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

Basic Information

Gene ID

50515

Name

CHST11

Synonymous

carbohydrate (chondroitin 4) sulfotransferase 11;CHST11;carbohydrate (chondroitin 4) sulfotransferase 11

Definition

C4S-1|IgH/CHST11 fusion|carbohydrate sulfotransferase 11|chondroitin 4-O-sulfotransferase 1

Position

12q

Gene Type

protein-coding

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.656G>A; p.R219H; 12:104757400-104757400

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.704T>A; p.V235D; 12:104757448-104757448

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.369G>T; p.V123V; 12:104757113-104757113

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.469G>T; p.V157F; 12:104757213-104757213

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.814C>T; p.H272Y; 12:104757558-104757558

skinmalignant_melanomaSubstitution - Missense

c.993C>T; p.Y331Y; 12:104757737-104757737

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.5A>C; p.K2T; 12:104457416-104457416

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.503G>A; p.S168N; 12:104757247-104757247

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.451C>T; p.P151S; 12:104757195-104757195

skin; scalpcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.336G>A; p.V112V; 12:104757080-104757080

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.402C>T; p.L134L; 12:104757146-104757146

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.661C>T; p.R221W; 12:104757405-104757405

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.547C>T; p.L183L; 12:104757291-104757291

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.661C>T; p.R221W; 12:104757405-104757405

large_intestine; colonadenomaSubstitution - Missense

c.179T>A; p.L60Q; 12:104601966-104601966

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.852G>T; p.E284D; 12:104757596-104757596

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.473C>A; p.S158Y; 12:104757217-104757217

prostatecarcinomaSubstitution - Missense

c.84G>A; p.L28L; 12:104457495-104457495

stomachcarcinoma; diffuse_adenocarcinomaSubstitution - coding silent

c.524G>A; p.R175H; 12:104757268-104757268

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.865G>A; p.V289I; 12:104757609-104757609

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.348C>T; p.H116H; 12:104757092-104757092

prostatecarcinomaSubstitution - coding silent

c.125G>T; p.R42L; 12:104601912-104601912

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphomaSubstitution - Missense

c.348C>T; p.H116H; 12:104757092-104757092

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.840G>C; p.E280D; 12:104757584-104757584

central_nervous_system; braingliomaSubstitution - Missense

c.559G>A; p.E187K; 12:104757303-104757303

skinmalignant_melanomaSubstitution - Missense

c.600C>T; p.F200F; 12:104757344-104757344

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.759G>T; p.E253D; 12:104757503-104757503

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1000T>C; p.Y334H; 12:104757744-104757744

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.475G>A; p.A159T; 12:104757219-104757219

breastcarcinomaSubstitution - Missense

c.475G>A; p.A159T; 12:104757219-104757219

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.475G>A; p.A159T; 12:104757219-104757219

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.475G>A; p.A159T; 12:104757219-104757219

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.475G>A; p.A159T; 12:104757219-104757219

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.475G>A; p.A159T; 12:104757219-104757219

pancreascarcinomaSubstitution - Missense

c.1008C>T; p.L336L; 12:104757752-104757752

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.284C>A; p.T95K; 12:104757028-104757028

thyroidother; neoplasmSubstitution - Missense

c.905C>T; p.P302L; 12:104757649-104757649

skinmalignant_melanomaSubstitution - Missense

c.81C>A; p.I27I; 12:104457492-104457492

thyroidcarcinomaSubstitution - coding silent

c.553G>C; p.V185L; 12:104757297-104757297

pancreascarcinomaSubstitution - Missense

c.469G>A; p.V157I; 12:104757213-104757213

stomachadenocarcinomaSubstitution - Missense

c.170G>A; p.R57Q; 12:104601957-104601957

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.170G>A; p.R57Q; 12:104601957-104601957

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.781A>C; p.T261P; 12:104757525-104757525

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.525C>A; p.R175R; 12:104757269-104757269

oesophaguscarcinoma; adenocarcinomaSubstitution - coding silent

c.525C>A; p.R175R; 12:104757269-104757269

oesophaguscarcinoma; adenocarcinomaSubstitution - coding silent

c.857C>T; p.S286F; 12:104757601-104757601

pancreascarcinomaSubstitution - Missense

c.398G>A; p.R133Q; 12:104757142-104757142

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.398G>A; p.R133Q; 12:104757142-104757142

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.700G>A; p.D234N; 12:104757444-104757444

skinmalignant_melanomaSubstitution - Missense

c.521A>G; p.H174R; 12:104757265-104757265

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.769G>A; p.E257K; 12:104757513-104757513

pancreascarcinomaSubstitution - Missense

c.315C>G; p.N105K; 12:104757059-104757059

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.715G>T; p.E239*; 12:104757459-104757459

livercarcinomaSubstitution - Nonsense

c.93C>G; p.F31L; 12:104457504-104457504

skinmalignant_melanomaSubstitution - Missense

c.590G>A; p.R197H; 12:104757334-104757334

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.474C>T; p.S158S; 12:104757218-104757218

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.937G>A; p.E313K; 12:104757681-104757681

urinary_tract; bladdercarcinomaSubstitution - Missense

c.825C>T; p.L275L; 12:104757569-104757569

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.897G>A; p.L299L; 12:104757641-104757641

urinary_tract; bladdercarcinomaSubstitution - coding silent

c.455C>T; p.A152V; 12:104757199-104757199

skinmalignant_melanomaSubstitution - Missense

c.751C>T; p.R251W; 12:104757495-104757495

breastcarcinomaSubstitution - Missense

c.714G>T; p.E238D; 12:104757458-104757458

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.211C>T; p.L71F; 12:104756955-104756955

haematopoietic_and_lymphoid_tissue; central_nervous_systemlymphoid_neoplasm; primary_central_nervous_system_lymphomaSubstitution - Missense

c.798C>T; p.C266C; 12:104757542-104757542

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.411C>T; p.V137V; 12:104757155-104757155

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.800A>C; p.H267P; 12:104757544-104757544

urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.705C>G; p.V235V; 12:104757449-104757449

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.669C>T; p.N223N; 12:104757413-104757413

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.191A>G; p.Y64C; 12:104601978-104601978

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.175C>T; p.P59S; 12:104601962-104601962

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.417C>T; p.T139T; 12:104757161-104757161

breastcarcinomaSubstitution - coding silent

c.985C>T; p.Q329*; 12:104757729-104757729

oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Nonsense

c.837C>G; p.Y279*; 12:104757581-104757581

skinmalignant_melanomaSubstitution - Nonsense

c.662G>A; p.R221Q; 12:104757406-104757406

autonomic_ganglianeuroblastomaSubstitution - Missense

c.662G>A; p.R221Q; 12:104757406-104757406

livercarcinomaSubstitution - Missense

c.83T>G; p.L28R; 12:104457494-104457494

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.125G>A; p.R42Q; 12:104601912-104601912

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.1026T>G; p.N342K; 12:104757770-104757770

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.125G>A; p.R42Q; 12:104601912-104601912

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.801T>C; p.H267H; 12:104757545-104757545

thyroidother; neoplasmSubstitution - coding silent

c.992A>G; p.Y331C; 12:104757736-104757736

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.864C>T; p.Y288Y; 12:104757608-104757608

breastcarcinomaSubstitution - coding silent

c.864C>T; p.Y288Y; 12:104757608-104757608

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.349G>A; p.E117K; 12:104757093-104757093

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.296G>A; p.R99Q; 12:104757040-104757040

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.645G>T; p.K215N; 12:104757389-104757389

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.468C>T; p.H156H; 12:104757212-104757212

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.711C>T; p.F237F; 12:104757455-104757455

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.994G>A; p.E332K; 12:104757738-104757738

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.711C>T; p.F237F; 12:104757455-104757455

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.994G>A; p.E332K; 12:104757738-104757738

skinmalignant_melanomaSubstitution - Missense

c.568G>A; p.E190K; 12:104757312-104757312

skinmalignant_melanomaSubstitution - Missense

c.468C>T; p.H156H; 12:104757212-104757212

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.711C>T; p.F237F; 12:104757455-104757455

ovarycarcinoma; serous_carcinomaSubstitution - coding silent

c.994G>A; p.E332K; 12:104757738-104757738

oesophaguscarcinomaSubstitution - Missense

c.711C>T; p.F237F; 12:104757455-104757455

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.480C>T; p.N160N; 12:104757224-104757224

skinmalignant_melanomaSubstitution - coding silent

c.1028A>G; p.Y343C; 12:104757772-104757772

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.269G>A; p.R90Q; 12:104757013-104757013

skinmalignant_melanomaSubstitution - Missense

c.269G>A; p.R90Q; 12:104757013-104757013

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.913G>A; p.A305T; 12:104757657-104757657

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.397C>T; p.R133W; 12:104757141-104757141

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.567C>T; p.F189F; 12:104757311-104757311

bone; ribchondrosarcomaSubstitution - coding silent

c.567C>T; p.F189F; 12:104757311-104757311

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.241C>T; p.R81W; 12:104756985-104756985

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense