |
c.3246C>T; p.T1082T; 16:9764298-9764298 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.2659C>T; p.L887L; 16:9764885-9764885 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2265C>T; p.I755I; 16:9798368-9798368 |
skin | malignant_melanoma | Substitution - coding silent |
c.252G>A; p.T84T; 16:10180160-10180160 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4355G>A; p.R1452H; 16:9763189-9763189 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.4355G>A; p.R1452H; 16:9763189-9763189 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1594G>A; p.G532R; 16:9840704-9840704 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2120A>C; p.K707T; 16:9822312-9822312 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.4069C>T; p.L1357F; 16:9763475-9763475 |
skin | malignant_melanoma | Substitution - Missense |
c.3191C>T; p.T1064M; 16:9764353-9764353 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.4232A>G; p.Y1411C; 16:9763312-9763312 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.3191C>T; p.T1064M; 16:9764353-9764353 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.742C>T; p.L248F; 16:9938224-9938224 |
skin | malignant_melanoma | Substitution - Missense |
c.3346A>T; p.K1116*; 16:9764198-9764198 |
NS | malignant_melanoma | Substitution - Nonsense |
c.59G>A; p.G20D; 16:10180353-10180353 |
skin | malignant_melanoma | Substitution - Missense |
c.148G>A; p.E50K; 16:10180264-10180264 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.59G>A; p.G20D; 16:10180353-10180353 |
skin | malignant_melanoma | Substitution - Missense |
c.148G>A; p.E50K; 16:10180264-10180264 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4184C>T; p.A1395V; 16:9763360-9763360 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3315C>A; p.Y1105*; 16:9764229-9764229 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2657A>G; p.N886S; 16:9764887-9764887 |
pancreas | carcinoma | Substitution - Missense |
c.2657A>G; p.N886S; 16:9764887-9764887 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1927G>T; p.A643S; 16:9829503-9829503 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.313G>A; p.D105N; 16:10180099-10180099 |
skin | malignant_melanoma | Substitution - Missense |
c.2657A>G; p.N886S; 16:9764887-9764887 |
pancreas | carcinoma; ductal_carcinoma | Substitution - Missense |
c.2063G>A; p.G688E; 16:9822369-9822369 |
skin | malignant_melanoma | Substitution - Missense |
c.3333C>T; p.S1111S; 16:9764211-9764211 |
skin | malignant_melanoma | Substitution - coding silent |
c.2528G>A; p.W843*; 16:9768918-9768918 |
skin | malignant_melanoma | Substitution - Nonsense |
c.2063G>A; p.G688E; 16:9822369-9822369 |
skin | malignant_melanoma | Substitution - Missense |
c.1062C>A; p.G354G; 16:9891046-9891046 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3967A>T; p.N1323Y; 16:9763577-9763577 |
skin | malignant_melanoma | Substitution - Missense |
c.2614C>A; p.H872N; 16:9764930-9764930 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.3199C>T; p.R1067W; 16:9764345-9764345 |
skin | malignant_melanoma | Substitution - Missense |
c.3199C>T; p.R1067W; 16:9764345-9764345 |
breast | carcinoma | Substitution - Missense |
c.4021delA; p.S1341fs*56; 16:9763523-9763523 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.4021delA; p.S1341fs*56; 16:9763523-9763523 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.4021delA; p.S1341fs*56; 16:9763523-9763523 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.3199C>T; p.R1067W; 16:9764345-9764345 |
skin | malignant_melanoma | Substitution - Missense |
c.244C>T; p.L82F; 16:10180168-10180168 |
skin; trunk | malignant_melanoma; nodular | Substitution - Missense |
c.1299C>A; p.T433T; 16:9849785-9849785 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3555A>G; p.K1185K; 16:9763989-9763989 |
skin | malignant_melanoma | Substitution - coding silent |
c.4021delA; p.S1341fs*56; 16:9763523-9763523 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.3199C>T; p.R1067W; 16:9764345-9764345 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3199C>T; p.R1067W; 16:9764345-9764345 |
skin | malignant_melanoma | Substitution - Missense |
c.4021delA; p.S1341fs*56; 16:9763523-9763523 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.387G>A; p.G129G; 16:10180025-10180025 |
skin | malignant_melanoma | Substitution - coding silent |
c.4021delA; p.S1341fs*56; 16:9763523-9763523 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2814G>A; p.K938K; 16:9764730-9764730 |
skin | malignant_melanoma | Substitution - coding silent |
c.419C>T; p.P140L; 16:9938547-9938547 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1255G>A; p.V419M; 16:9849829-9849829 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1255G>A; p.V419M; 16:9849829-9849829 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.260G>T; p.C87F; 16:10180152-10180152 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.3635C>A; p.T1212K; 16:9763909-9763909 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.450C>T; p.S150S; 16:9938516-9938516 |
skin | malignant_melanoma | Substitution - coding silent |
c.833C>T; p.S278F; 16:9938133-9938133 |
NS | malignant_melanoma | Substitution - Missense |
c.833C>T; p.S278F; 16:9938133-9938133 |
skin | malignant_melanoma | Substitution - Missense |
c.833C>T; p.S278F; 16:9938133-9938133 |
skin | malignant_melanoma | Substitution - Missense |
c.2663C>T; p.T888M; 16:9764881-9764881 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2985G>A; p.T995T; 16:9764559-9764559 |
skin | malignant_melanoma | Substitution - coding silent |
c.2278G>A; p.G760S; 16:9798355-9798355 |
oesophagus | carcinoma | Substitution - Missense |
c.3316C>T; p.L1106L; 16:9764228-9764228 |
skin | malignant_melanoma | Substitution - coding silent |
c.4209G>C; p.S1403S; 16:9763335-9763335 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.3953G>A; p.R1318Q; 16:9763591-9763591 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.4321A>G; p.T1441A; 16:9763223-9763223 |
liver | carcinoma | Substitution - Missense |
c.4321A>G; p.T1441A; 16:9763223-9763223 |
liver | carcinoma | Substitution - Missense |
c.676G>A; p.V226I; 16:9938290-9938290 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3618A>G; p.R1206R; 16:9763926-9763926 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3571T>C; p.F1191L; 16:9763973-9763973 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3571T>C; p.F1191L; 16:9763973-9763973 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3571T>C; p.F1191L; 16:9763973-9763973 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3571T>C; p.F1191L; 16:9763973-9763973 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2460A>T; p.V820V; 16:9768986-9768986 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.4014G>A; p.G1338G; 16:9763530-9763530 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1629C>T; p.T543T; 16:9840669-9840669 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.727G>T; p.A243S; 16:9938239-9938239 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1629C>T; p.T543T; 16:9840669-9840669 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4014G>A; p.G1338G; 16:9763530-9763530 |
skin | malignant_melanoma | Substitution - coding silent |
c.3373G>A; p.E1125K; 16:9764171-9764171 |
skin | malignant_melanoma | Substitution - Missense |
c.128G>A; p.S43N; 16:10180284-10180284 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1162G>A; p.A388T; 16:9849922-9849922 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.964G>T; p.G322W; 16:9938002-9938002 |
breast | carcinoma | Substitution - Missense |
c.3926G>A; p.R1309Q; 16:9763618-9763618 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.315C>G; p.D105E; 16:10180097-10180097 |
breast | carcinoma | Substitution - Missense |
c.3373G>A; p.E1125K; 16:9764171-9764171 |
skin | malignant_melanoma | Substitution - Missense |
c.2406C>T; p.N802N; 16:9769040-9769040 |
liver | carcinoma | Substitution - coding silent |
c.3020A>G; p.N1007S; 16:9764524-9764524 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3766G>A; p.E1256K; 16:9763778-9763778 |
skin; acral | malignant_melanoma | Substitution - Missense |
c.1969G>A; p.E657K; 16:9829461-9829461 |
skin | malignant_melanoma | Substitution - Missense |
c.1521G>A; p.M507I; 16:9840777-9840777 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2937A>G; p.V979V; 16:9764607-9764607 |
bone; femur | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.2152G>A; p.V718I; 16:9822280-9822280 |
stomach | adenocarcinoma | Substitution - Missense |
c.1381A>T; p.I461F; 16:9841052-9841052 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2984C>T; p.T995M; 16:9764560-9764560 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.993G>A; p.M331I; 16:9937973-9937973 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2984C>T; p.T995M; 16:9764560-9764560 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2730G>A; p.M910I; 16:9764814-9764814 |
skin | malignant_melanoma | Substitution - Missense |
c.2861G>A; p.S954N; 16:9764683-9764683 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.74C>T; p.A25V; 16:10180338-10180338 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1751A>G; p.Y584C; 16:9834131-9834131 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3064C>T; p.R1022C; 16:9764480-9764480 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.4171T>G; p.L1391V; 16:9763373-9763373 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4114A>C; p.R1372R; 16:9763430-9763430 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.232G>A; p.D78N; 16:10180180-10180180 |
skin | malignant_melanoma | Substitution - Missense |
c.232G>A; p.D78N; 16:10180180-10180180 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.232G>A; p.D78N; 16:10180180-10180180 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3625C>A; p.Q1209K; 16:9763919-9763919 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.736C>A; p.L246I; 16:9938230-9938230 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.198C>T; p.D66D; 16:10180214-10180214 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3576C>T; p.T1192T; 16:9763968-9763968 |
skin | malignant_melanoma | Substitution - coding silent |
c.4393T>A; p.*1465K; 16:9763151-9763151 |
skin | malignant_melanoma | Nonstop extension |
c.4371G>T; p.M1457I; 16:9763173-9763173 |
skin | malignant_melanoma | Substitution - Missense |
c.3921C>A; p.P1307P; 16:9763623-9763623 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3474C>A; p.F1158L; 16:9764070-9764070 |
pleura | pulmonary_blastoma | Substitution - Missense |
c.2432A>T; p.Q811L; 16:9769014-9769014 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3269T>C; p.V1090A; 16:9764275-9764275 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4212C>T; p.S1404S; 16:9763332-9763332 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.3452A>G; p.Y1151C; 16:9764092-9764092 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3708C>A; p.C1236*; 16:9763836-9763836 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.3018G>A; p.A1006A; 16:9764526-9764526 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.3018G>A; p.A1006A; 16:9764526-9764526 |
skin | malignant_melanoma | Substitution - coding silent |
c.3018G>A; p.A1006A; 16:9764526-9764526 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.3399C>A; p.P1133P; 16:9764145-9764145 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3922T>C; p.S1308P; 16:9763622-9763622 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.4067C>A; p.S1356Y; 16:9763477-9763477 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2169-1G>A; p.?; 16:9798465-9798465 |
skin | malignant_melanoma | Unknown |
c.3018G>A; p.A1006A; 16:9764526-9764526 |
skin | malignant_melanoma | Substitution - coding silent |
c.4017A>G; p.K1339K; 16:9763527-9763527 |
skin | malignant_melanoma | Substitution - coding silent |
c.3505C>T; p.R1169W; 16:9764039-9764039 |
pancreas | carcinoma | Substitution - Missense |
c.2536C>A; p.R846S; 16:9768910-9768910 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1742C>T; p.P581L; 16:9834140-9834140 |
skin | malignant_melanoma | Substitution - Missense |
c.666C>G; p.I222M; 16:9938300-9938300 |
breast | carcinoma | Substitution - Missense |
c.2324T>C; p.I775T; 16:9798309-9798309 |
breast | carcinoma | Substitution - Missense |
c.3355A>C; p.T1119P; 16:9764189-9764189 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1737C>T; p.F579F; 16:9834145-9834145 |
skin; head_neck | malignant_melanoma; superficial_spreading | Substitution - coding silent |
c.2146G>A; p.A716T; 16:9822286-9822286 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.2332G>A; p.A778T; 16:9798301-9798301 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1311G>A; p.R437R; 16:9849773-9849773 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2146G>A; p.A716T; 16:9822286-9822286 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1898T>C; p.V633A; 16:9829532-9829532 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.681C>A; p.I227I; 16:9938285-9938285 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.306C>T; p.D102D; 16:10180106-10180106 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3526G>T; p.E1176*; 16:9764018-9764018 |
breast | carcinoma | Substitution - Nonsense |
c.657G>A; p.L219L; 16:9938309-9938309 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2075G>C; p.R692T; 16:9822357-9822357 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.4276G>A; p.E1426K; 16:9763268-9763268 |
skin; upper_leg | malignant_melanoma | Substitution - Missense |
c.2085G>C; p.R695R; 16:9822347-9822347 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1278C>T; p.T426T; 16:9849806-9849806 |
skin | malignant_melanoma | Substitution - coding silent |
c.2085G>C; p.R695R; 16:9822347-9822347 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1278C>T; p.T426T; 16:9849806-9849806 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1945C>T; p.L649L; 16:9829485-9829485 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2221A>G; p.R741G; 16:9798412-9798412 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.4208C>T; p.S1403L; 16:9763336-9763336 |
skin | malignant_melanoma | Substitution - Missense |
c.3176C>G; p.S1059C; 16:9764368-9764368 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1805G>A; p.G602E; 16:9829625-9829625 |
skin | malignant_melanoma | Substitution - Missense |
c.251C>T; p.T84M; 16:10180161-10180161 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3347A>C; p.K1116T; 16:9764197-9764197 |
breast | carcinoma | Substitution - Missense |
c.4354C>T; p.R1452C; 16:9763190-9763190 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.3510C>T; p.N1170N; 16:9764034-9764034 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1823T>C; p.L608P; 16:9829607-9829607 |
skin | malignant_melanoma | Substitution - Missense |
c.1485A>T; p.G495G; 16:9840948-9840948 |
lung; left_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3103G>A; p.D1035N; 16:9764441-9764441 |
skin; ear | malignant_melanoma | Substitution - Missense |
c.2880G>A; p.M960I; 16:9764664-9764664 |
breast | carcinoma | Substitution - Missense |
c.324C>T; p.A108A; 16:10180088-10180088 |
skin | malignant_melanoma | Substitution - coding silent |
c.1787G>A; p.G596E; 16:9829643-9829643 |
skin | malignant_melanoma | Substitution - Missense |
c.3812G>A; p.W1271*; 16:9763732-9763732 |
skin; foot | malignant_melanoma | Substitution - Nonsense |
c.1095G>T; p.V365V; 16:9891013-9891013 |
thyroid | other; neoplasm | Substitution - coding silent |
c.4340C>T; p.S1447F; 16:9763204-9763204 |
skin | malignant_melanoma | Substitution - Missense |
c.965G>A; p.G322E; 16:9938001-9938001 |
meninges | meningioma; haemangiopericytic | Substitution - Missense |
c.2191G>A; p.D731N; 16:9798442-9798442 |
skin | malignant_melanoma | Substitution - Missense |
c.2714C>T; p.S905F; 16:9764830-9764830 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.843C>T; p.Y281Y; 16:9938123-9938123 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2203T>A; p.L735M; 16:9798430-9798430 |
skin | malignant_melanoma | Substitution - Missense |
c.2714C>T; p.S905F; 16:9764830-9764830 |
skin | malignant_melanoma | Substitution - Missense |
c.436C>T; p.Q146*; 16:9938530-9938530 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2452G>A; p.A818T; 16:9768994-9768994 |
oesophagus | carcinoma | Substitution - Missense |
c.1308T>A; p.C436*; 16:9849776-9849776 |
liver | carcinoma | Substitution - Nonsense |
c.889G>A; p.G297S; 16:9938077-9938077 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3441C>T; p.F1147F; 16:9764103-9764103 |
skin | malignant_melanoma | Substitution - coding silent |
c.3597G>A; p.P1199P; 16:9763947-9763947 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3597G>A; p.P1199P; 16:9763947-9763947 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3441C>T; p.F1147F; 16:9764103-9764103 |
skin | malignant_melanoma | Substitution - coding silent |
c.3367G>T; p.E1123*; 16:9764177-9764177 |
prostate | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.3597G>A; p.P1199P; 16:9763947-9763947 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3120G>T; p.E1040D; 16:9764424-9764424 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1472A>G; p.N491S; 16:9840961-9840961 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1923C>T; p.F641F; 16:9829507-9829507 |
skin | malignant_melanoma | Substitution - coding silent |
c.2355T>C; p.D785D; 16:9798278-9798278 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.3248A>C; p.K1083T; 16:9764296-9764296 |
skin | malignant_melanoma | Substitution - Missense |
c.1165G>A; p.V389M; 16:9849919-9849919 |
kidney | carcinoma; renal_cell_carcinoma | Substitution - Missense |
c.3220C>T; p.P1074S; 16:9764324-9764324 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1592C>T; p.T531M; 16:9840706-9840706 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2067C>T; p.S689S; 16:9822365-9822365 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3284C>A; p.P1095H; 16:9764260-9764260 |
breast | carcinoma | Substitution - Missense |
c.920T>A; p.L307Q; 16:9938046-9938046 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.4097C>T; p.P1366L; 16:9763447-9763447 |
skin; ear | malignant_melanoma | Substitution - Missense |
c.3593C>T; p.S1198F; 16:9763951-9763951 |
skin | malignant_melanoma | Substitution - Missense |
c.3444G>T; p.P1148P; 16:9764100-9764100 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.3227A>G; p.N1076S; 16:9764317-9764317 |
pancreas | carcinoma; acinar_carcinoma | Substitution - Missense |
c.1778-8T>C; p.?; 16:9829660-9829660 |
lung | carcinoma; squamous_cell_carcinoma | Unknown |
c.111G>A; p.A37A; 16:10180301-10180301 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1983A>C; p.Q661H; 16:9829447-9829447 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1849G>T; p.V617L; 16:9829581-9829581 |
thyroid | carcinoma | Substitution - Missense |
c.3145C>A; p.P1049T; 16:9764399-9764399 |
liver | carcinoma | Substitution - Missense |
c.1087G>T; p.V363L; 16:9891021-9891021 |
prostate | carcinoma | Substitution - Missense |
c.2415C>T; p.N805N; 16:9769031-9769031 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2415C>T; p.N805N; 16:9769031-9769031 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2549C>T; p.T850M; 16:9768897-9768897 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3534T>G; p.L1178L; 16:9764010-9764010 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3686C>T; p.T1229I; 16:9763858-9763858 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2883C>T; p.N961N; 16:9764661-9764661 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2616T>A; p.H872Q; 16:9764928-9764928 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1279G>A; p.E427K; 16:9849805-9849805 |
skin | malignant_melanoma | Substitution - Missense |
c.4048G>A; p.D1350N; 16:9763496-9763496 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.4048G>A; p.D1350N; 16:9763496-9763496 |
skin | malignant_melanoma | Substitution - Missense |
c.1655C>T; p.P552L; 16:9834227-9834227 |
skin | malignant_melanoma | Substitution - Missense |
c.1376T>C; p.F459S; 16:9841057-9841057 |
skin | malignant_melanoma | Substitution - Missense |
c.1864C>T; p.P622S; 16:9829566-9829566 |
skin | malignant_melanoma | Substitution - Missense |
c.3466G>A; p.E1156K; 16:9764078-9764078 |
skin | malignant_melanoma | Substitution - Missense |
c.3466G>A; p.E1156K; 16:9764078-9764078 |
skin | malignant_melanoma | Substitution - Missense |
c.154C>T; p.R52*; 16:10180258-10180258 |
skin; ear | malignant_melanoma | Substitution - Nonsense |
c.4334T>G; p.L1445*; 16:9763210-9763210 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.4169C>T; p.S1390L; 16:9763375-9763375 |
skin | malignant_melanoma | Substitution - Missense |
c.1794T>G; p.S598S; 16:9829636-9829636 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1225G>A; p.V409I; 16:9849859-9849859 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.4169C>T; p.S1390L; 16:9763375-9763375 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1359G>T; p.K453N; 16:9841074-9841074 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.340G>A; p.D114N; 16:10180072-10180072 |
skin | malignant_melanoma | Substitution - Missense |
c.1794T>G; p.S598S; 16:9829636-9829636 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.3808G>C; p.D1270H; 16:9763736-9763736 |
skin | malignant_melanoma | Substitution - Missense |
c.1793C>T; p.S598F; 16:9829637-9829637 |
skin | malignant_melanoma | Substitution - Missense |
c.1172C>G; p.P391R; 16:9849912-9849912 |
ovary | other; neoplasm | Substitution - Missense |
c.3041G>T; p.W1014L; 16:9764503-9764503 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.4317C>A; p.Y1439*; 16:9763227-9763227 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.4071C>A; p.L1357L; 16:9763473-9763473 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3728G>T; p.G1243V; 16:9763816-9763816 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2393G>T; p.G798V; 16:9769053-9769053 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.3338C>T; p.P1113L; 16:9764206-9764206 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.3862C>T; p.R1288C; 16:9763682-9763682 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - Missense |
c.3862C>T; p.R1288C; 16:9763682-9763682 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3862C>T; p.R1288C; 16:9763682-9763682 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3728G>T; p.G1243V; 16:9763816-9763816 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.926A>C; p.K309T; 16:9938040-9938040 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1593G>T; p.T531T; 16:9840705-9840705 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1040A>C; p.D347A; 16:9891068-9891068 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.926A>C; p.K309T; 16:9938040-9938040 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3708C>T; p.C1236C; 16:9763836-9763836 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1384G>A; p.D462N; 16:9841049-9841049 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.423G>A; p.T141T; 16:9938543-9938543 |
pancreas | carcinoma | Substitution - coding silent |
c.1384G>A; p.D462N; 16:9841049-9841049 |
skin | malignant_melanoma | Substitution - Missense |
c.3708C>T; p.C1236C; 16:9763836-9763836 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2115G>C; p.M705I; 16:9822317-9822317 |
urinary_tract; bladder | carcinoma | Substitution - Missense |