Cancer metastasis gene database Home
Cancer metastasis database
General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

51466

Name

EVL

Synonymous

Enah/Vasp-like;EVL;Enah/Vasp-like

Definition

ena/VASP-like protein|ena/vasodilator-stimulated phosphoprotein-like

Position

14q32.2

Gene Type

protein-coding

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.558_559insC; p.P190fs*108; 14:100128589-100128590

 large_intestine; caecumcarcinoma; adenocarcinomaInsertion - Frameshift

c.558_559insC; p.P190fs*108; 14:100128589-100128590

 large_intestine; coloncarcinoma; adenocarcinomaInsertion - Frameshift

c.558_559insC; p.P190fs*108; 14:100128589-100128590

 large_intestine; caecumcarcinoma; adenocarcinomaInsertion - Frameshift

c.933C>T; p.T311T; 14:100135937-100135937

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.115A>G; p.N39D; 14:100084790-100084790

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.303C>A; p.T101T; 14:100097603-100097603

 lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.889G>A; p.E297K; 14:100132768-100132768

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.889G>A; p.E297K; 14:100132768-100132768

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.451C>T; p.R151C; 14:100126735-100126735

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.350_352delAAG; p.E118delE; 14:100097650-100097652

 ovarycarcinoma; serous_carcinomaDeletion - In frame

c.988C>T; p.R330W; 14:100137601-100137601

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_leukaemiaSubstitution - Missense

c.988C>T; p.R330W; 14:100137601-100137601

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.154G>A; p.V52I; 14:100084829-100084829

 central_nervous_system; braingliomaSubstitution - Missense

c.974G>A; p.R325Q; 14:100137587-100137587

 large_intestine; coloncarcinomaSubstitution - Missense

c.974G>A; p.R325Q; 14:100137587-100137587

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.528C>A; p.S176R; 14:100128559-100128559

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.199A>G; p.I67V; 14:100097499-100097499

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_leukaemiaSubstitution - Missense

c.535G>A; p.V179I; 14:100128566-100128566

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; mantle_cell_lymphomaSubstitution - Missense

c.1252A>G; p.T418A; 14:100143733-100143733

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.559delC; p.P189fs*41; 14:100128590-100128590

 large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.231G>T; p.T77T; 14:100097531-100097531

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.776G>A; p.R259Q; 14:100129621-100129621

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.342G>A; p.M114I; 14:100097642-100097642

 oesophagus; middle_thirdcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.569C>T; p.P190L; 14:100128600-100128600

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.569C>T; p.P190L; 14:100128600-100128600

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1009C>A; p.P337T; 14:100137622-100137622

 skinmalignant_melanomaSubstitution - Missense

c.709G>T; p.V237F; 14:100128740-100128740

 bone; iliumEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

c.680C>T; p.A227V; 14:100128711-100128711

 large_intestine; coloncarcinomaSubstitution - Missense

c.680C>T; p.A227V; 14:100128711-100128711

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1075C>G; p.Q359E; 14:100137783-100137783

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.568C>A; p.P190T; 14:100128599-100128599

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.568C>A; p.P190T; 14:100128599-100128599

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.568C>A; p.P190T; 14:100128599-100128599

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.365C>T; p.S122F; 14:100123545-100123545

 skinmalignant_melanomaSubstitution - Missense

c.1164G>T; p.E388D; 14:100141738-100141738

 stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.374G>A; p.R125H; 14:100123554-100123554

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.329C>T; p.A110V; 14:100097629-100097629

 skinmalignant_melanomaSubstitution - Missense

c.1102C>T; p.P368S; 14:100141187-100141187

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1047delA; p.K350fs*17; 14:100137755-100137755

 endometriumcarcinoma; endometrioid_carcinomaDeletion - Frameshift

c.880_882delAAG; p.K294delK; 14:100132759-100132761

 large_intestine; coloncarcinomaDeletion - In frame

c.473G>A; p.R158K; 14:100126757-100126757

 oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Missense

c.1203G>A; p.K401K; 14:100141777-100141777

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.926C>T; p.P309L; 14:100135930-100135930

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.926C>T; p.P309L; 14:100135930-100135930

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.570C>T; p.P190P; 14:100128601-100128601

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1031+2T>C; p.?; 14:100137646-100137646

 stomachcarcinoma; adenocarcinomaUnknown

c.1009C>G; p.P337A; 14:100137622-100137622

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.109C>T; p.R37W; 14:100084784-100084784

 stomachadenocarcinomaSubstitution - Missense

c.738C>T; p.G246G; 14:100129583-100129583

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1090T>C; p.S364P; 14:100137798-100137798

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1176G>T; p.E392D; 14:100141750-100141750

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.567A>C; p.P189P; 14:100128598-100128598

 ovarycarcinoma; serous_carcinomaSubstitution - coding silent

c.567A>C; p.P189P; 14:100128598-100128598

 ovarycarcinoma; serous_carcinomaSubstitution - coding silent

c.1084C>G; p.P362A; 14:100137792-100137792

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.364T>C; p.S122P; 14:100123544-100123544

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.495C>T; p.I165I; 14:100128526-100128526

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.992G>A; p.S331N; 14:100137605-100137605

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.201C>T; p.I67I; 14:100097501-100097501

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.1141G>A; p.D381N; 14:100141226-100141226

 skinmalignant_melanomaSubstitution - Missense

c.569_570CC>TT; p.P190L; 14:100128600-100128601

 skinmalignant_melanomaSubstitution - Missense

c.998C>T; p.S333L; 14:100137611-100137611

 oesophaguscarcinomaSubstitution - Missense

c.225G>A; p.Q75Q; 14:100097525-100097525

 livercarcinomaSubstitution - coding silent

c.716G>A; p.R239Q; 14:100128747-100128747

 skinmalignant_melanomaSubstitution - Missense

c.746C>T; p.P249L; 14:100129591-100129591

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1118A>G; p.N373S; 14:100141203-100141203

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.991A>T; p.S331C; 14:100137604-100137604

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.452G>A; p.R151H; 14:100126736-100126736

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.452G>A; p.R151H; 14:100126736-100126736

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.590C>T; p.T197I; 14:100128621-100128621

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.590C>T; p.T197I; 14:100128621-100128621

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.590C>T; p.T197I; 14:100128621-100128621

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.153C>T; p.V51V; 14:100084828-100084828

 skinmalignant_melanomaSubstitution - coding silent

c.875_877delAGA; p.K294delK; 14:100132754-100132756

 large_intestinecarcinoma; adenocarcinomaDeletion - In frame

c.1105G>A; p.A369T; 14:100141190-100141190

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.195T>C; p.Y65Y; 14:100097495-100097495

 lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.251G>T; p.R84L; 14:100097551-100097551

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1079C>T; p.S360L; 14:100137787-100137787

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1032-4G>A; p.?; 14:100137736-100137736

 pancreascarcinomaUnknown

c.58G>A; p.D20N; 14:100084733-100084733

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_leukaemiaSubstitution - Missense

c.136A>G; p.S46G; 14:100084811-100084811

 eye; uveal_tractmalignant_melanoma; spindleSubstitution - Missense

c.726C>T; p.D242D; 14:100129571-100129571

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1037C>T; p.P346L; 14:100137745-100137745

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1037C>T; p.P346L; 14:100137745-100137745

 stomachcarcinoma; adenocarcinomaSubstitution - Missense