General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 1523 |
Name | CUX1 |
Synonymous | cut-like homeobox 1;CUX1;cut-like homeobox 1 |
Definition | CCAAT displacement protein|cut homolog|golgi integral membrane protein 6|homeobox protein cux-1|protein CASP|putative protein product of Nbla10317 |
Position | 7q22.1 |
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 0.22. |
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.1942C>T; p.R648*; 7:102198849-102198849 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Nonsense |
c.2305G>A; p.A769T; 7:102201602-102201602 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.42T>C; p.D14D; 7:101916126-101916126 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4032T>C; p.T1344T; 7:102248556-102248556 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.442G>A; p.E148K; 7:102104371-102104371 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1393C>G; p.L465V; 7:102196804-102196804 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1750G>A; p.G584R; 7:102197161-102197161 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2780_2781insC; p.L930fs*24; 7:102202077-102202078 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Insertion - Frameshift |
c.3634C>T; p.R1212W; 7:102239331-102239331 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myeloid_leukaemia | Substitution - Missense |
c.3634C>T; p.R1212W; 7:102239331-102239331 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.4016A>T; p.D1339V; 7:102248540-102248540 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.2541C>T; p.G847G; 7:102201838-102201838 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1065G>A; p.K355K; 7:102189860-102189860 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.293G>A; p.G98E; 7:102097388-102097388 |
skin | malignant_melanoma | Substitution - Missense |
c.2645G>T; p.W882L; 7:102201942-102201942 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.4026G>T; p.E1342D; 7:102248550-102248550 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3062A>G; p.Q1021R; 7:102204545-102204545 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2220C>T; p.I740I; 7:102201517-102201517 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2220C>T; p.I740I; 7:102201517-102201517 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.657T>C; p.D219D; 7:102115256-102115256 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2274A>G; p.P758P; 7:102201571-102201571 |
thyroid | other; neoplasm | Substitution - coding silent |
c.2274A>G; p.P758P; 7:102201571-102201571 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.183A>C; p.Q61H; 7:102028139-102028139 |
liver | carcinoma | Substitution - Missense |
c.1342A>G; p.T448A; 7:102196753-102196753 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2447G>A; p.R816H; 7:102201744-102201744 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1610G>T; p.S537I; 7:102197021-102197021 |
liver | carcinoma | Substitution - Missense |
c.1943G>A; p.R648Q; 7:102198850-102198850 |
breast | carcinoma | Substitution - Missense |
c.3433+1G>T; p.?; 7:102227670-102227670 |
lung | carcinoma; squamous_cell_carcinoma | Unknown |
c.1943G>A; p.R648Q; 7:102198850-102198850 |
skin | malignant_melanoma | Substitution - Missense |
c.1100C>T; p.A367V; 7:102193865-102193865 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3084C>T; p.S1028S; 7:102205124-102205124 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.691_692insAA; p.M231fs*2; 7:102158576-102158577 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; polycythaemia_vera | Insertion - Frameshift |
c.2777C>T; p.S926L; 7:102202074-102202074 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2336C>T; p.P779L; 7:102201633-102201633 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1213G>A; p.D405N; 7:102195594-102195594 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.3682G>C; p.V1228L; 7:102239379-102239379 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_leukaemic_transformation_of_essential_thrombocythaemia | Substitution - Missense |
c.201G>C; p.L67L; 7:102070350-102070350 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.201G>C; p.L67L; 7:102070350-102070350 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.3327C>A; p.S1109S; 7:102227563-102227563 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.508A>G; p.N170D; 7:102104437-102104437 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.3037G>A; p.G1013S; 7:102204520-102204520 |
skin | malignant_melanoma | Substitution - Missense |
c.1131G>A; p.A377A; 7:102195512-102195512 |
breast | carcinoma | Substitution - coding silent |
c.3229C>T; p.P1077S; 7:102227465-102227465 |
skin | malignant_melanoma | Substitution - Missense |
c.2941A>G; p.M981V; 7:102204424-102204424 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3758C>T; p.P1253L; 7:102239455-102239455 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.432G>A; p.E144E; 7:102104361-102104361 |
skin | malignant_melanoma | Substitution - coding silent |
c.3048C>T; p.P1016P; 7:102204531-102204531 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.993G>T; p.L331L; 7:102178633-102178633 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3742C>T; p.R1248W; 7:102239439-102239439 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1902_1902delA; p.G635fs*4; 7:102198809-102198809 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Deletion - Frameshift |
c.41A>T; p.D14V; 7:101916125-101916125 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.3742C>T; p.R1248W; 7:102239439-102239439 |
skin | malignant_melanoma | Substitution - Missense |
c.2224_2225insC; p.K744fs*29; 7:102201521-102201522 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Insertion - Frameshift |
c.2445C>T; p.G815G; 7:102201742-102201742 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.655G>A; p.D219N; 7:102115254-102115254 |
skin | malignant_melanoma | Substitution - Missense |
c.2860G>A; p.E954K; 7:102202157-102202157 |
breast | carcinoma | Substitution - Missense |
c.3204G>T; p.K1068N; 7:102227440-102227440 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.3743G>T; p.R1248L; 7:102239440-102239440 |
liver | carcinoma | Substitution - Missense |
c.2233C>A; p.L745I; 7:102201530-102201530 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2498_2500delGAA; p.R833delR; 7:102201795-102201797 |
prostate | carcinoma | Deletion - In frame |
c.3743G>T; p.R1248L; 7:102239440-102239440 |
liver | carcinoma | Substitution - Missense |
c.810C>G; p.I270M; 7:102170532-102170532 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3306C>A; p.P1102P; 7:102227542-102227542 |
skin | malignant_melanoma | Substitution - coding silent |
c.2119C>T; p.R707C; 7:102201416-102201416 |
skin | malignant_melanoma | Substitution - Missense |
c.661G>T; p.E221*; 7:102115260-102115260 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.4346delC; p.R1451fs*34; 7:102248870-102248870 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.1775G>A; p.R592Q; 7:102197186-102197186 |
thyroid | carcinoma; anaplastic_carcinoma | Substitution - Missense |
c.418A>G; p.K140E; 7:102104347-102104347 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.3510C>A; p.P1170P; 7:102234128-102234128 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2605C>T; p.Q869*; 7:102201902-102201902 |
large_intestine; colon | carcinoma | Substitution - Nonsense |
c.2605C>T; p.Q869*; 7:102201902-102201902 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.4429C>A; p.R1477S; 7:102248953-102248953 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2238G>A; p.L746L; 7:102201535-102201535 |
breast | carcinoma | Substitution - coding silent |
c.1125+2T>C; p.?; 7:102193892-102193892 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.2742C>T; p.S914S; 7:102202039-102202039 |
skin | malignant_melanoma | Substitution - coding silent |
c.1558C>T; p.Q520*; 7:102196969-102196969 |
skin | malignant_melanoma | Substitution - Nonsense |
c.2357_2358insA; p.E787fs*27; 7:102201654-102201655 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Insertion - Frameshift |
c.2446C>T; p.R816C; 7:102201743-102201743 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2076G>C; p.Q692H; 7:102201373-102201373 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2786_2787insC; p.L930fs*24; 7:102202083-102202084 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Insertion - Frameshift |
c.3934A>G; p.S1312G; 7:102248458-102248458 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.4512G>T; p.E1504D; 7:102249036-102249036 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3236C>T; p.P1079L; 7:102227472-102227472 |
skin | malignant_melanoma | Substitution - Missense |
c.1282G>C; p.A428P; 7:102196693-102196693 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2986C>T; p.R996*; 7:102204469-102204469 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Nonsense |
c.2986C>T; p.R996*; 7:102204469-102204469 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Substitution - Nonsense |
c.1282G>C; p.A428P; 7:102196693-102196693 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4139C>T; p.T1380I; 7:102248663-102248663 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2332C>T; p.L778L; 7:102201629-102201629 |
skin | malignant_melanoma | Substitution - coding silent |
c.2731_2732insC; p.L911fs*43; 7:102202028-102202029 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Insertion - Frameshift |
c.2229_2230insC; p.K744fs*29; 7:102201526-102201527 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Insertion - Frameshift |
c.1989_1990GG>TT; p.S663>?; 7:102200099-102200100 |
lung | carcinoma; adenocarcinoma | Complex |
c.1607C>A; p.P536H; 7:102197018-102197018 |
prostate | carcinoma | Substitution - Missense |
c.3105G>A; p.P1035P; 7:102205145-102205145 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2763G>A; p.K921K; 7:102202060-102202060 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2699C>T; p.A900V; 7:102201996-102201996 |
prostate | carcinoma | Substitution - Missense |
c.2096G>T; p.S699I; 7:102201393-102201393 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2530G>A; p.E844K; 7:102201827-102201827 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2307A>G; p.A769A; 7:102201604-102201604 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1046C>T; p.A349V; 7:102189841-102189841 |
breast | carcinoma | Substitution - Missense |
c.601C>T; p.Q201*; 7:102111768-102111768 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1457G>A; p.R486Q; 7:102196868-102196868 |
soft_tissue; striated_muscle | rhabdomyosarcoma; embryonal | Substitution - Missense |
c.451C>T; p.Q151*; 7:102104380-102104380 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; Burkitt_lymphoma | Substitution - Nonsense |
c.1076+5G>A; p.?; 7:102189876-102189876 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Unknown |
c.710_710delA; p.R238fs*16; 7:102158595-102158595 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Deletion - Frameshift |
c.3573C>A; p.D1191E; 7:102234191-102234191 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2538G>A; p.T846T; 7:102201835-102201835 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.879C>T; p.A293A; 7:102178519-102178519 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2340delC; p.P782fs*26; 7:102201637-102201637 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myelomonocytic_leukaemia | Deletion - Frameshift |
c.2318C>T; p.A773V; 7:102201615-102201615 |
skin | malignant_melanoma | Substitution - Missense |
c.2744C>T; p.P915L; 7:102202041-102202041 |
skin | malignant_melanoma | Substitution - Missense |
c.2345_2346insC; p.A783fs*31; 7:102201642-102201643 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Insertion - Frameshift |
c.2744C>T; p.P915L; 7:102202041-102202041 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.4503C>T; p.I1501I; 7:102249027-102249027 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2768C>G; p.T923S; 7:102202065-102202065 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2694C>T; p.T898T; 7:102201991-102201991 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2987G>A; p.R996Q; 7:102204470-102204470 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.3538G>T; p.E1180*; 7:102234156-102234156 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2727delC; p.L911fs*20; 7:102202024-102202024 |
large_intestine; rectum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.181C>T; p.Q61*; 7:102028137-102028137 |
skin | malignant_melanoma | Substitution - Nonsense |
c.370G>T; p.E124*; 7:102097465-102097465 |
breast | carcinoma | Substitution - Nonsense |
c.303C>T; p.L101L; 7:102097398-102097398 |
skin | malignant_melanoma | Substitution - coding silent |
c.622C>T; p.R208*; 7:102115221-102115221 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.622C>T; p.R208*; 7:102115221-102115221 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.2188C>T; p.Q730*; 7:102201485-102201485 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.97C>T; p.R33W; 7:101916181-101916181 |
liver | carcinoma | Substitution - Missense |
c.622C>T; p.R208*; 7:102115221-102115221 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.622C>T; p.R208*; 7:102115221-102115221 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.622C>T; p.R208*; 7:102115221-102115221 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.97C>T; p.R33W; 7:101916181-101916181 |
liver | carcinoma | Substitution - Missense |
c.622C>T; p.R208*; 7:102115221-102115221 |
skin; trunk | malignant_melanoma | Substitution - Nonsense |
c.2734C>T; p.P912S; 7:102202031-102202031 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.623G>A; p.R208Q; 7:102115222-102115222 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.689A>G; p.E230G; 7:102158574-102158574 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2847C>T; p.T949T; 7:102202144-102202144 |
skin | malignant_melanoma | Substitution - coding silent |
c.897C>T; p.I299I; 7:102178537-102178537 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3388G>T; p.G1130C; 7:102227624-102227624 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.897C>T; p.I299I; 7:102178537-102178537 |
skin | malignant_melanoma | Substitution - coding silent |
c.2215A>G; p.T739A; 7:102201512-102201512 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.682G>A; p.E228K; 7:102158567-102158567 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2446C>A; p.R816S; 7:102201743-102201743 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.131A>G; p.N44S; 7:101916215-101916215 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2371G>A; p.A791T; 7:102201668-102201668 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4464C>T; p.I1488I; 7:102248988-102248988 |
skin | malignant_melanoma | Substitution - coding silent |
c.739C>T; p.Q247*; 7:102170461-102170461 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.1818A>T; p.P606P; 7:102197229-102197229 |
breast | carcinoma | Substitution - coding silent |
c.2833A>T; p.T945S; 7:102202130-102202130 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.169C>T; p.L57L; 7:102028125-102028125 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1375G>T; p.D459Y; 7:102196786-102196786 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.301C>T; p.L101F; 7:102097396-102097396 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Substitution - Missense |
c.3082T>A; p.S1028T; 7:102205122-102205122 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3583G>T; p.V1195L; 7:102234201-102234201 |
thyroid | carcinoma | Substitution - Missense |
c.3815A>T; p.K1272I; 7:102239512-102239512 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1960+1G>T; p.?; 7:102198868-102198868 |
lung | carcinoma; adenocarcinoma | Unknown |
c.1494G>T; p.Q498H; 7:102196905-102196905 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1269G>A; p.P423P; 7:102196680-102196680 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1269G>A; p.P423P; 7:102196680-102196680 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.3513G>A; p.W1171*; 7:102234131-102234131 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myelomonocytic_leukaemia | Substitution - Nonsense |
c.2384A>G; p.D795G; 7:102201681-102201681 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2257A>G; p.T753A; 7:102201554-102201554 |
pancreas | carcinoma | Substitution - Missense |
c.847C>T; p.L283L; 7:102178487-102178487 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.106G>A; p.E36K; 7:101916190-101916190 |
endometrium | carcinoma; serous_carcinoma | Substitution - Missense |
c.106G>A; p.E36K; 7:101916190-101916190 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.106G>A; p.E36K; 7:101916190-101916190 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.217G>A; p.E73K; 7:102070366-102070366 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.106G>A; p.E36K; 7:101916190-101916190 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.106G>A; p.E36K; 7:101916190-101916190 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3271G>C; p.E1091Q; 7:102227507-102227507 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.990G>T; p.Q330H; 7:102178630-102178630 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.825C>T; p.D275D; 7:102170547-102170547 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2966delG; p.S989fs*3; 7:102204449-102204449 |
lung | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1812G>T; p.K604N; 7:102197223-102197223 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1528G>T; p.G510C; 7:102196939-102196939 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2556_2557insGGCAGCGGT; p.K852_G853insGSG; 7:102201853-102201854 |
breast | carcinoma | Insertion - In frame |
c.507G>A; p.Q169Q; 7:102104436-102104436 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2556_2557insGGCAGCGGT; p.K852_G853insGSG; 7:102201853-102201854 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Insertion - In frame |
c.1645G>T; p.E549*; 7:102197056-102197056 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.1024G>T; p.E342*; 7:102189819-102189819 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.3499C>T; p.R1167C; 7:102234117-102234117 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.841G>C; p.E281Q; 7:102178481-102178481 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3499C>T; p.R1167C; 7:102234117-102234117 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.3433G>A; p.G1145S; 7:102227669-102227669 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.136C>T; p.P46S; 7:101916220-101916220 |
skin | malignant_melanoma | Substitution - Missense |
c.2662C>G; p.P888A; 7:102201959-102201959 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.3245A>G; p.E1082G; 7:102227481-102227481 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2319C>T; p.A773A; 7:102201616-102201616 |
skin | malignant_melanoma | Substitution - coding silent |
c.1644C>T; p.G548G; 7:102197055-102197055 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1751G>A; p.G584E; 7:102197162-102197162 |
skin | malignant_melanoma | Substitution - Missense |
c.3855C>A; p.T1285T; 7:102239552-102239552 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3235delC; p.I1081fs*39; 7:102227471-102227471 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.3235delC; p.I1081fs*39; 7:102227471-102227471 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1672C>T; p.R558W; 7:102197083-102197083 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1822C>T; p.H608Y; 7:102197233-102197233 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1316G>T; p.G439V; 7:102196727-102196727 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.2974A>T; p.T992S; 7:102204457-102204457 |
skin | malignant_melanoma | Substitution - Missense |
c.666T>C; p.T222T; 7:102115265-102115265 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.539A>C; p.Q180P; 7:102111706-102111706 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.2905A>G; p.K969E; 7:102202202-102202202 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3432C>T; p.L1144L; 7:102227668-102227668 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3432C>T; p.L1144L; 7:102227668-102227668 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1708G>A; p.G570R; 7:102197119-102197119 |
skin | malignant_melanoma | Substitution - Missense |
c.1400G>T; p.S467I; 7:102196811-102196811 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Substitution - Missense |
c.1580C>T; p.P527L; 7:102196991-102196991 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.915C>T; p.D305D; 7:102178555-102178555 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.915C>T; p.D305D; 7:102178555-102178555 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2931C>T; p.S977S; 7:102204414-102204414 |
liver | carcinoma | Substitution - coding silent |
c.4380C>T; p.F1460F; 7:102248904-102248904 |
skin | malignant_melanoma | Substitution - coding silent |
c.1283delC; p.P430fs*27; 7:102196694-102196694 |
large_intestine; rectum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.876G>T; p.L292F; 7:102178516-102178516 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1283delC; p.P430fs*27; 7:102196694-102196694 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.876G>T; p.L292F; 7:102178516-102178516 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1283delC; p.P430fs*27; 7:102196694-102196694 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.1738G>T; p.G580*; 7:102197149-102197149 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.3781C>T; p.R1261*; 7:102239478-102239478 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Substitution - Nonsense |
c.4317G>A; p.P1439P; 7:102248841-102248841 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1114G>A; p.A372T; 7:102193879-102193879 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.4317G>A; p.P1439P; 7:102248841-102248841 |
thyroid | other; neoplasm | Substitution - coding silent |
c.4317G>A; p.P1439P; 7:102248841-102248841 |
thyroid | other; neoplasm | Substitution - coding silent |
c.4317G>A; p.P1439P; 7:102248841-102248841 |
thyroid | other; neoplasm | Substitution - coding silent |
c.3861C>T; p.T1287T; 7:102239558-102239558 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1264C>T; p.R422C; 7:102196675-102196675 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1747C>T; p.Q583*; 7:102197158-102197158 |
skin | malignant_melanoma | Substitution - Nonsense |
c.3680C>T; p.S1227F; 7:102239377-102239377 |
skin | malignant_melanoma | Substitution - Missense |
c.2978A>T; p.Q993L; 7:102204461-102204461 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2510C>T; p.S837F; 7:102201807-102201807 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2712G>T; p.E904D; 7:102202009-102202009 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.749C>T; p.A250V; 7:102170471-102170471 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3951C>A; p.G1317G; 7:102248475-102248475 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.2674A>C; p.S892R; 7:102201971-102201971 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3025G>A; p.E1009K; 7:102204508-102204508 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Substitution - Missense |
c.3193G>T; p.E1065*; 7:102227429-102227429 |
thyroid | carcinoma | Substitution - Nonsense |
c.1189G>A; p.A397T; 7:102195570-102195570 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.678C>T; p.A226A; 7:102158563-102158563 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2370C>T; p.D790D; 7:102201667-102201667 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1804C>A; p.R602S; 7:102197215-102197215 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1286C>T; p.P429L; 7:102196697-102196697 |
skin | malignant_melanoma | Substitution - Missense |
c.1104G>A; p.P368P; 7:102193869-102193869 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2107G>A; p.D703N; 7:102201404-102201404 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2955G>A; p.P985P; 7:102204438-102204438 |
thyroid | carcinoma | Substitution - coding silent |
c.3535C>T; p.R1179*; 7:102234153-102234153 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myelomonocytic_leukaemia | Substitution - Nonsense |
c.1104G>A; p.P368P; 7:102193869-102193869 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3535C>T; p.R1179*; 7:102234153-102234153 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Substitution - Nonsense |
c.3786G>T; p.A1262A; 7:102239483-102239483 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1281G>A; p.P427P; 7:102196692-102196692 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1543A>G; p.N515D; 7:102196954-102196954 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.105C>T; p.I35I; 7:101916189-101916189 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1938G>A; p.P646P; 7:102198845-102198845 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2220C>A; p.I740I; 7:102201517-102201517 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1938G>A; p.P646P; 7:102198845-102198845 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1313C>T; p.P438L; 7:102196724-102196724 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2753C>T; p.P918L; 7:102202050-102202050 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2622G>A; p.S874S; 7:102201919-102201919 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.247A>T; p.K83*; 7:102070396-102070396 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.3887G>A; p.R1296K; 7:102239584-102239584 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Substitution - Missense |
c.2529C>T; p.A843A; 7:102201826-102201826 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2745G>A; p.P915P; 7:102202042-102202042 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3485C>T; p.S1162F; 7:102234103-102234103 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2320G>A; p.G774S; 7:102201617-102201617 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3781C>A; p.R1261R; 7:102239478-102239478 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.2869_2870insG; p.A957fs*102; 7:102202166-102202167 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myelomonocytic_leukaemia | Insertion - Frameshift |
c.1946G>T; p.R649I; 7:102198853-102198853 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3163C>A; p.P1055T; 7:102227399-102227399 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.4470C>T; p.R1490R; 7:102248994-102248994 |
skin | malignant_melanoma | Substitution - coding silent |
c.142-1G>A; p.?; 7:102028097-102028097 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myelomonocytic_leukaemia | Unknown |
c.142-1G>A; p.?; 7:102028097-102028097 |
skin | malignant_melanoma | Unknown |
c.4401C>T; p.G1467G; 7:102248925-102248925 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3261C>T; p.S1087S; 7:102227497-102227497 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.49G>A; p.A17T; 7:101916133-101916133 |
prostate | carcinoma | Substitution - Missense |
c.4401C>T; p.G1467G; 7:102248925-102248925 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.789C>T; p.S263S; 7:102170511-102170511 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2646G>T; p.W882C; 7:102201943-102201943 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1577G>C; p.S526T; 7:102196988-102196988 |
pancreas | carcinoma | Substitution - Missense |
c.1577G>C; p.S526T; 7:102196988-102196988 |
pancreas | carcinoma | Substitution - Missense |
c.608-2A>C; p.?; 7:102115205-102115205 |
large_intestine; caecum | carcinoma; adenocarcinoma | Unknown |
c.3401G>A; p.R1134Q; 7:102227637-102227637 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1199G>A; p.R400H; 7:102195580-102195580 |
prostate | carcinoma | Substitution - Missense |
c.3910T>G; p.F1304V; 7:102248434-102248434 |
liver | carcinoma | Substitution - Missense |
c.3910T>G; p.F1304V; 7:102248434-102248434 |
liver | carcinoma | Substitution - Missense |
c.3793C>T; p.Q1265*; 7:102239490-102239490 |
ovary | carcinoma; serous_carcinoma | Substitution - Nonsense |
c.1282_1283insC; p.P431fs*16; 7:102196693-102196694 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.161C>T; p.A54V; 7:102028117-102028117 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3898C>T; p.R1300C; 7:102248422-102248422 |
skin | malignant_melanoma | Substitution - Missense |
c.1668C>T; p.I556I; 7:102197079-102197079 |
skin | malignant_melanoma | Substitution - coding silent |
c.2305delG; p.A769fs*39; 7:102201602-102201602 |
breast | carcinoma | Deletion - Frameshift |
c.1105T>C; p.S369P; 7:102193870-102193870 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3000C>T; p.I1000I; 7:102204483-102204483 |
skin | malignant_melanoma | Substitution - coding silent |
c.1193C>T; p.A398V; 7:102195574-102195574 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.61G>A; p.A21T; 7:101916145-101916145 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1193C>T; p.A398V; 7:102195574-102195574 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.261C>T; p.D87D; 7:102070410-102070410 |
breast | carcinoma | Substitution - coding silent |
c.1804C>T; p.R602C; 7:102197215-102197215 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1804C>T; p.R602C; 7:102197215-102197215 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2009C>T; p.A670V; 7:102200119-102200119 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Substitution - Missense |
c.1269G>C; p.P423P; 7:102196680-102196680 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3465G>A; p.G1155G; 7:102234083-102234083 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; Burkitt_lymphoma | Substitution - coding silent |
c.1806T>G; p.R602R; 7:102197217-102197217 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1921C>G; p.L641V; 7:102198828-102198828 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1638C>T; p.S546S; 7:102197049-102197049 |
skin | malignant_melanoma | Substitution - coding silent |
c.2376C>T; p.P792P; 7:102201673-102201673 |
skin | malignant_melanoma | Substitution - coding silent |
c.966C>G; p.S322R; 7:102178606-102178606 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.769C>A; p.L257I; 7:102170491-102170491 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.701C>T; p.T234M; 7:102158586-102158586 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.327C>T; p.H109H; 7:102097422-102097422 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1166A>G; p.N389S; 7:102195547-102195547 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.3813delA; p.T1273fs*11; 7:102239510-102239510 |
skin | malignant_melanoma | Deletion - Frameshift |
c.3813delA; p.T1273fs*11; 7:102239510-102239510 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2849G>C; p.R950P; 7:102202146-102202146 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1281G>C; p.P427P; 7:102196692-102196692 |
skin | malignant_melanoma | Substitution - coding silent |
c.1427G>A; p.G476E; 7:102196838-102196838 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2898C>T; p.F966F; 7:102202195-102202195 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1038A>T; p.K346N; 7:102189833-102189833 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.608-1G>T; p.?; 7:102115206-102115206 |
endometrium | carcinoma; serous_carcinoma | Unknown |
c.391G>A; p.E131K; 7:102097486-102097486 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2118C>T; p.I706I; 7:102201415-102201415 |
skin | malignant_melanoma | Substitution - coding silent |
c.391G>A; p.E131K; 7:102097486-102097486 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2202C>T; p.S734S; 7:102201499-102201499 |
skin; arm | malignant_melanoma | Substitution - coding silent |
c.2335C>T; p.P779S; 7:102201632-102201632 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2132A>G; p.Q711R; 7:102201429-102201429 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.339_340delAG; p.N115fs*4; 7:102097434-102097435 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Deletion - Frameshift |
c.421delG; p.A141fs*13; 7:102104350-102104350 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myelomonocytic_leukaemia | Deletion - Frameshift |
c.3175_3176insC; p.M1061fs*5; 7:102227411-102227412 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myelomonocytic_leukaemia | Insertion - Frameshift |
c.1024G>A; p.E342K; 7:102189819-102189819 |
salivary_gland; parotid | carcinoma; adenoid_cystic_carcinoma | Substitution - Missense |
c.2463G>A; p.K821K; 7:102201760-102201760 |
skin | malignant_melanoma | Substitution - coding silent |
c.2387C>A; p.P796H; 7:102201684-102201684 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.3017T>C; p.L1006P; 7:102204500-102204500 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3505A>C; p.K1169Q; 7:102234123-102234123 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myelomonocytic_leukaemia | Substitution - Missense |
c.2388C>T; p.P796P; 7:102201685-102201685 |
skin | malignant_melanoma | Substitution - coding silent |
c.410delT; p.T138fs*2; 7:102104339-102104339 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelodysplastic_syndrome | Deletion - Frameshift |
c.44C>T; p.A15V; 7:101916128-101916128 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.439C>T; p.R147*; 7:102104368-102104368 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.439C>T; p.R147*; 7:102104368-102104368 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.2861A>G; p.E954G; 7:102202158-102202158 |
skin | malignant_melanoma | Substitution - Missense |
c.1982G>T; p.R661L; 7:102200092-102200092 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.3489C>T; p.D1163D; 7:102234107-102234107 |
skin | malignant_melanoma | Substitution - coding silent |
c.137C>A; p.P46Q; 7:101916221-101916221 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.262G>A; p.V88I; 7:102070411-102070411 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2774C>T; p.P925L; 7:102202071-102202071 |
skin | malignant_melanoma | Substitution - Missense |
c.3929C>T; p.A1310V; 7:102248453-102248453 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.406G>A; p.E136K; 7:102097501-102097501 |
pancreas | NS | Substitution - Missense |
c.251_254delGATT; p.I86fs*46; 7:102070400-102070403 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Deletion - Frameshift |
c.1090A>G; p.M364V; 7:102193855-102193855 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3190A>C; p.S1064R; 7:102227426-102227426 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3786G>A; p.A1262A; 7:102239483-102239483 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.3786G>A; p.A1262A; 7:102239483-102239483 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2634C>A; p.Y878*; 7:102201931-102201931 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.945G>A; p.K315K; 7:102178585-102178585 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2542G>A; p.G848S; 7:102201839-102201839 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |