Cell senescence gene database Home
Cell senescence database
General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

3665

Name

IRF7

Synonymous

interferon regulatory factor 7;IRF7;interferon regulatory factor 7

Definition

IRF-7|interferon regulatory factor-7H

Position

11p15.5

Gene Type

protein-coding

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.825_826insAG; p.H278fs*28; 11:613845-613846

 skin; abdomenmalignant_melanomaInsertion - Frameshift

c.1182C>T; p.G394G; 11:613300-613300

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1492G>A; p.A498T; 11:612704-612704

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.366G>A; p.R122R; 11:614864-614864

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.366G>A; p.R122R; 11:614864-614864

 thyroidother; neoplasmSubstitution - coding silent

c.640T>C; p.W214R; 11:614252-614252

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.778G>A; p.G260R; 11:613978-613978

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; mantle_cell_lymphomaSubstitution - Missense

c.94C>T; p.L32F; 11:615225-615225

 skinmalignant_melanomaSubstitution - Missense

c.1412G>T; p.C471F; 11:612784-612784

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.1501C>T; p.L501F; 11:612695-612695

 skinmalignant_melanomaSubstitution - Missense

c.861C>A; p.S287S; 11:613810-613810

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.401T>A; p.V134E; 11:614829-614829

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.568G>T; p.G190C; 11:614324-614324

 oesophaguscarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.28G>A; p.G10S; 11:615291-615291

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1398G>A; p.L466L; 11:612798-612798

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.791C>T; p.A264V; 11:613965-613965

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.791C>T; p.A264V; 11:613965-613965

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.791C>T; p.A264V; 11:613965-613965

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1053G>A; p.P351P; 11:613429-613429

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.574A>G; p.K192E; 11:614318-614318

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.961C>T; p.P321S; 11:613521-613521

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.766A>C; p.T256P; 11:613990-613990

 thyroidother; neoplasmSubstitution - Missense

c.216C>T; p.I72I; 11:615103-615103

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.1426G>C; p.E476Q; 11:612770-612770

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.1426G>C; p.E476Q; 11:612770-612770

 salivary_glandcarcinoma; adenoid_cystic_carcinomaSubstitution - Missense

c.136C>G; p.L46V; 11:615183-615183

 oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Missense

c.557C>A; p.P186H; 11:614335-614335

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.692T>A; p.L231H; 11:614200-614200

 oesophaguscarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1515C>T; p.I505I; 11:612681-612681

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.54C>A; p.T18T; 11:615265-615265

 livercarcinoma; hepatocellular_carcinomaSubstitution - coding silent

c.1128G>A; p.G376G; 11:613354-613354

 oesophaguscarcinoma; adenocarcinomaSubstitution - coding silent

c.1196C>A; p.S399Y; 11:613286-613286

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.325C>T; p.R109C; 11:614905-614905

 ovaryother; neoplasmSubstitution - Missense

c.325C>T; p.R109C; 11:614905-614905

 ovaryother; neoplasmSubstitution - Missense

c.305C>T; p.A102V; 11:614925-614925

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1018_1019insC; p.Q340fs*75; 11:613463-613464

 large_intestine; caecumcarcinoma; adenocarcinomaInsertion - Frameshift

c.501C>T; p.P167P; 11:614391-614391

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1318C>T; p.R440C; 11:613076-613076

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1331A>C; p.Y444S; 11:613063-613063

 thyroidother; neoplasmSubstitution - Missense

c.591C>T; p.L197L; 11:614301-614301

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.1192G>A; p.G398S; 11:613290-613290

 skinmalignant_melanomaSubstitution - Missense

c.1052C>T; p.P351L; 11:613430-613430

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.702_703delTG; p.A236fs*178; 11:614189-614190

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.787C>G; p.P263A; 11:613969-613969

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1213C>G; p.P405A; 11:613269-613269

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.38C>T; p.S13F; 11:615281-615281

 breastcarcinomaSubstitution - Missense

c.1479C>T; p.L493L; 11:612717-612717

 lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.1274A>G; p.Q425R; 11:613208-613208

 thyroidother; neoplasmSubstitution - Missense

c.518C>A; p.A173E; 11:614374-614374

 livercarcinomaSubstitution - Missense

c.105C>T; p.I35I; 11:615214-615214

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.385G>A; p.A129T; 11:614845-614845

 skin; extremitymalignant_melanomaSubstitution - Missense

c.70C>T; p.R24C; 11:615249-615249

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.461C>T; p.A154V; 11:614507-614507

 lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.551C>A; p.P184H; 11:614341-614341

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.593A>G; p.Q198R; 11:614299-614299

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1197C>T; p.S399S; 11:613285-613285

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1352T>C; p.L451P; 11:613042-613042

 livercarcinomaSubstitution - Missense

c.1480T>C; p.C494R; 11:612716-612716

 skinmalignant_melanomaSubstitution - Missense

c.1012G>T; p.D338Y; 11:613470-613470

 pancreascarcinomaSubstitution - Missense

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