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Gene information | Literature | Expression | lncRNA | Mutation | Homolog

Basic Information

Gene ID

2253

Name

FGF8

Synonymous

fibroblast growth factor 8 (androgen-induced);FGF8;fibroblast growth factor 8 (androgen-induced)

Definition

androgen-induced growth factor|fibroblast growth factor 8|heparin-binding growth factor 8

Position

10q24

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.583C>T; p.R195W; 10:101770481-101770481

 breastcarcinomaSubstitution - Missense

c.273G>A; p.G91G; 10:101774796-101774796

 breastcarcinomaSubstitution - coding silent

c.255C>G; p.L85L; 10:101774814-101774814

 breastcarcinomaSubstitution - coding silent

c.676C>T; p.P226S; 10:101770388-101770388

 breastcarcinomaSubstitution - Missense

c.469G>A; p.V157I; 10:101770595-101770595

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.92C>T; p.A31V; 10:101775194-101775194

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.158T>G; p.V53G; 10:101774911-101774911

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.309C>A; p.N103K; 10:101774760-101774760

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.413G>A; p.C138Y; 10:101771494-101771494

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.324C>T; p.D108D; 10:101774745-101774745

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.170C>T; p.S57F; 10:101774899-101774899

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.202C>T; p.Q68*; 10:101774867-101774867

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.202C>T; p.Q68*; 10:101774867-101774867

 large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.302G>A; p.R101H; 10:101774767-101774767

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.625C>T; p.R209W; 10:101770439-101770439

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.217G>A; p.D73N; 10:101774852-101774852

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.106C>A; p.L36I; 10:101775180-101775180

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.616C>T; p.R206W; 10:101770448-101770448

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.385C>T; p.R129*; 10:101771522-101771522

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.703A>G; p.S235G; 10:101770361-101770361

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.686C>T; p.T229M; 10:101770378-101770378

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.410T>C; p.I137T; 10:101771497-101771497

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.581C>T; p.T194M; 10:101770483-101770483

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.325G>A; p.G109S; 10:101774744-101774744

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.730C>T; p.R244*; 10:101770334-101770334

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.379C>T; p.R127*; 10:101771528-101771528

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.346A>G; p.I116V; 10:101771561-101771561

 livercarcinomaSubstitution - Missense

c.526G>A; p.E176K; 10:101770538-101770538

 lung; middle_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.386G>A; p.R129Q; 10:101771521-101771521

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.310G>A; p.A104T; 10:101774759-101774759

 lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.279C>G; p.H93Q; 10:101774790-101774790

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.195G>C; p.V65V; 10:101774874-101774874

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.526G>A; p.E176K; 10:101770538-101770538

 oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.581C>T; p.T194M; 10:101770483-101770483

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.609C>T; p.F203F; 10:101770455-101770455

 skinmalignant_melanomaSubstitution - coding silent

c.506C>T; p.A169V; 10:101770558-101770558

 skinmalignant_melanomaSubstitution - Missense

c.332C>T; p.P111L; 10:101774737-101774737

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.444+2T>C; p.?; 10:101771461-101771461

 stomachcarcinoma; adenocarcinomaUnknown

c.608T>G; p.F203C; 10:101770456-101770456

 stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.417G>A; p.M139I; 10:101771490-101771490

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.225C>G; p.L75L; 10:101774844-101774844

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.411C>G; p.I137M; 10:101771496-101771496

 urinary_tract; bladdercarcinomaSubstitution - Missense