General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 29119 |
Name | CTNNA3 |
Synonymous | catenin (cadherin-associated protein), alpha 3;CTNNA3;catenin (cadherin-associated protein), alpha 3 |
Definition | alpha-T-catenin|alpha-catenin-like protein|catenin alpha-3 |
Position | 10q22.2 |
Gene Type | protein-coding |
Mutation summary: | Mutations in domains Mutational pattern in 17 major cancer types LoF vs missense mutations All the copy number variations from COSMIC database V72 All the mutations from COSMIC database V72 |
Mutation summary in protein domains | Top |
The non-synonymous (top) and synonymous (bottom) mutational percentage for various cancers | Top |
Loss of Function mutations compare to missense mutations | Top |
The ratio of the loss-of-function mutations over missense mutations is 0.13. |
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.1896A>G; p.E632E; 10:66103238-66103238 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.616G>A; p.G206R; 10:67219834-67219834 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2160-2A>G; p.?; 10:65988799-65988799 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.1839C>A; p.I613I; 10:66280515-66280515 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2546G>C; p.R849T; 10:65920472-65920472 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1582C>A; p.Q528K; 10:66379302-66379302 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1382A>G; p.N461S; 10:66520766-66520766 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.687T>C; p.S229S; 10:67219763-67219763 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1443G>T; p.M481I; 10:66520705-66520705 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.2249G>A; p.R750Q; 10:65988708-65988708 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2546G>C; p.R849T; 10:65920472-65920472 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - Missense |
c.1813C>T; p.Q605*; 10:66280541-66280541 |
skin; upper_arm | malignant_melanoma | Substitution - Nonsense |
c.129C>T; p.N43N; 10:67607020-67607020 |
skin | malignant_melanoma | Substitution - coding silent |
c.778C>T; p.Q260*; 10:67219672-67219672 |
urinary_tract; bladder | carcinoma | Substitution - Nonsense |
c.2487A>C; p.S829S; 10:65920531-65920531 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.82G>A; p.E28K; 10:67647432-67647432 |
skin | malignant_melanoma | Substitution - Missense |
c.2153T>C; p.F718S; 10:66069314-66069314 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1000G>A; p.A334T; 10:67180364-67180364 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1390C>A; p.L464I; 10:66520758-66520758 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1000G>A; p.A334T; 10:67180364-67180364 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.991G>A; p.E331K; 10:67180373-67180373 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1775C>A; p.A592D; 10:66280579-66280579 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1222G>A; p.E408K; 10:66766323-66766323 |
skin | malignant_melanoma | Substitution - Missense |
c.950C>T; p.S317F; 10:67180414-67180414 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.34G>A; p.D12N; 10:67647480-67647480 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1007G>A; p.R336H; 10:67180357-67180357 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.182C>T; p.S61F; 10:67606967-67606967 |
skin; face | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1222G>A; p.E408K; 10:66766323-66766323 |
skin | malignant_melanoma | Substitution - Missense |
c.2520G>A; p.G840G; 10:65920498-65920498 |
stomach | adenocarcinoma | Substitution - coding silent |
c.2520G>A; p.G840G; 10:65920498-65920498 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2569C>A; p.P857T; 10:65920449-65920449 |
oesophagus | carcinoma | Substitution - Missense |
c.650T>A; p.L217H; 10:67219800-67219800 |
breast | carcinoma | Substitution - Missense |
c.582C>A; p.D194E; 10:67219868-67219868 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1604G>A; p.R535H; 10:66379280-66379280 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1333G>A; p.V445I; 10:66621733-66621733 |
skin | malignant_melanoma | Substitution - Missense |
c.2565A>C; p.K855N; 10:65920453-65920453 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.64A>C; p.T22P; 10:67647450-67647450 |
breast | carcinoma | Substitution - Missense |
c.1033G>A; p.E345K; 10:67180331-67180331 |
skin | malignant_melanoma | Substitution - Missense |
c.1451G>A; p.R484H; 10:66520697-66520697 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.105C>G; p.T35T; 10:67607044-67607044 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1451G>A; p.R484H; 10:66520697-66520697 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.437G>T; p.C146F; 10:67539525-67539525 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1528T>A; p.S510T; 10:66520620-66520620 |
fallopian_tube | carcinoma; serous_carcinoma | Substitution - Missense |
c.1964G>A; p.G655E; 10:66103170-66103170 |
skin | malignant_melanoma | Substitution - Missense |
c.1848A>G; p.T616T; 10:66280506-66280506 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2337G>A; p.L779L; 10:65966675-65966675 |
skin | malignant_melanoma | Substitution - coding silent |
c.1964G>A; p.G655E; 10:66103170-66103170 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1964G>A; p.G655E; 10:66103170-66103170 |
skin | malignant_melanoma | Substitution - Missense |
c.2435A>C; p.K812T; 10:65920583-65920583 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1989T>C; p.T663T; 10:66069478-66069478 |
oesophagus | carcinoma | Substitution - coding silent |
c.1585G>A; p.D529N; 10:66379299-66379299 |
skin | malignant_melanoma | Substitution - Missense |
c.2490delC; p.K831fs*16; 10:65920528-65920528 |
lung | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2435A>C; p.K812T; 10:65920583-65920583 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - Missense |
c.1021G>A; p.D341N; 10:67180343-67180343 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.686C>T; p.S229F; 10:67219764-67219764 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1360A>C; p.T454P; 10:66621706-66621706 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.2472G>T; p.M824I; 10:65920546-65920546 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.161G>A; p.R54K; 10:67606988-67606988 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2378G>A; p.G793E; 10:65966634-65966634 |
skin | malignant_melanoma | Substitution - Missense |
c.2399C>T; p.A800V; 10:65966613-65966613 |
skin; trunk | malignant_melanoma | Substitution - Missense |
c.1930G>A; p.E644K; 10:66103204-66103204 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.346C>T; p.P116S; 10:67539616-67539616 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1183C>A; p.P395T; 10:66766362-66766362 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.544G>A; p.E182K; 10:67521877-67521877 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.346C>T; p.P116S; 10:67539616-67539616 |
skin | malignant_melanoma | Substitution - Missense |
c.1930G>A; p.E644K; 10:66103204-66103204 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1639G>C; p.V547L; 10:66379245-66379245 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1885-1G>A; p.?; 10:66103250-66103250 |
oesophagus | carcinoma; squamous_cell_carcinoma | Unknown |
c.1995G>T; p.L665L; 10:66069472-66069472 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1412A>T; p.K471I; 10:66520736-66520736 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1028T>C; p.L343P; 10:67180336-67180336 |
skin | malignant_melanoma | Substitution - Missense |
c.1885-1G>A; p.?; 10:66103250-66103250 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Unknown |
c.2136G>T; p.M712I; 10:66069331-66069331 |
breast | carcinoma | Substitution - Missense |
c.468G>A; p.R156R; 10:67521953-67521953 |
skin | malignant_melanoma | Substitution - coding silent |
c.1064G>T; p.R355M; 10:66775508-66775508 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2525G>T; p.R842L; 10:65920493-65920493 |
large_intestine | adenoma | Substitution - Missense |
c.1518C>T; p.F506F; 10:66520630-66520630 |
skin | malignant_melanoma | Substitution - coding silent |
c.2501G>A; p.R834Q; 10:65920517-65920517 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1655C>T; p.T552M; 10:66379229-66379229 |
pancreas | carcinoma | Substitution - Missense |
c.1271G>T; p.R424M; 10:66766274-66766274 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2386C>A; p.L796I; 10:65966626-65966626 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2608G>T; p.A870S; 10:65920410-65920410 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.2501G>A; p.R834Q; 10:65920517-65920517 |
skin | malignant_melanoma | Substitution - Missense |
c.1655C>T; p.T552M; 10:66379229-66379229 |
pancreas | carcinoma; ductal_carcinoma | Substitution - Missense |
c.1902G>A; p.E634E; 10:66103232-66103232 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; polycythaemia_vera | Substitution - coding silent |
c.807G>T; p.Q269H; 10:67219643-67219643 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2097C>T; p.N699N; 10:66069370-66069370 |
prostate | carcinoma | Substitution - coding silent |
c.892C>T; p.P298S; 10:67180472-67180472 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2133C>T; p.I711I; 10:66069334-66069334 |
skin | malignant_melanoma | Substitution - coding silent |
c.1161C>A; p.D387E; 10:66766384-66766384 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.1161C>A; p.D387E; 10:66766384-66766384 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.2133C>T; p.I711I; 10:66069334-66069334 |
skin | malignant_melanoma | Substitution - coding silent |
c.828C>T; p.A276A; 10:67219622-67219622 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1402G>T; p.A468S; 10:66520746-66520746 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2615G>T; p.R872I; 10:65920403-65920403 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1265C>T; p.T422I; 10:66766280-66766280 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1170G>T; p.L390L; 10:66766375-66766375 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.876T>C; p.T292T; 10:67180488-67180488 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1706G>A; p.R569K; 10:66379178-66379178 |
stomach | adenocarcinoma | Substitution - Missense |
c.835G>T; p.E279*; 10:67219615-67219615 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.563C>T; p.A188V; 10:67521858-67521858 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_T_cell_leukaemia | Substitution - Missense |
c.174T>C; p.L58L; 10:67606975-67606975 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1542C>A; p.I514I; 10:66379342-66379342 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1591G>A; p.D531N; 10:66379293-66379293 |
skin | malignant_melanoma | Substitution - Missense |
c.1594A>G; p.N532D; 10:66379290-66379290 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.960G>A; p.T320T; 10:67180404-67180404 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.960G>A; p.T320T; 10:67180404-67180404 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2600C>A; p.T867K; 10:65920418-65920418 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1059delA; p.E354fs*6; 10:66775513-66775513 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.973C>T; p.R325*; 10:67180391-67180391 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2115C>A; p.A705A; 10:66069352-66069352 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.1059delA; p.E354fs*6; 10:66775513-66775513 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1059delA; p.E354fs*6; 10:66775513-66775513 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.973C>T; p.R325*; 10:67180391-67180391 |
pancreas | carcinoma | Substitution - Nonsense |
c.2276C>T; p.P759L; 10:65966736-65966736 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1175C>T; p.T392M; 10:66766370-66766370 |
endometrium | carcinoma; serous_carcinoma | Substitution - Missense |
c.1175C>T; p.T392M; 10:66766370-66766370 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2205G>A; p.A735A; 10:65988752-65988752 |
skin | malignant_melanoma | Substitution - coding silent |
c.2205G>A; p.A735A; 10:65988752-65988752 |
liver | carcinoma | Substitution - coding silent |
c.38C>T; p.P13L; 10:67647476-67647476 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1963G>A; p.G655R; 10:66103171-66103171 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2205G>A; p.A735A; 10:65988752-65988752 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1997C>A; p.P666H; 10:66069470-66069470 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1094A>G; p.N365S; 10:66775478-66775478 |
breast | carcinoma | Substitution - Missense |
c.1465C>G; p.H489D; 10:66520683-66520683 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.37C>T; p.P13S; 10:67647477-67647477 |
skin | malignant_melanoma | Substitution - Missense |
c.2148A>C; p.T716T; 10:66069319-66069319 |
skin | malignant_melanoma | Substitution - coding silent |
c.2596G>A; p.E866K; 10:65920422-65920422 |
skin | malignant_melanoma | Substitution - Missense |
c.1918G>T; p.E640*; 10:66103216-66103216 |
adrenal_gland; adrenal_gland | adrenal_cortical_carcinoma; functioning | Substitution - Nonsense |
c.1789T>C; p.S597P; 10:66280565-66280565 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2167G>T; p.G723*; 10:65988790-65988790 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.1523C>T; p.A508V; 10:66520625-66520625 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.474T>G; p.F158L; 10:67521947-67521947 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.66C>T; p.T22T; 10:67647448-67647448 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1129-8C>A; p.?; 10:66766424-66766424 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Unknown |
c.2265G>A; p.Q755Q; 10:65988692-65988692 |
skin | malignant_melanoma | Substitution - coding silent |
c.2550G>A; p.M850I; 10:65920468-65920468 |
skin | malignant_melanoma | Substitution - Missense |
c.586A>G; p.K196E; 10:67219864-67219864 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2125T>C; p.C709R; 10:66069342-66069342 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2364G>A; p.E788E; 10:65966648-65966648 |
skin | malignant_melanoma | Substitution - coding silent |
c.1982A>C; p.K661T; 10:66069485-66069485 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2574G>T; p.L858F; 10:65920444-65920444 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1982A>C; p.K661T; 10:66069485-66069485 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2380G>A; p.G794R; 10:65966632-65966632 |
skin | malignant_melanoma | Substitution - Missense |
c.2031T>A; p.V677V; 10:66069436-66069436 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.398C>T; p.T133M; 10:67539564-67539564 |
pancreas | carcinoma | Substitution - Missense |
c.411C>T; p.I137I; 10:67539551-67539551 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1958C>A; p.T653N; 10:66103176-66103176 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.539A>T; p.E180V; 10:67521882-67521882 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1848A>C; p.T616T; 10:66280506-66280506 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1126C>T; p.Q376*; 10:66775446-66775446 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.284G>A; p.R95H; 10:67606865-67606865 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.284G>A; p.R95H; 10:67606865-67606865 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1538A>G; p.H513R; 10:66379346-66379346 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.284G>A; p.R95H; 10:67606865-67606865 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.284G>A; p.R95H; 10:67606865-67606865 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1126C>T; p.Q376*; 10:66775446-66775446 |
bone; pelvis | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Nonsense |
c.1089A>T; p.L363F; 10:66775483-66775483 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1374+2T>A; p.?; 10:66621690-66621690 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Unknown |
c.768A>C; p.S256S; 10:67219682-67219682 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1807G>A; p.D603N; 10:66280547-66280547 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2167G>A; p.G723R; 10:65988790-65988790 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.200G>A; p.W67*; 10:67606949-67606949 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.2500C>T; p.R834*; 10:65920518-65920518 |
prostate | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1272G>T; p.R424S; 10:66766273-66766273 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.156G>A; p.S52S; 10:67606993-67606993 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.156G>A; p.S52S; 10:67606993-67606993 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2006A>T; p.E669V; 10:66069461-66069461 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2059C>G; p.L687V; 10:66069408-66069408 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2040C>T; p.F680F; 10:66069427-66069427 |
skin | malignant_melanoma | Substitution - coding silent |
c.924C>T; p.I308I; 10:67180440-67180440 |
skin | malignant_melanoma | Substitution - coding silent |
c.924C>T; p.I308I; 10:67180440-67180440 |
skin | malignant_melanoma | Substitution - coding silent |
c.2246C>T; p.A749V; 10:65988711-65988711 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1345G>A; p.A449T; 10:66621721-66621721 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1052G>A; p.G351E; 10:66775520-66775520 |
skin | malignant_melanoma | Substitution - Missense |
c.999C>T; p.N333N; 10:67180365-67180365 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1650C>T; p.I550I; 10:66379234-66379234 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.312A>T; p.S104S; 10:67539650-67539650 |
breast | carcinoma | Substitution - coding silent |
c.1766C>G; p.A589G; 10:66280588-66280588 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1692_1693GG>TA; p.T564>?; 10:66379191-66379192 |
lung | carcinoma; adenocarcinoma | Complex |
c.1451G>T; p.R484L; 10:66520697-66520697 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1965G>A; p.G655G; 10:66103169-66103169 |
skin | malignant_melanoma | Substitution - coding silent |
c.1965G>A; p.G655G; 10:66103169-66103169 |
skin | malignant_melanoma | Substitution - coding silent |
c.1775C>T; p.A592V; 10:66280579-66280579 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1024C>A; p.L342M; 10:67180340-67180340 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.1628G>A; p.R543Q; 10:66379256-66379256 |
breast | carcinoma | Substitution - Missense |
c.1797T>G; p.N599K; 10:66280557-66280557 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.1628G>A; p.R543Q; 10:66379256-66379256 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1885-2A>C; p.?; 10:66103251-66103251 |
lung | carcinoma; squamous_cell_carcinoma | Unknown |
c.1822G>T; p.D608Y; 10:66280532-66280532 |
thyroid | other; neoplasm | Substitution - Missense |
c.2531C>A; p.P844Q; 10:65920487-65920487 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2114C>A; p.A705D; 10:66069353-66069353 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.67G>A; p.V23M; 10:67647447-67647447 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.67G>A; p.V23M; 10:67647447-67647447 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.67G>A; p.V23M; 10:67647447-67647447 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1052G>C; p.G351A; 10:66775520-66775520 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.889C>T; p.R297*; 10:67180475-67180475 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.889C>T; p.R297*; 10:67180475-67180475 |
ovary | carcinoma; serous_carcinoma | Substitution - Nonsense |
c.883G>A; p.E295K; 10:67180481-67180481 |
skin | malignant_melanoma | Substitution - Missense |
c.1421C>T; p.A474V; 10:66520727-66520727 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1186C>T; p.L396F; 10:66766359-66766359 |
skin | malignant_melanoma | Substitution - Missense |
c.1482T>C; p.T494T; 10:66520666-66520666 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.417G>A; p.A139A; 10:67539545-67539545 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.974G>A; p.R325Q; 10:67180390-67180390 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2575A>T; p.I859F; 10:65920443-65920443 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.974G>A; p.R325Q; 10:67180390-67180390 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1616C>T; p.A539V; 10:66379268-66379268 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.974G>A; p.R325Q; 10:67180390-67180390 |
skin | malignant_melanoma | Substitution - Missense |
c.2074G>A; p.E692K; 10:66069393-66069393 |
skin | malignant_melanoma | Substitution - Missense |
c.1978G>T; p.A660S; 10:66069489-66069489 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.483C>G; p.L161L; 10:67521938-67521938 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.842A>G; p.E281G; 10:67219608-67219608 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.38C>A; p.P13H; 10:67647476-67647476 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1237G>C; p.E413Q; 10:66766308-66766308 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.842A>G; p.E281G; 10:67219608-67219608 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2543G>A; p.W848*; 10:65920475-65920475 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.842A>G; p.E281G; 10:67219608-67219608 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2266-10T>G; p.?; 10:65966756-65966756 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.2266-10T>G; p.?; 10:65966756-65966756 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Unknown |
c.1241A>G; p.Y414C; 10:66766304-66766304 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2266-10T>G; p.?; 10:65966756-65966756 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Unknown |
c.1375-2A>G; p.?; 10:66520775-66520775 |
lung | carcinoma; squamous_cell_carcinoma | Unknown |
c.509T>G; p.L170R; 10:67521912-67521912 |
skin | malignant_melanoma | Substitution - Missense |
c.263C>T; p.T88M; 10:67606886-67606886 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1348A>C; p.N450H; 10:66621718-66621718 |
prostate | carcinoma | Substitution - Missense |
c.993A>T; p.E331D; 10:67180371-67180371 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1733-6T>C; p.?; 10:66280627-66280627 |
skin; head_neck | malignant_melanoma; superficial_spreading | Unknown |
c.1159G>A; p.D387N; 10:66766386-66766386 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1434C>T; p.T478T; 10:66520714-66520714 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1875G>C; p.M625I; 10:66280479-66280479 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.729A>T; p.E243D; 10:67219721-67219721 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.2307G>A; p.L769L; 10:65966705-65966705 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2345G>A; p.C782Y; 10:65966667-65966667 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.2266-1G>T; p.?; 10:65966747-65966747 |
lung | carcinoma; adenocarcinoma | Unknown |
c.2198A>T; p.Y733F; 10:65988759-65988759 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.1167C>T; p.F389F; 10:66766378-66766378 |
skin | malignant_melanoma | Substitution - coding silent |
c.394G>A; p.V132M; 10:67539568-67539568 |
skin | malignant_melanoma | Substitution - Missense |
c.42G>T; p.Q14H; 10:67647472-67647472 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.987C>T; p.I329I; 10:67180377-67180377 |
skin | malignant_melanoma | Substitution - coding silent |
c.2500C>G; p.R834G; 10:65920518-65920518 |
soft_tissue; striated_muscle | rhabdomyosarcoma | Substitution - Missense |
c.2447A>G; p.N816S; 10:65920571-65920571 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.2500C>G; p.R834G; 10:65920518-65920518 |
soft_tissue; striated_muscle | rhabdomyosarcoma; embryonal | Substitution - Missense |
c.2500C>G; p.R834G; 10:65920518-65920518 |
soft_tissue; striated_muscle | rhabdomyosarcoma; embryonal | Substitution - Missense |
c.1664T>C; p.M555T; 10:66379220-66379220 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2658G>T; p.M886I; 10:65920360-65920360 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - Missense |
c.2658G>T; p.M886I; 10:65920360-65920360 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1954C>T; p.Q652*; 10:66103180-66103180 |
skin | malignant_melanoma | Substitution - Nonsense |
c.165C>T; p.A55A; 10:67606984-67606984 |
bone; extraskeletal | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1894G>A; p.E632K; 10:66103240-66103240 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1536C>T; p.S512S; 10:66379348-66379348 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1999G>A; p.E667K; 10:66069468-66069468 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2654T>A; p.V885D; 10:65920364-65920364 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.2598A>G; p.E866E; 10:65920420-65920420 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2598A>G; p.E866E; 10:65920420-65920420 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1018C>T; p.Q340*; 10:67180346-67180346 |
skin | malignant_melanoma | Substitution - Nonsense |
c.640A>T; p.N214Y; 10:67219810-67219810 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1248G>A; p.A416A; 10:66766297-66766297 |
skin | malignant_melanoma | Substitution - coding silent |
c.1248G>A; p.A416A; 10:66766297-66766297 |
skin | malignant_melanoma | Substitution - coding silent |
c.1430delA; p.N477fs*21; 10:66520718-66520718 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2329C>T; p.H777Y; 10:65966683-65966683 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.849A>G; p.L283L; 10:67180515-67180515 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1060G>T; p.E354*; 10:66775512-66775512 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1060G>T; p.E354*; 10:66775512-66775512 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1956G>C; p.Q652H; 10:66103178-66103178 |
breast | carcinoma | Substitution - Missense |
c.553G>A; p.D185N; 10:67521868-67521868 |
skin | malignant_melanoma | Substitution - Missense |
c.2641C>T; p.H881Y; 10:65920377-65920377 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.980G>A; p.R327Q; 10:67180384-67180384 |
skin; scalp | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1243G>A; p.A415T; 10:66766302-66766302 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.980G>A; p.R327Q; 10:67180384-67180384 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.2400+1G>T; p.?; 10:65966611-65966611 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Unknown |
c.218G>A; p.G73E; 10:67606931-67606931 |
skin; shoulder | malignant_melanoma | Substitution - Missense |
c.841G>T; p.E281*; 10:67219609-67219609 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - Nonsense |
c.511C>T; p.Q171*; 10:67521910-67521910 |
skin | malignant_melanoma | Substitution - Nonsense |
c.2282G>T; p.C761F; 10:65966730-65966730 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2383G>A; p.E795K; 10:65966629-65966629 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.82delG; p.E28fs*4; 10:67647432-67647432 |
lung | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1107G>T; p.K369N; 10:66775465-66775465 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.477G>T; p.E159D; 10:67521944-67521944 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1247C>T; p.A416V; 10:66766298-66766298 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1247C>T; p.A416V; 10:66766298-66766298 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.1247C>T; p.A416V; 10:66766298-66766298 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1375A>G; p.I459V; 10:66520773-66520773 |
liver | carcinoma | Substitution - Missense |
c.1133G>A; p.R378H; 10:66766412-66766412 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.1375A>G; p.I459V; 10:66520773-66520773 |
liver | carcinoma | Substitution - Missense |
c.141G>A; p.R47R; 10:67607008-67607008 |
skin | malignant_melanoma | Substitution - coding silent |
c.1771G>A; p.E591K; 10:66280583-66280583 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.141G>A; p.R47R; 10:67607008-67607008 |
skin | malignant_melanoma | Substitution - coding silent |
c.1281G>T; p.E427D; 10:66766264-66766264 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1281G>T; p.E427D; 10:66766264-66766264 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.84G>A; p.E28E; 10:67647430-67647430 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.141G>A; p.R47R; 10:67607008-67607008 |
skin | malignant_melanoma | Substitution - coding silent |
c.1281G>T; p.E427D; 10:66766264-66766264 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.1281G>T; p.E427D; 10:66766264-66766264 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.67G>T; p.V23L; 10:67647447-67647447 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1301C>T; p.S434F; 10:66621765-66621765 |
skin | malignant_melanoma | Substitution - Missense |
c.2567_2568insA; p.P857fs*4; 10:65920450-65920451 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.2567_2568insA; p.P857fs*4; 10:65920450-65920451 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.567C>T; p.F189F; 10:67521854-67521854 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.567C>T; p.F189F; 10:67521854-67521854 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.1891G>C; p.E631Q; 10:66103243-66103243 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.331G>A; p.D111N; 10:67539631-67539631 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1047+1G>A; p.?; 10:67180316-67180316 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.2464G>T; p.V822L; 10:65920554-65920554 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1236delA; p.E413fs*14; 10:66766309-66766309 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Deletion - Frameshift |
c.822A>T; p.G274G; 10:67219628-67219628 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.2449G>A; p.A817T; 10:65920569-65920569 |
liver | carcinoma | Substitution - Missense |
c.1369C>T; p.P457S; 10:66621697-66621697 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2563A>G; p.K855E; 10:65920455-65920455 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.1195C>T; p.L399F; 10:66766350-66766350 |
skin | malignant_melanoma | Substitution - Missense |
c.2449G>A; p.A817T; 10:65920569-65920569 |
liver | carcinoma | Substitution - Missense |
c.2563A>G; p.K855E; 10:65920455-65920455 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.2563A>G; p.K855E; 10:65920455-65920455 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.847T>C; p.L283L; 10:67180517-67180517 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.847T>C; p.L283L; 10:67180517-67180517 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1339A>G; p.I447V; 10:66621727-66621727 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1406G>C; p.R469T; 10:66520742-66520742 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.891A>G; p.R297R; 10:67180473-67180473 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2613C>T; p.V871V; 10:65920405-65920405 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1406G>C; p.R469T; 10:66520742-66520742 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1465C>T; p.H489Y; 10:66520683-66520683 |
skin | malignant_melanoma | Substitution - Missense |
c.747C>T; p.L249L; 10:67219703-67219703 |
skin | malignant_melanoma | Substitution - coding silent |
c.279A>C; p.E93D; 10:67606870-67606870 |
skin | malignant_melanoma | Substitution - Missense |
c.546A>C; p.E182D; 10:67521875-67521875 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1433C>A; p.T478N; 10:66520715-66520715 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.946G>A; p.D316N; 10:67180418-67180418 |
skin | malignant_melanoma | Substitution - Missense |
c.580-1G>A; p.?; 10:67219871-67219871 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Unknown |
c.2016G>T; p.K672N; 10:66069451-66069451 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.277G>A; p.E93K; 10:67606872-67606872 |
skin; neck | malignant_melanoma | Substitution - Missense |
c.1309A>G; p.T437A; 10:66621757-66621757 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1881T>A; p.I627I; 10:66280473-66280473 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1627C>T; p.R543W; 10:66379257-66379257 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.148G>A; p.G50R; 10:67607001-67607001 |
skin | malignant_melanoma | Substitution - Missense |
c.1302C>T; p.S434S; 10:66621764-66621764 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1220G>T; p.R407L; 10:66766325-66766325 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1190T>G; p.L397W; 10:66766355-66766355 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2520G>T; p.G840G; 10:65920498-65920498 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1977G>T; p.R659S; 10:66103157-66103157 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2376_2377insA; p.G793fs*68; 10:65966635-65966636 |
breast | carcinoma | Insertion - Frameshift |
c.2398G>T; p.A800S; 10:65966614-65966614 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2470A>T; p.M824L; 10:65920548-65920548 |
liver | carcinoma | Substitution - Missense |
c.819G>T; p.L273L; 10:67219631-67219631 |
skin; upper_leg | malignant_melanoma | Substitution - coding silent |
c.753A>C; p.V251V; 10:67219697-67219697 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1935C>T; p.V645V; 10:66103199-66103199 |
skin | malignant_melanoma | Substitution - coding silent |
c.1145T>C; p.I382T; 10:66766400-66766400 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.412C>T; p.L138F; 10:67539550-67539550 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.956G>A; p.C319Y; 10:67180408-67180408 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - Missense |
c.675T>C; p.C225C; 10:67219775-67219775 |
skin | malignant_melanoma | Substitution - coding silent |
c.1488C>T; p.A496A; 10:66520660-66520660 |
skin | malignant_melanoma | Substitution - coding silent |
c.1645C>T; p.H549Y; 10:66379239-66379239 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1488C>T; p.A496A; 10:66520660-66520660 |
breast | carcinoma | Substitution - coding silent |
c.1758G>T; p.V586V; 10:66280596-66280596 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1187T>G; p.L396R; 10:66766358-66766358 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.721G>A; p.V241I; 10:67219729-67219729 |
skin | malignant_melanoma | Substitution - Missense |
c.1386T>C; p.A462A; 10:66520762-66520762 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.721G>A; p.V241I; 10:67219729-67219729 |
skin | malignant_melanoma | Substitution - Missense |
c.1483G>A; p.E495K; 10:66520665-66520665 |
skin | malignant_melanoma | Substitution - Missense |
c.1002C>T; p.A334A; 10:67180362-67180362 |
skin | malignant_melanoma | Substitution - coding silent |
c.1656G>T; p.T552T; 10:66379228-66379228 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1914C>T; p.D638D; 10:66103220-66103220 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2569C>T; p.P857S; 10:65920449-65920449 |
skin | malignant_melanoma | Substitution - Missense |
c.1750A>G; p.T584A; 10:66280604-66280604 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1107G>A; p.K369K; 10:66775465-66775465 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2205G>T; p.A735A; 10:65988752-65988752 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2568delA; p.K856fs*3; 10:65920450-65920450 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1794G>A; p.L598L; 10:66280560-66280560 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.2568delA; p.K856fs*3; 10:65920450-65920450 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2568delA; p.K856fs*3; 10:65920450-65920450 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2568delA; p.K856fs*3; 10:65920450-65920450 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2568_2569insA; p.P857fs*4; 10:65920449-65920450 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.2568_2569insA; p.P857fs*4; 10:65920449-65920450 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.521A>G; p.Y174C; 10:67521900-67521900 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2568_2569insA; p.P857fs*4; 10:65920449-65920450 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.2568_2569insA; p.P857fs*4; 10:65920449-65920450 |
liver | carcinoma; hepatocellular_carcinoma | Insertion - Frameshift |
c.2568_2569insA; p.P857fs*4; 10:65920449-65920450 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1144A>T; p.I382L; 10:66766401-66766401 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1471C>T; p.H491Y; 10:66520677-66520677 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1060_1061insA; p.R355fs*3; 10:66775511-66775512 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - Frameshift |
c.2672G>A; p.G891E; 10:65920346-65920346 |
skin | malignant_melanoma | Substitution - Missense |
c.1228G>A; p.E410K; 10:66766317-66766317 |
skin | malignant_melanoma | Substitution - Missense |
c.326C>A; p.T109K; 10:67539636-67539636 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1006C>T; p.R336C; 10:67180358-67180358 |
skin | malignant_melanoma | Substitution - Missense |
c.1006C>T; p.R336C; 10:67180358-67180358 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1006C>T; p.R336C; 10:67180358-67180358 |
breast | carcinoma | Substitution - Missense |
c.843G>A; p.E281E; 10:67219607-67219607 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1006C>T; p.R336C; 10:67180358-67180358 |
skin | malignant_melanoma | Substitution - Missense |
c.1006C>T; p.R336C; 10:67180358-67180358 |
skin | malignant_melanoma | Substitution - Missense |
c.327A>G; p.T109T; 10:67539635-67539635 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.715G>A; p.D239N; 10:67219735-67219735 |
skin | malignant_melanoma | Substitution - Missense |
c.503C>T; p.S168F; 10:67521918-67521918 |
skin | malignant_melanoma | Substitution - Missense |
c.1519C>A; p.L507I; 10:66520629-66520629 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1674C>T; p.Y558Y; 10:66379210-66379210 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1112G>A; p.R371K; 10:66775460-66775460 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1674C>T; p.Y558Y; 10:66379210-66379210 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.945G>A; p.A315A; 10:67180419-67180419 |
bone; extraskeletal | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1606G>T; p.A536S; 10:66379278-66379278 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.793C>A; p.P265T; 10:67219657-67219657 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.789A>T; p.T263T; 10:67219661-67219661 |
ovary | other; neoplasm | Substitution - coding silent |
c.2374C>A; p.L792M; 10:65966638-65966638 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2374C>A; p.L792M; 10:65966638-65966638 |
breast | carcinoma | Substitution - Missense |
c.228T>A; p.I76I; 10:67606921-67606921 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.217G>A; p.G73R; 10:67606932-67606932 |
skin | malignant_melanoma | Substitution - Missense |
c.1865G>A; p.C622Y; 10:66280489-66280489 |
central_nervous_system; brain | glioma; astrocytoma_Grade_II | Substitution - Missense |
c.2653G>T; p.V885F; 10:65920365-65920365 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1846A>C; p.T616P; 10:66280508-66280508 |
pancreas | NS | Substitution - Missense |
c.841G>A; p.E281K; 10:67219609-67219609 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2067T>G; p.A689A; 10:66069400-66069400 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.841G>A; p.E281K; 10:67219609-67219609 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.293G>T; p.S98I; 10:67539669-67539669 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1603C>T; p.R535C; 10:66379281-66379281 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.607G>A; p.E203K; 10:67219843-67219843 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2160-1G>T; p.?; 10:65988798-65988798 |
lung | carcinoma; squamous_cell_carcinoma | Unknown |