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

Basic Information

Gene ID

4782

Name

NFIC

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.1151C>T; p.A384V; 19:3452575-3452575

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.108C>T; p.H36H; 19:3381816-3381816

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.1475A>C; p.Q492P; 19:3456628-3456628

 stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.76C>T; p.Q26*; 19:3381784-3381784

 breastcarcinomaSubstitution - Nonsense

c.629G>C; p.S210T; 19:3433539-3433539

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1350A>C; p.K450N; 19:3453870-3453870

 thyroidother; neoplasmSubstitution - Missense

c.108C>G; p.H36Q; 19:3381816-3381816

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.191C>T; p.A64V; 19:3381899-3381899

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.939G>A; p.S313S; 19:3449021-3449021

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - coding silent

c.225C>G; p.I75M; 19:3381933-3381933

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.716C>T; p.S239F; 19:3434310-3434310

 skin; mucosalmalignant_melanomaSubstitution - Missense

c.1335delC; p.P447fs*36; 19:3453855-3453855

 stomachcarcinoma; intestinal_adenocarcinomaDeletion - Frameshift

c.712T>G; p.F238V; 19:3434306-3434306

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.189G>A; p.W63*; 19:3381897-3381897

 skinmalignant_melanomaSubstitution - Nonsense

c.748G>A; p.D250N; 19:3434342-3434342

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1051C>T; p.H351Y; 19:3449133-3449133

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.410C>T; p.T137I; 19:3382118-3382118

 skinmalignant_melanomaSubstitution - Missense

c.323G>A; p.R108H; 19:3382031-3382031

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.323G>A; p.R108H; 19:3382031-3382031

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.399G>A; p.P133P; 19:3382107-3382107

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.399G>A; p.P133P; 19:3382107-3382107

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.629G>T; p.S210I; 19:3433539-3433539

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.824C>T; p.S275L; 19:3435100-3435100

 pancreascarcinomaSubstitution - Missense

c.279G>T; p.P93P; 19:3381987-3381987

 livercarcinomaSubstitution - coding silent

c.1086C>T; p.S362S; 19:3452510-3452510

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.291C>G; p.L97L; 19:3381999-3381999

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.1124C>T; p.T375M; 19:3452548-3452548

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1070G>A; p.S357N; 19:3452494-3452494

 prostatecarcinomaSubstitution - Missense

c.502G>A; p.D168N; 19:3382210-3382210

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1411G>A; p.D471N; 19:3456564-3456564

 breastcarcinomaSubstitution - Missense

c.322C>A; p.R108S; 19:3382030-3382030

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.1430G>A; p.R477H; 19:3456583-3456583

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.892A>T; p.T298S; 19:3435168-3435168

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.141G>A; p.A47A; 19:3381849-3381849

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.17C>A; p.P6Q; 19:3381725-3381725

 boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

c.992C>T; p.P331L; 19:3449074-3449074

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1006C>T; p.R336C; 19:3449088-3449088

 skinmalignant_melanomaSubstitution - Missense

c.688G>A; p.V230M; 19:3434282-3434282

 pancreascarcinomaSubstitution - Missense

c.743C>T; p.A248V; 19:3434337-3434337

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.526C>T; p.R176C; 19:3382234-3382234

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.945G>A; p.P315P; 19:3449027-3449027

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.1152C>T; p.A384A; 19:3452576-3452576

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.717C>T; p.S239S; 19:3434311-3434311

 skinmalignant_melanomaSubstitution - coding silent

c.196C>T; p.R66W; 19:3381904-3381904

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.896G>A; p.S299N; 19:3435172-3435172

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.1241C>T; p.P414L; 19:3452665-3452665

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.360G>A; p.R120R; 19:3382068-3382068

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1068G>A; p.R356R; 19:3452492-3452492

 skinmalignant_melanomaSubstitution - coding silent

c.679C>T; p.R227W; 19:3433589-3433589

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1188G>T; p.P396P; 19:3452612-3452612

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.359G>A; p.R120Q; 19:3382067-3382067

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1206G>A; p.S402S; 19:3452630-3452630

 soft_tissue; striated_musclerhabdomyosarcoma; embryonalSubstitution - coding silent

c.1206G>A; p.S402S; 19:3452630-3452630

 soft_tissue; striated_musclerhabdomyosarcomaSubstitution - coding silent

c.136C>T; p.R46C; 19:3381844-3381844

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.260T>G; p.I87S; 19:3381968-3381968

 skinmalignant_melanomaSubstitution - Missense

c.645C>T; p.G215G; 19:3433555-3433555

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1105A>G; p.T369A; 19:3452529-3452529

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.25G>C; p.E9Q; 19:3381733-3381733

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1103C>T; p.T368M; 19:3452527-3452527

 pancreascarcinomaSubstitution - Missense

c.140C>T; p.A47V; 19:3381848-3381848

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_leukaemiaSubstitution - Missense

c.82C>T; p.R28W; 19:3381790-3381790

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.358C>T; p.R120W; 19:3382066-3382066

 oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Missense

c.1157G>A; p.R386H; 19:3452581-3452581

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.185A>G; p.K62R; 19:3381893-3381893

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.204G>T; p.L68L; 19:3381912-3381912

 lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.959A>T; p.E320V; 19:3449041-3449041

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.932-1G>A; p.?; 19:3449013-3449013

 skinmalignant_melanomaUnknown

c.1168C>T; p.H390Y; 19:3452592-3452592

 thyroidcarcinomaSubstitution - Missense

c.469C>T; p.P157S; 19:3382177-3382177

 NSmalignant_melanomaSubstitution - Missense

c.988T>C; p.S330P; 19:3449070-3449070

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.988T>C; p.S330P; 19:3449070-3449070

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.988T>C; p.S330P; 19:3449070-3449070

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.988T>C; p.S330P; 19:3449070-3449070

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.988T>C; p.S330P; 19:3449070-3449070

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.988T>C; p.S330P; 19:3449070-3449070

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.988T>C; p.S330P; 19:3449070-3449070

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.988T>C; p.S330P; 19:3449070-3449070

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.988T>C; p.S330P; 19:3449070-3449070

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.988T>C; p.S330P; 19:3449070-3449070

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.988T>C; p.S330P; 19:3449070-3449070

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.718C>T; p.L240L; 19:3434312-3434312

 skinmalignant_melanomaSubstitution - coding silent

c.170C>T; p.P57L; 19:3381878-3381878

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.170C>T; p.P57L; 19:3381878-3381878

 skinmalignant_melanomaSubstitution - Missense

c.923T>C; p.M308T; 19:3435199-3435199

 upper_aerodigestive_tract; mouthcarcinomaSubstitution - Missense

c.923T>C; p.M308T; 19:3435199-3435199

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.422G>A; p.R141H; 19:3382130-3382130

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.590G>A; p.S197N; 19:3425160-3425160

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.27G>T; p.E9D; 19:3381735-3381735

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.319C>T; p.R107W; 19:3382027-3382027

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

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