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

Basic Information

Gene ID

2247

Name

FGF2

Synonymous

fibroblast growth factor 2 (basic);FGF2;fibroblast growth factor 2 (basic)

Definition

basic fibroblast growth factor bFGF|fibroblast growth factor 2|heparin-binding growth factor 2|prostatropin

Position

4q26

Gene Type

protein-coding

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.477C>G; p.F159L; 4:122827252-122827252

cervixcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.620T>C; p.I207T; 4:122876363-122876363

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.529C>A; p.H177N; 4:122827304-122827304

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.155C>A; p.S52Y; 4:122826930-122826930

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.645C>A; p.Y215*; 4:122876388-122876388

lungcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.4G>A; p.V2M; 4:122826779-122826779

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.12delG; p.G6fs*4; 4:122826787-122826787

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.519C>T; p.F173F; 4:122827294-122827294

skinmalignant_melanomaSubstitution - coding silent

c.77delC; p.R27fs*27; 4:122826852-122826852

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.715C>T; p.R239*; 4:122892244-122892244

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.715C>T; p.R239*; 4:122892244-122892244

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.864C>T; p.S288S; 4:122892393-122892393

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.862A>G; p.S288G; 4:122892391-122892391

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.862A>G; p.S288G; 4:122892391-122892391

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.770A>T; p.Y257F; 4:122892299-122892299

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.530A>C; p.H177P; 4:122827305-122827305

pancreascarcinomaSubstitution - Missense

c.746G>A; p.R249Q; 4:122892275-122892275

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.744C>A; p.Y248*; 4:122892273-122892273

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Nonsense

c.826C>A; p.Q276K; 4:122892355-122892355

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.619A>G; p.I207V; 4:122876362-122876362

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.407C>T; p.A136V; 4:122827182-122827182

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.12G>C; p.V4V; 4:122826787-122826787

thyroidother; neoplasmSubstitution - coding silent

c.499T>A; p.C167S; 4:122827274-122827274

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.210A>G; p.T70T; 4:122826985-122826985

pancreascarcinomaSubstitution - coding silent

c.485C>T; p.P162L; 4:122827260-122827260

skin; extremitymalignant_melanomaSubstitution - Missense

c.661G>A; p.D221N; 4:122876404-122876404

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.645C>T; p.Y215Y; 4:122876388-122876388

pancreascarcinomaSubstitution - coding silent

c.531delC; p.D179fs*40; 4:122827306-122827306

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.523C>T; p.R175C; 4:122827298-122827298

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.785G>A; p.R262Q; 4:122892314-122892314

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.785G>A; p.R262Q; 4:122892314-122892314

skinmalignant_melanomaSubstitution - Missense

c.156C>T; p.S52S; 4:122826931-122826931

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.156C>T; p.S52S; 4:122826931-122826931

thyroidother; neoplasmSubstitution - coding silent

c.654G>C; p.M218I; 4:122876397-122876397

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.864C>G; p.S288R; 4:122892393-122892393

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.861G>A; p.K287K; 4:122892390-122892390

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.157G>A; p.V53M; 4:122826932-122826932

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense


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