| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 3371 | ||
Name | TNC | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1371G>A; p.E457E; 9:115086360-115086360 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.693C>T; p.C231C; 9:115087038-115087038 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.693C>T; p.C231C; 9:115087038-115087038 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1062C>T; p.G354G; 9:115086669-115086669 |
skin | malignant_melanoma | Substitution - coding silent |
c.4442C>A; p.T1481N; 9:115057290-115057290 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1312C>T; p.R438W; 9:115086419-115086419 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.5666C>T; p.S1889F; 9:115035325-115035325 |
skin | malignant_melanoma | Substitution - Missense |
c.1313G>A; p.R438Q; 9:115086418-115086418 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.3379C>T; p.R1127W; 9:115064755-115064755 |
skin | malignant_melanoma | Substitution - Missense |
c.4775G>A; p.G1592D; 9:115048337-115048337 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.4838C>T; p.A1613V; 9:115048274-115048274 |
skin | malignant_melanoma | Substitution - Missense |
c.1633G>A; p.G545R; 9:115086098-115086098 |
skin | malignant_melanoma | Substitution - Missense |
c.366G>T; p.L122L; 9:115090653-115090653 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.6145G>A; p.D2049N; 9:115029384-115029384 |
skin | malignant_melanoma | Substitution - Missense |
c.196G>T; p.V66L; 9:115090823-115090823 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.4746G>A; p.R1582R; 9:115048366-115048366 |
skin | malignant_melanoma | Substitution - coding silent |
c.5605G>A; p.A1869T; 9:115036149-115036149 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.5087G>A; p.G1696E; 9:115046448-115046448 |
skin | malignant_melanoma | Substitution - Missense |
c.209C>T; p.S70L; 9:115090810-115090810 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.6348C>A; p.Y2116*; 9:115024120-115024120 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.1035C>A; p.T345T; 9:115086696-115086696 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3490G>A; p.E1164K; 9:115064066-115064066 |
skin | malignant_melanoma | Substitution - Missense |
c.4233G>A; p.T1411T; 9:115059803-115059803 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1971G>A; p.T657T; 9:115084369-115084369 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5691G>C; p.E1897D; 9:115035300-115035300 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.5452A>G; p.R1818G; 9:115038321-115038321 |
skin | malignant_melanoma | Substitution - Missense |
c.3938T>C; p.I1313T; 9:115063012-115063012 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3040C>T; p.R1014C; 9:115073777-115073777 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.299T>C; p.F100S; 9:115090720-115090720 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2034C>A; p.I678I; 9:115084306-115084306 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.2852C>T; p.T951I; 9:115076398-115076398 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.6169+1G>T; p.?; 9:115029359-115029359 |
prostate | carcinoma; adenocarcinoma | Unknown |
c.5057A>T; p.Y1686F; 9:115046478-115046478 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.717C>T; p.F239F; 9:115087014-115087014 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.717C>T; p.F239F; 9:115087014-115087014 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.717C>T; p.F239F; 9:115087014-115087014 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.342C>T; p.A114A; 9:115090677-115090677 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.4624C>T; p.P1542S; 9:115048488-115048488 |
skin | malignant_melanoma | Substitution - Missense |
c.2071C>T; p.R691C; 9:115084269-115084269 |
skin | malignant_melanoma | Substitution - Missense |
c.4997T>G; p.I1666R; 9:115046538-115046538 |
skin | malignant_melanoma | Substitution - Missense |
c.810C>T; p.C270C; 9:115086921-115086921 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1575T>G; p.P525P; 9:115086156-115086156 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4983T>G; p.S1661S; 9:115046552-115046552 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.6273C>T; p.S2091S; 9:115026592-115026592 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2576C>A; p.S859Y; 9:115078041-115078041 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.2336A>T; p.Y779F; 9:115081840-115081840 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.5316C>T; p.G1772G; 9:115041017-115041017 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3082G>A; p.G1028R; 9:115073735-115073735 |
skin | malignant_melanoma | Substitution - Missense |
c.3981C>T; p.H1327H; 9:115062969-115062969 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3981C>T; p.H1327H; 9:115062969-115062969 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3981C>T; p.H1327H; 9:115062969-115062969 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4206G>T; p.V1402V; 9:115059830-115059830 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.696A>G; p.V232V; 9:115087035-115087035 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5689G>A; p.E1897K; 9:115035302-115035302 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.5689G>A; p.E1897K; 9:115035302-115035302 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1809A>G; p.Q603Q; 9:115085922-115085922 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1706G>A; p.G569D; 9:115086025-115086025 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1356C>T; p.G452G; 9:115086375-115086375 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1905G>A; p.T635T; 9:115084435-115084435 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4746G>C; p.R1582S; 9:115048366-115048366 |
skin; scalp | malignant_melanoma | Substitution - Missense |
c.4140G>T; p.Q1380H; 9:115059896-115059896 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.718G>A; p.E240K; 9:115087013-115087013 |
skin | malignant_melanoma | Substitution - Missense |
c.4140G>T; p.Q1380H; 9:115059896-115059896 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.718G>A; p.E240K; 9:115087013-115087013 |
skin | malignant_melanoma | Substitution - Missense |
c.4140G>T; p.Q1380H; 9:115059896-115059896 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2039A>G; p.Q680R; 9:115084301-115084301 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2039A>G; p.Q680R; 9:115084301-115084301 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.4714C>A; p.P1572T; 9:115048398-115048398 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2039A>G; p.Q680R; 9:115084301-115084301 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2039A>G; p.Q680R; 9:115084301-115084301 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.3760G>T; p.E1254*; 9:115063796-115063796 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1435C>T; p.R479C; 9:115086296-115086296 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.199G>A; p.D67N; 9:115090820-115090820 |
skin | malignant_melanoma | Substitution - Missense |
c.2039A>G; p.Q680R; 9:115084301-115084301 |
thyroid | other; neoplasm | Substitution - Missense |
c.2305C>T; p.R769W; 9:115081871-115081871 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.4727C>T; p.T1576I; 9:115048385-115048385 |
liver | carcinoma | Substitution - Missense |
c.4477G>A; p.A1493T; 9:115057255-115057255 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1298A>G; p.D433G; 9:115086433-115086433 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.4607C>T; p.T1536I; 9:115048505-115048505 |
skin | malignant_melanoma | Substitution - Missense |
c.2676C>T; p.G892G; 9:115076574-115076574 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2657A>T; p.K886I; 9:115077960-115077960 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.4607C>T; p.T1536I; 9:115048505-115048505 |
skin | malignant_melanoma | Substitution - Missense |
c.3088C>T; p.Q1030*; 9:115073729-115073729 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Nonsense |
c.3593A>G; p.Q1198R; 9:115063963-115063963 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2531G>T; p.G844V; 9:115078086-115078086 |
breast | carcinoma | Substitution - Missense |
c.3872A>G; p.Q1291R; 9:115063078-115063078 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3032A>G; p.K1011R; 9:115073785-115073785 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2684C>T; p.A895V; 9:115076566-115076566 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3066C>A; p.P1022P; 9:115073751-115073751 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.897C>T; p.C299C; 9:115086834-115086834 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.280G>T; p.G94W; 9:115090739-115090739 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.5113A>G; p.I1705V; 9:115046422-115046422 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.5331C>T; p.V1777V; 9:115041002-115041002 |
pancreas | carcinoma | Substitution - coding silent |
c.2134T>C; p.L712L; 9:115082805-115082805 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.529G>A; p.E177K; 9:115087202-115087202 |
skin | malignant_melanoma | Substitution - Missense |
c.2515A>T; p.I839F; 9:115078102-115078102 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.5074G>T; p.G1692*; 9:115046461-115046461 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.3958A>C; p.T1320P; 9:115062992-115062992 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1038C>T; p.C346C; 9:115086693-115086693 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2307G>A; p.R769R; 9:115081869-115081869 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.2137C>T; p.P713S; 9:115082802-115082802 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.4927G>A; p.D1643N; 9:115046608-115046608 |
skin | malignant_melanoma | Substitution - Missense |
c.780C>T; p.H260H; 9:115086951-115086951 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4857C>T; p.A1619A; 9:115046678-115046678 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.6600G>A; p.R2200R; 9:115021163-115021163 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2490C>T; p.I830I; 9:115078127-115078127 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2822C>A; p.P941Q; 9:115076428-115076428 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2490C>T; p.I830I; 9:115078127-115078127 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2490C>T; p.I830I; 9:115078127-115078127 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.5888G>T; p.R1963M; 9:115031585-115031585 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.5888G>T; p.R1963M; 9:115031585-115031585 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.219G>A; p.G73G; 9:115090800-115090800 |
skin | malignant_melanoma | Substitution - coding silent |
c.5888G>T; p.R1963M; 9:115031585-115031585 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.6293G>A; p.R2098H; 9:115026572-115026572 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.522T>G; p.C174W; 9:115087209-115087209 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Missense |
c.5888G>T; p.R1963M; 9:115031585-115031585 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2822C>A; p.P941Q; 9:115076428-115076428 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2822C>A; p.P941Q; 9:115076428-115076428 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.2616C>G; p.S872S; 9:115078001-115078001 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3925C>T; p.R1309C; 9:115063025-115063025 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3046C>T; p.R1016C; 9:115073771-115073771 |
skin | malignant_melanoma | Substitution - Missense |
c.2405-9C>T; p.?; 9:115078221-115078221 |
kidney | other; neoplasm | Unknown |
c.3925C>T; p.R1309C; 9:115063025-115063025 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3925C>T; p.R1309C; 9:115063025-115063025 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.3733A>T; p.T1245S; 9:115063823-115063823 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.6598C>T; p.R2200W; 9:115021165-115021165 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.370A>T; p.S124C; 9:115090649-115090649 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.5345T>C; p.M1782T; 9:115040988-115040988 |
breast | carcinoma | Substitution - Missense |
c.6332-8T>C; p.?; 9:115024144-115024144 |
liver | carcinoma; hepatocellular_carcinoma | Unknown |
c.6G>A; p.G2G; 9:115091013-115091013 |
skin | malignant_melanoma | Substitution - coding silent |
c.6332-8T>C; p.?; 9:115024144-115024144 |
liver | carcinoma | Unknown |
c.1303A>C; p.S435R; 9:115086428-115086428 |
stomach | carcinoma; mixed_intestinal_and_diffuse_adenocarcinoma-unclassifiable | Substitution - Missense |
c.3984C>T; p.G1328G; 9:115062966-115062966 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2119A>G; p.R707G; 9:115084221-115084221 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.5479G>T; p.D1827Y; 9:115038294-115038294 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.4204G>T; p.V1402L; 9:115059832-115059832 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.1342C>T; p.R448C; 9:115086389-115086389 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.3929C>T; p.S1310F; 9:115063021-115063021 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3193G>A; p.A1065T; 9:115073624-115073624 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3193G>A; p.A1065T; 9:115073624-115073624 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1411C>T; p.P471S; 9:115086320-115086320 |
kidney | other; neoplasm | Substitution - Missense |
c.1411C>T; p.P471S; 9:115086320-115086320 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.2412T>C; p.D804D; 9:115078205-115078205 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3028G>A; p.A1010T; 9:115073789-115073789 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2240G>C; p.R747P; 9:115082699-115082699 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - Missense |
c.1276_1277insTG; p.D426fs*44; 9:115086454-115086455 |
large_intestine; caecum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.146T>C; p.V49A; 9:115090873-115090873 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2675G>A; p.G892D; 9:115076575-115076575 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.2698C>T; p.R900*; 9:115076552-115076552 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.3834G>A; p.T1278T; 9:115063116-115063116 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3933G>A; p.M1311I; 9:115063017-115063017 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.5731delC; p.R1911fs*35; 9:115035260-115035260 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1641C>T; p.C547C; 9:115086090-115086090 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.363G>A; p.E121E; 9:115090656-115090656 |
skin | malignant_melanoma | Substitution - coding silent |
c.2513G>A; p.G838D; 9:115078104-115078104 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1280A>C; p.E427A; 9:115086451-115086451 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3453T>C; p.Y1151Y; 9:115064681-115064681 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2908G>A; p.E970K; 9:115076074-115076074 |
skin; neck | malignant_melanoma | Substitution - Missense |
c.490C>T; p.R164W; 9:115087241-115087241 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2537G>A; p.R846H; 9:115078080-115078080 |
skin | malignant_melanoma | Substitution - Missense |
c.5275G>A; p.G1759R; 9:115041058-115041058 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.5058C>T; p.Y1686Y; 9:115046477-115046477 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.5058C>T; p.Y1686Y; 9:115046477-115046477 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.124C>A; p.P42T; 9:115090895-115090895 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.5058C>T; p.Y1686Y; 9:115046477-115046477 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3215-1G>T; p.?; 9:115064920-115064920 |
large_intestine; caecum | carcinoma; adenocarcinoma | Unknown |
c.1249C>G; p.R417G; 9:115086482-115086482 |
skin | malignant_melanoma | Substitution - Missense |
c.2428G>T; p.E810*; 9:115078189-115078189 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.4615G>A; p.D1539N; 9:115048497-115048497 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3470C>T; p.S1157F; 9:115064664-115064664 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1105G>A; p.G369S; 9:115086626-115086626 |
skin | malignant_melanoma | Substitution - Missense |
c.329C>A; p.A110D; 9:115090690-115090690 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.3470C>T; p.S1157F; 9:115064664-115064664 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.590G>A; p.R197Q; 9:115087141-115087141 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2428G>T; p.E810*; 9:115078189-115078189 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - Nonsense |
c.3435T>G; p.Y1145*; 9:115064699-115064699 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1242C>T; p.G414G; 9:115086489-115086489 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2747G>A; p.G916D; 9:115076503-115076503 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.866A>C; p.Y289S; 9:115086865-115086865 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1570G>A; p.G524S; 9:115086161-115086161 |
liver | carcinoma | Substitution - Missense |
c.1570G>A; p.G524S; 9:115086161-115086161 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1065G>A; p.R355R; 9:115086666-115086666 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2280C>T; p.S760S; 9:115081896-115081896 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3328G>A; p.E1110K; 9:115064806-115064806 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1570G>A; p.G524S; 9:115086161-115086161 |
liver | carcinoma | Substitution - Missense |
c.5571C>T; p.L1857L; 9:115036183-115036183 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4460C>T; p.S1487F; 9:115057272-115057272 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.6110A>C; p.Y2037S; 9:115029419-115029419 |
thyroid | other; neoplasm | Substitution - Missense |
c.2427C>A; p.I809I; 9:115078190-115078190 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2333A>C; p.E778A; 9:115081843-115081843 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.5879G>A; p.G1960E; 9:115031594-115031594 |
skin; sole | malignant_melanoma; acral_lentiginous | Substitution - Missense |
c.6211G>A; p.E2071K; 9:115026654-115026654 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.932G>C; p.S311T; 9:115086799-115086799 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.4863G>A; p.P1621P; 9:115046672-115046672 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5320G>A; p.E1774K; 9:115041013-115041013 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3760G>A; p.E1254K; 9:115063796-115063796 |
skin | malignant_melanoma | Substitution - Missense |
c.6094G>A; p.G2032R; 9:115029435-115029435 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.5326C>A; p.L1776I; 9:115041007-115041007 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3347C>T; p.A1116V; 9:115064787-115064787 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3250G>C; p.E1084Q; 9:115064884-115064884 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.458-2A>G; p.?; 9:115087275-115087275 |
skin | malignant_melanoma | Unknown |
c.60C>T; p.T20T; 9:115090959-115090959 |
pancreas | carcinoma | Substitution - coding silent |
c.760G>T; p.V254L; 9:115086971-115086971 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.5133C>T; p.G1711G; 9:115042334-115042334 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4585C>T; p.L1529L; 9:115048527-115048527 |
skin | malignant_melanoma | Substitution - coding silent |
c.3286G>A; p.A1096T; 9:115064848-115064848 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.6601G>A; p.A2201T; 9:115021162-115021162 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.3168G>A; p.E1056E; 9:115073649-115073649 |
skin | malignant_melanoma | Substitution - coding silent |
c.4876C>A; p.L1626I; 9:115046659-115046659 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2675-1G>T; p.?; 9:115076576-115076576 |
large_intestine; caecum | carcinoma; adenocarcinoma | Unknown |
c.4876C>A; p.L1626I; 9:115046659-115046659 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.4876C>A; p.L1626I; 9:115046659-115046659 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.6339C>T; p.S2113S; 9:115024129-115024129 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4405A>G; p.T1469A; 9:115057327-115057327 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.179T>C; p.V60A; 9:115090840-115090840 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4697C>A; p.S1566Y; 9:115048415-115048415 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2218G>A; p.E740K; 9:115082721-115082721 |
skin | malignant_melanoma | Substitution - Missense |
c.6098G>T; p.R2033L; 9:115029431-115029431 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2374G>A; p.G792S; 9:115081802-115081802 |
skin | malignant_melanoma | Substitution - Missense |
c.5843C>A; p.S1948Y; 9:115031630-115031630 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2218G>A; p.E740K; 9:115082721-115082721 |
skin | malignant_melanoma | Substitution - Missense |
c.3597G>T; p.V1199V; 9:115063959-115063959 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1279G>A; p.E427K; 9:115086452-115086452 |
breast | carcinoma | Substitution - Missense |
c.5509A>G; p.K1837E; 9:115038264-115038264 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.4964G>T; p.R1655I; 9:115046571-115046571 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1964T>C; p.V655A; 9:115084376-115084376 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.3413C>T; p.T1138M; 9:115064721-115064721 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.969C>T; p.G323G; 9:115086762-115086762 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.47T>G; p.L16R; 9:115090972-115090972 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.343G>A; p.A115T; 9:115090676-115090676 |
pancreas | carcinoma | Substitution - Missense |
c.964C>T; p.R322W; 9:115086767-115086767 |
pancreas | carcinoma | Substitution - Missense |
c.964C>T; p.R322W; 9:115086767-115086767 |
pancreas | carcinoma; ductal_carcinoma | Substitution - Missense |
c.2607C>T; p.Y869Y; 9:115078010-115078010 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.102G>A; p.Q34Q; 9:115090917-115090917 |
skin | malignant_melanoma | Substitution - coding silent |
c.4710G>C; p.L1570L; 9:115048402-115048402 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.4472G>A; p.R1491Q; 9:115057260-115057260 |
NS | malignant_melanoma | Substitution - Missense |
c.5746G>A; p.G1916S; 9:115035245-115035245 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.4743G>A; p.Q1581Q; 9:115048369-115048369 |
skin | malignant_melanoma | Substitution - coding silent |
c.4922C>A; p.T1641K; 9:115046613-115046613 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.565G>A; p.E189K; 9:115087166-115087166 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.6260A>G; p.Y2087C; 9:115026605-115026605 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.561G>A; p.E187E; 9:115087170-115087170 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5638A>G; p.T1880A; 9:115036116-115036116 |
stomach | adenocarcinoma | Substitution - Missense |
c.5739A>C; p.S1913S; 9:115035252-115035252 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3536A>G; p.D1179G; 9:115064020-115064020 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.6424G>A; p.G2142R; 9:115024044-115024044 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1495C>T; p.R499C; 9:115086236-115086236 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.890A>G; p.N297S; 9:115086841-115086841 |
breast | carcinoma; ductal_carcinoma | Substitution - Missense |
c.5393C>A; p.A1798D; 9:115038380-115038380 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.226G>T; p.D76Y; 9:115090793-115090793 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.4081G>T; p.D1361Y; 9:115059955-115059955 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - Missense |
c.4427A>G; p.N1476S; 9:115057305-115057305 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.2830C>A; p.Q944K; 9:115076420-115076420 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.5478G>A; p.V1826V; 9:115038295-115038295 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2232C>A; p.I744I; 9:115082707-115082707 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.877C>T; p.R293*; 9:115086854-115086854 |
prostate | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.5992T>G; p.Y1998D; 9:115030334-115030334 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Missense |
c.1150C>T; p.R384C; 9:115086581-115086581 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2100G>T; p.K700N; 9:115084240-115084240 |
ovary | other; neoplasm | Substitution - Missense |
c.6187A>C; p.K2063Q; 9:115026678-115026678 |
thyroid | other; neoplasm | Substitution - Missense |
c.1496G>A; p.R499H; 9:115086235-115086235 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.5611A>G; p.K1871E; 9:115036143-115036143 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.126A>G; p.P42P; 9:115090893-115090893 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.6120G>A; p.W2040*; 9:115029409-115029409 |
skin | malignant_melanoma | Substitution - Nonsense |
c.451G>A; p.A151T; 9:115090568-115090568 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.45C>T; p.F15F; 9:115090974-115090974 |
skin | malignant_melanoma | Substitution - coding silent |
c.5889G>A; p.R1963R; 9:115031584-115031584 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.878G>A; p.R293Q; 9:115086853-115086853 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3539C>T; p.A1180V; 9:115064017-115064017 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2217T>C; p.F739F; 9:115082722-115082722 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.437G>T; p.C146F; 9:115090582-115090582 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.6444C>T; p.N2148N; 9:115024024-115024024 |
skin | malignant_melanoma | Substitution - coding silent |
c.3920G>C; p.S1307T; 9:115063030-115063030 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2030C>T; p.T677I; 9:115084310-115084310 |
skin | malignant_melanoma | Substitution - Missense |
c.3027G>A; p.L1009L; 9:115073790-115073790 |
skin | malignant_melanoma | Substitution - coding silent |
c.2741G>A; p.R914K; 9:115076509-115076509 |
skin | malignant_melanoma | Substitution - Missense |
c.4643C>T; p.S1548F; 9:115048469-115048469 |
skin | malignant_melanoma | Substitution - Missense |
c.5787+1G>A; p.?; 9:115035203-115035203 |
skin | malignant_melanoma | Unknown |
c.4643C>T; p.S1548F; 9:115048469-115048469 |
skin | malignant_melanoma | Substitution - Missense |
c.5059G>A; p.E1687K; 9:115046476-115046476 |
breast | carcinoma | Substitution - Missense |
c.847_848delCT; p.L283fs*15; 9:115086883-115086884 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Deletion - Frameshift |
c.5340C>T; p.I1780I; 9:115040993-115040993 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2940C>G; p.N980K; 9:115076042-115076042 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.922G>A; p.E308K; 9:115086809-115086809 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2940C>G; p.N980K; 9:115076042-115076042 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2797G>T; p.G933W; 9:115076453-115076453 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.5287C>T; p.Q1763*; 9:115041046-115041046 |
pancreas | carcinoma | Substitution - Nonsense |
c.4492C>A; p.L1498I; 9:115057240-115057240 |
large_intestine; colon | NS | Substitution - Missense |
c.4026C>T; p.V1342V; 9:115062924-115062924 |
breast | carcinoma | Substitution - coding silent |
c.4026C>T; p.V1342V; 9:115062924-115062924 |
prostate | carcinoma | Substitution - coding silent |
c.118A>G; p.T40A; 9:115090901-115090901 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.5053G>T; p.E1685*; 9:115046482-115046482 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.81A>T; p.K27N; 9:115090938-115090938 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3166G>A; p.E1056K; 9:115073651-115073651 |
skin | malignant_melanoma | Substitution - Missense |
c.1392C>A; p.D464E; 9:115086339-115086339 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.66T>G; p.G22G; 9:115090953-115090953 |
breast | carcinoma | Substitution - coding silent |
c.4351C>T; p.P1451S; 9:115057381-115057381 |
skin | malignant_melanoma | Substitution - Missense |
c.3459A>C; p.T1153T; 9:115064675-115064675 |
breast | carcinoma | Substitution - coding silent |
c.6394G>A; p.A2132T; 9:115024074-115024074 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.6114A>G; p.Q2038Q; 9:115029415-115029415 |
thyroid | other; neoplasm | Substitution - coding silent |
c.458-1G>A; p.?; 9:115087274-115087274 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.2609A>G; p.E870G; 9:115078008-115078008 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2609A>G; p.E870G; 9:115078008-115078008 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.829G>A; p.D277N; 9:115086902-115086902 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3243C>T; p.T1081T; 9:115064891-115064891 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.891T>C; p.N297N; 9:115086840-115086840 |
pancreas | carcinoma | Substitution - coding silent |
c.891T>C; p.N297N; 9:115086840-115086840 |
pancreas | carcinoma | Substitution - coding silent |
c.1103C>T; p.A368V; 9:115086628-115086628 |
skin | malignant_melanoma | Substitution - Missense |
c.4897C>A; p.P1633T; 9:115046638-115046638 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.891T>C; p.N297N; 9:115086840-115086840 |
pancreas | carcinoma | Substitution - coding silent |
c.5359G>A; p.E1787K; 9:115040974-115040974 |
skin | malignant_melanoma | Substitution - Missense |
c.2524G>A; p.V842M; 9:115078093-115078093 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.5217C>A; p.S1739R; 9:115042250-115042250 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.6451C>T; p.R2151C; 9:115024017-115024017 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.5359G>A; p.E1787K; 9:115040974-115040974 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3640C>T; p.P1214S; 9:115063916-115063916 |
skin | malignant_melanoma | Substitution - Missense |
c.3640C>T; p.P1214S; 9:115063916-115063916 |
skin | malignant_melanoma | Substitution - Missense |
c.1432G>A; p.G478S; 9:115086299-115086299 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.4617C>T; p.D1539D; 9:115048495-115048495 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.4617C>T; p.D1539D; 9:115048495-115048495 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.5337C>A; p.I1779I; 9:115040996-115040996 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.3634A>G; p.T1212A; 9:115063922-115063922 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1545G>C; p.Q515H; 9:115086186-115086186 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1697A>G; p.D566G; 9:115086034-115086034 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1621C>T; p.R541C; 9:115086110-115086110 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3047G>A; p.R1016H; 9:115073770-115073770 |
breast | carcinoma | Substitution - Missense |
c.3562C>A; p.P1188T; 9:115063994-115063994 |
skin | malignant_melanoma | Substitution - Missense |
c.564C>T; p.P188P; 9:115087167-115087167 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5768C>T; p.S1923L; 9:115035223-115035223 |
skin | malignant_melanoma | Substitution - Missense |
c.236C>T; p.P79L; 9:115090783-115090783 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.5586A>G; p.E1862E; 9:115036168-115036168 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.5153T>C; p.F1718S; 9:115042314-115042314 |
liver | carcinoma | Substitution - Missense |
c.4910G>A; p.R1637H; 9:115046625-115046625 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2848A>G; p.T950A; 9:115076402-115076402 |
breast | carcinoma | Substitution - Missense |
c.3564A>G; p.P1188P; 9:115063992-115063992 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2240G>T; p.R747L; 9:115082699-115082699 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.635C>T; p.T212M; 9:115087096-115087096 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.4105G>A; p.A1369T; 9:115059931-115059931 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1657T>G; p.F553V; 9:115086074-115086074 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3908C>T; p.T1303M; 9:115063042-115063042 |
peritoneum; appendix | other; pseudomyxoma_peritonei | Substitution - Missense |
c.3779G>A; p.G1260E; 9:115063171-115063171 |
skin | malignant_melanoma | Substitution - Missense |
c.4320A>T; p.E1440D; 9:115057412-115057412 |
liver | carcinoma | Substitution - Missense |
c.1164A>G; p.V388V; 9:115086567-115086567 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2285G>A; p.R762K; 9:115081891-115081891 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3053A>G; p.N1018S; 9:115073764-115073764 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2004C>T; p.F668F; 9:115084336-115084336 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3232_3233GA>AT; p.E1078>?; 9:115064901-115064902 |
NS | malignant_melanoma | Complex |
c.6364T>A; p.F2122I; 9:115024104-115024104 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2004C>T; p.F668F; 9:115084336-115084336 |
skin | malignant_melanoma | Substitution - coding silent |
c.1976C>T; p.T659I; 9:115084364-115084364 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.5156C>T; p.S1719L; 9:115042311-115042311 |
skin | malignant_melanoma | Substitution - Missense |
c.809G>A; p.C270Y; 9:115086922-115086922 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2700A>G; p.R900R; 9:115076550-115076550 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2049G>A; p.E683E; 9:115084291-115084291 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.2212G>A; p.A738T; 9:115082727-115082727 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.6098G>A; p.R2033H; 9:115029431-115029431 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.6456C>T; p.V2152V; 9:115024012-115024012 |
skin | malignant_melanoma | Substitution - coding silent |
c.2049G>A; p.E683E; 9:115084291-115084291 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1489C>T; p.R497W; 9:115086242-115086242 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.5532G>A; p.T1844T; 9:115036222-115036222 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.6274G>A; p.V2092M; 9:115026591-115026591 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1063C>T; p.R355W; 9:115086668-115086668 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.6274G>A; p.V2092M; 9:115026591-115026591 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1477G>T; p.G493W; 9:115086254-115086254 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.6498C>T; p.G2166G; 9:115021265-115021265 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.6498C>T; p.G2166G; 9:115021265-115021265 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.250A>T; p.S84C; 9:115090769-115090769 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2947A>G; p.T983A; 9:115076035-115076035 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3478G>T; p.A1160S; 9:115064656-115064656 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.2173G>A; p.E725K; 9:115082766-115082766 |
skin | malignant_melanoma | Substitution - Missense |
c.5528G>A; p.R1843H; 9:115036226-115036226 |
breast | carcinoma | Substitution - Missense |
c.847C>T; p.L283L; 9:115086884-115086884 |
breast | carcinoma | Substitution - coding silent |
c.3543C>T; p.L1181L; 9:115064013-115064013 |
skin | malignant_melanoma | Substitution - coding silent |
c.4993G>A; p.E1665K; 9:115046542-115046542 |
skin | malignant_melanoma | Substitution - Missense |
c.2025G>A; p.T675T; 9:115084315-115084315 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.2372G>C; p.R791P; 9:115081804-115081804 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1992G>T; p.L664L; 9:115084348-115084348 |
skin | malignant_melanoma | Substitution - coding silent |
c.4370C>T; p.S1457F; 9:115057362-115057362 |
skin | malignant_melanoma | Substitution - Missense |
c.6218G>A; p.R2073Q; 9:115026647-115026647 |
large_intestine; colon | NS | Substitution - Missense |
c.2439T>G; p.D813E; 9:115078178-115078178 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.453C>T; p.A151A; 9:115090566-115090566 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1351G>A; p.E451K; 9:115086380-115086380 |
liver | carcinoma | Substitution - Missense |
c.1813delG; p.V605fs*27; 9:115085918-115085918 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Deletion - Frameshift |
c.114C>T; p.N38N; 9:115090905-115090905 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5583G>A; p.T1861T; 9:115036171-115036171 |
skin | malignant_melanoma | Substitution - coding silent |
c.2213C>T; p.A738V; 9:115082726-115082726 |
breast | carcinoma | Substitution - Missense |
c.5250T>C; p.G1750G; 9:115041083-115041083 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5608G>C; p.E1870Q; 9:115036146-115036146 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.4129T>G; p.F1377V; 9:115059907-115059907 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.6018G>T; p.K2006N; 9:115030308-115030308 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2191G>A; p.E731K; 9:115082748-115082748 |
skin | malignant_melanoma | Substitution - Missense |
c.2680G>A; p.D894N; 9:115076570-115076570 |
skin | malignant_melanoma | Substitution - Missense |
c.2942C>G; p.A981G; 9:115076040-115076040 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.2942C>G; p.A981G; 9:115076040-115076040 |
liver | carcinoma | Substitution - Missense |
c.2826G>C; p.K942N; 9:115076424-115076424 |
breast | carcinoma; HER-positive_carcinoma | Substitution - Missense |
c.1272G>A; p.V424V; 9:115086459-115086459 |
pancreas | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.1272G>A; p.V424V; 9:115086459-115086459 |
pancreas | carcinoma | Substitution - coding silent |
c.667A>C; p.S223R; 9:115087064-115087064 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.5013C>T; p.P1671P; 9:115046522-115046522 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4942G>A; p.D1648N; 9:115046593-115046593 |
ovary | other; neoplasm | Substitution - Missense |
c.457G>C; p.G153R; 9:115090562-115090562 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3303T>A; p.Y1101*; 9:115064831-115064831 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1177G>T; p.E393*; 9:115086554-115086554 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Nonsense |
c.1421G>A; p.C474Y; 9:115086310-115086310 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3320A>G; p.Q1107R; 9:115064814-115064814 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.6069G>A; p.W2023*; 9:115030257-115030257 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.6219G>A; p.R2073R; 9:115026646-115026646 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.348C>T; p.A116A; 9:115090671-115090671 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.4133T>C; p.V1378A; 9:115059903-115059903 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.5898G>A; p.M1966I; 9:115031575-115031575 |
skin; trunk | malignant_melanoma | Substitution - Missense |
c.2905A>C; p.K969Q; 9:115076077-115076077 |
breast | carcinoma | Substitution - Missense |
c.92A>G; p.H31R; 9:115090927-115090927 |
liver | carcinoma | Substitution - Missense |
c.237G>A; p.P79P; 9:115090782-115090782 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.237G>A; p.P79P; 9:115090782-115090782 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5278A>G; p.T1760A; 9:115041055-115041055 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2562C>T; p.D854D; 9:115078055-115078055 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2523C>T; p.D841D; 9:115078094-115078094 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5148C>T; p.V1716V; 9:115042319-115042319 |
breast | carcinoma | Substitution - coding silent |
c.1350C>T; p.V450V; 9:115086381-115086381 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5996C>G; p.T1999S; 9:115030330-115030330 |
skin | malignant_melanoma | Substitution - Missense |
c.4575G>A; p.T1525T; 9:115057157-115057157 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4571C>T; p.A1524V; 9:115057161-115057161 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1987G>C; p.G663R; 9:115084353-115084353 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.6432C>T; p.F2144F; 9:115024036-115024036 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.4496C>G; p.P1499R; 9:115057236-115057236 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.2215T>G; p.F739V; 9:115082724-115082724 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.347C>T; p.A116V; 9:115090672-115090672 |
pancreas | carcinoma | Substitution - Missense |
c.347C>T; p.A116V; 9:115090672-115090672 |
pancreas | carcinoma | Substitution - Missense |
c.4788G>T; p.E1596D; 9:115048324-115048324 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.746G>A; p.R249H; 9:115086985-115086985 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.4460C>A; p.S1487Y; 9:115057272-115057272 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.5067A>C; p.E1689D; 9:115046468-115046468 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2865G>A; p.L955L; 9:115076117-115076117 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.456A>G; p.T152T; 9:115090563-115090563 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2323C>T; p.P775S; 9:115081853-115081853 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.6043G>T; p.D2015Y; 9:115030283-115030283 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2323C>T; p.P775S; 9:115081853-115081853 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.6294C>T; p.R2098R; 9:115026571-115026571 |
skin | malignant_melanoma | Substitution - coding silent |
c.6331G>T; p.G2111C; 9:115026534-115026534 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4833G>C; p.L1611F; 9:115048279-115048279 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.5222G>A; p.R1741Q; 9:115042245-115042245 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.5222G>A; p.R1741Q; 9:115042245-115042245 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.3247A>G; p.T1083A; 9:115064887-115064887 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1868-2A>G; p.?; 9:115084474-115084474 |
lung | carcinoma; squamous_cell_carcinoma | Unknown |
c.5174C>T; p.S1725L; 9:115042293-115042293 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.528C>T; p.C176C; 9:115087203-115087203 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.5174C>T; p.S1725L; 9:115042293-115042293 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.6093C>T; p.N2031N; 9:115029436-115029436 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.528C>T; p.C176C; 9:115087203-115087203 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1904C>T; p.T635M; 9:115084436-115084436 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.4941C>T; p.F1647F; 9:115046594-115046594 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3673C>T; p.L1225F; 9:115063883-115063883 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.3673C>T; p.L1225F; 9:115063883-115063883 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.4941C>T; p.F1647F; 9:115046594-115046594 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3724T>G; p.F1242V; 9:115063832-115063832 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1723G>T; p.D575Y; 9:115086008-115086008 |
liver | carcinoma | Substitution - Missense |
c.1337G>A; p.R446Q; 9:115086394-115086394 |
prostate | carcinoma | Substitution - Missense |
c.5020A>G; p.T1674A; 9:115046515-115046515 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.5252C>T; p.T1751I; 9:115041081-115041081 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1723G>T; p.D575Y; 9:115086008-115086008 |
liver | carcinoma | Substitution - Missense |
c.4686G>C; p.T1562T; 9:115048426-115048426 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.6083G>A; p.R2028K; 9:115029446-115029446 |
skin | malignant_melanoma | Substitution - Missense |
c.471C>A; p.T157T; 9:115087260-115087260 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1479G>A; p.G493G; 9:115086252-115086252 |
skin | malignant_melanoma | Substitution - coding silent |
c.1232G>A; p.G411D; 9:115086499-115086499 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3868G>A; p.V1290I; 9:115063082-115063082 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.5852A>G; p.Y1951C; 9:115031621-115031621 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1342C>G; p.R448G; 9:115086389-115086389 |
pancreas | carcinoma; adenocarcinoma | Substitution - Missense |
c.5881C>T; p.P1961S; 9:115031592-115031592 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1826G>A; p.C609Y; 9:115085905-115085905 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.5527C>T; p.R1843C; 9:115036227-115036227 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3764A>G; p.E1255G; 9:115063186-115063186 |
breast | carcinoma | Substitution - Missense |
c.2214T>C; p.A738A; 9:115082725-115082725 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.997G>A; p.E333K; 9:115086734-115086734 |
skin | malignant_melanoma | Substitution - Missense |
c.2214T>C; p.A738A; 9:115082725-115082725 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4590C>T; p.P1530P; 9:115048522-115048522 |
skin | malignant_melanoma | Substitution - coding silent |
c.4383C>T; p.T1461T; 9:115057349-115057349 |
skin | malignant_melanoma | Substitution - coding silent |
c.1950A>T; p.T650T; 9:115084390-115084390 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1936G>A; p.E646K; 9:115084404-115084404 |
skin | malignant_melanoma | Substitution - Missense |
c.5604T>A; p.F1868L; 9:115036150-115036150 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2792C>T; p.S931F; 9:115076458-115076458 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.991T>G; p.Y331D; 9:115086740-115086740 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.3918C>T; p.G1306G; 9:115063032-115063032 |
breast | carcinoma | Substitution - coding silent |
c.3765G>T; p.E1255D; 9:115063185-115063185 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.5530A>G; p.T1844A; 9:115036224-115036224 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3765G>T; p.E1255D; 9:115063185-115063185 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.5343C>T; p.A1781A; 9:115040990-115040990 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.4902C>G; p.D1634E; 9:115046633-115046633 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3414G>A; p.T1138T; 9:115064720-115064720 |
pancreas | carcinoma | Substitution - coding silent |
c.2047G>A; p.E683K; 9:115084293-115084293 |
NS | malignant_melanoma | Substitution - Missense |
c.5673A>G; p.R1891R; 9:115035318-115035318 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3760+1G>A; p.?; 9:115063795-115063795 |
large_intestine; colon | adenoma | Unknown |
c.2019C>G; p.D673E; 9:115084321-115084321 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3356A>T; p.N1119I; 9:115064778-115064778 |
liver | carcinoma | Substitution - Missense |
c.3356A>T; p.N1119I; 9:115064778-115064778 |
liver | carcinoma | Substitution - Missense |
c.3482C>T; p.S1161F; 9:115064652-115064652 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3155T>C; p.L1052P; 9:115073662-115073662 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.520T>G; p.C174G; 9:115087211-115087211 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1743C>G; p.H581Q; 9:115085988-115085988 |
ovary | other; neoplasm | Substitution - Missense |
c.3529G>C; p.G1177R; 9:115064027-115064027 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.4735G>A; p.G1579R; 9:115048377-115048377 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1926C>T; p.A642A; 9:115084414-115084414 |
skin | malignant_melanoma | Substitution - coding silent |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
thyroid | other; neoplasm | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.427G>T; p.G143*; 9:115090592-115090592 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2833C>A; p.Q945K; 9:115076417-115076417 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.6511C>A; p.H2171N; 9:115021252-115021252 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.276G>A; p.V92V; 9:115090743-115090743 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.589C>T; p.R197*; 9:115087142-115087142 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.627C>T; p.D209D; 9:115087104-115087104 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.589C>T; p.R197*; 9:115087142-115087142 |
skin | malignant_melanoma | Substitution - Nonsense |
c.276G>A; p.V92V; 9:115090743-115090743 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.589C>T; p.R197*; 9:115087142-115087142 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1053C>T; p.H351H; 9:115086678-115086678 |
breast | carcinoma | Substitution - coding silent |
c.276G>A; p.V92V; 9:115090743-115090743 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.589C>T; p.R197*; 9:115087142-115087142 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2440G>T; p.V814F; 9:115078177-115078177 |
prostate | carcinoma | Substitution - Missense |
c.5029A>T; p.I1677L; 9:115046506-115046506 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.4814G>A; p.G1605E; 9:115048298-115048298 |
skin | malignant_melanoma | Substitution - Missense |
c.5129T>C; p.M1710T; 9:115042338-115042338 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.5350G>A; p.G1784S; 9:115040983-115040983 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2916G>T; p.K972N; 9:115076066-115076066 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.5129T>C; p.M1710T; 9:115042338-115042338 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.5677T>G; p.L1893V; 9:115035314-115035314 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.3227A>G; p.E1076G; 9:115064907-115064907 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.5247A>G; p.G1749G; 9:115042220-115042220 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1932C>A; p.D644E; 9:115084408-115084408 |
skin; ear | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.194C>T; p.S65L; 9:115090825-115090825 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2679C>T; p.L893L; 9:115076571-115076571 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.194C>T; p.S65L; 9:115090825-115090825 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2679C>T; p.L893L; 9:115076571-115076571 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5166T>C; p.T1722T; 9:115042301-115042301 |
liver | carcinoma | Substitution - coding silent |
c.1837G>A; p.E613K; 9:115085894-115085894 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1488C>T; p.C496C; 9:115086243-115086243 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5505C>T; p.G1835G; 9:115038268-115038268 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |