Epithelial-Mesenchymal Transition gene database (dbEMT) Home
dbEMT
dbEMT 2.0
General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

50616

Name

IL22

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.229G>A; p.E77K; 12:68252787-68252787

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.101C>T; p.A34V; 12:68253348-68253348

 skinmalignant_melanomaSubstitution - Missense

c.235C>G; p.L79V; 12:68252781-68252781

 livercarcinomaSubstitution - Missense

c.178G>A; p.A60T; 12:68253271-68253271

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.75C>T; p.A25A; 12:68253374-68253374

 skinmalignant_melanomaSubstitution - coding silent

c.156C>T; p.I52I; 12:68253293-68253293

 lungcarcinoma; small_cell_carcinomaSubstitution - coding silent

c.412G>A; p.D138N; 12:68251563-68251563

 skinmalignant_melanomaSubstitution - Missense

c.238_239TT>CC; p.F80>?; 12:68252777-68252778

 lungcarcinoma; adenocarcinomaComplex

c.244G>T; p.G82*; 12:68252772-68252772

 pancreascarcinomaSubstitution - Nonsense

c.356T>C; p.V119A; 12:68252544-68252544

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.227G>A; p.G76E; 12:68252789-68252789

 skin; anklemalignant_melanoma; acral_lentiginousSubstitution - Missense

c.293T>A; p.F98Y; 12:68252607-68252607

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.462+7C>A; p.?; 12:68251506-68251506

 pancreascarcinomaUnknown

c.55A>G; p.S19G; 12:68253394-68253394

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.463C>A; p.L155I; 12:68248876-68248876

 adrenal_gland; adrenal_glandadrenal_cortical_carcinoma; functioningSubstitution - Missense

c.273G>T; p.L91L; 12:68252627-68252627

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.375C>A; p.L125L; 12:68252525-68252525

 kidneyother; neoplasmSubstitution - coding silent

c.192C>T; p.S64S; 12:68252824-68252824

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.163C>T; p.R55C; 12:68253286-68253286

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.8C>A; p.A3D; 12:68253441-68253441

 breastcarcinomaSubstitution - Missense

c.113C>T; p.S38F; 12:68253336-68253336

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.113C>T; p.S38F; 12:68253336-68253336

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.217C>T; p.R73C; 12:68252799-68252799

 skinmalignant_melanomaSubstitution - Missense

c.217C>T; p.R73C; 12:68252799-68252799

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.496G>T; p.E166*; 12:68248843-68248843

 endometriumcarcinoma; serous_carcinomaSubstitution - Nonsense

c.397-1G>C; p.?; 12:68251579-68251579

 skinmalignant_melanomaUnknown

c.403G>C; p.E135Q; 12:68251572-68251572

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.168C>T; p.T56T; 12:68253281-68253281

 livercarcinomaSubstitution - coding silent

c.330G>T; p.R110S; 12:68252570-68252570

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.18A>G; p.K6K; 12:68253431-68253431

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.218G>A; p.R73H; 12:68252798-68252798

 stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.218G>A; p.R73H; 12:68252798-68252798

 stomachadenocarcinomaSubstitution - Missense

c.244G>A; p.G82R; 12:68252772-68252772

 thyroidcarcinomaSubstitution - Missense

c.244G>A; p.G82R; 12:68252772-68252772

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.244G>A; p.G82R; 12:68252772-68252772

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.63C>T; p.L21L; 12:68253386-68253386

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.480G>C; p.E160D; 12:68248859-68248859

 breastcarcinoma; HER-positive_carcinomaSubstitution - Missense

c.170T>C; p.F57S; 12:68253279-68253279

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.428G>T; p.R143M; 12:68251547-68251547

 oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.487G>T; p.A163S; 12:68248852-68248852

 central_nervous_system; braingliomaSubstitution - Missense

c.487G>T; p.A163S; 12:68248852-68248852

 lungcarcinoma; large_cell_carcinomaSubstitution - Missense

c.284T>C; p.V95A; 12:68252616-68252616

 stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.253-1G>A; p.?; 12:68252648-68252648

 lungcarcinoma; small_cell_carcinomaUnknown

c.45C>A; p.T15T; 12:68253404-68253404

 lungcarcinoma; small_cell_carcinomaSubstitution - coding silent

c.520C>G; p.L174V; 12:68248819-68248819

 breastcarcinomaSubstitution - Missense

c.248T>C; p.V83A; 12:68252768-68252768

 boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

c.183G>C; p.K61N; 12:68253266-68253266

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.183G>C; p.K61N; 12:68253266-68253266

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

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