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

Basic Information

Gene ID

3925

Name

STMN1

Synonymous

stathmin 1;STMN1;stathmin 1

Definition

leukemia-associated phosphoprotein p18|metablastin|oncoprotein 18|phosphoprotein 19|phosphoprotein p19|prosolin|stathmin|stathmin 1/oncoprotein 18|transmembrane protein C1orf215

Position

1p36.11

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.226C>T; p.R76*; 1:25901643-25901643

 breastcarcinoma; basal_(triple-negative)_carcinomaSubstitution - Nonsense

c.279C>T; p.F93F; 1:25901590-25901590

 breastcarcinomaSubstitution - coding silent

c.91T>C; p.S31P; 1:25903736-25903736

 central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaSubstitution - Missense

c.248T>C; p.L83P; 1:25901621-25901621

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.88G>T; p.E30*; 1:25903739-25903739

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.437C>A; p.T146N; 1:25901029-25901029

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.450A>C; p.*150Y; 1:25901016-25901016

 endometriumcarcinoma; endometrioid_carcinomaNonstop extension

c.92C>A; p.S31Y; 1:25903735-25903735

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.234C>T; p.H78H; 1:25901635-25901635

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.220G>A; p.E74K; 1:25901649-25901649

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.40C>T; p.R14C; 1:25903787-25903787

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.172G>T; p.E58*; 1:25903655-25903655

 large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.274_276delAAC; p.N92delN; 1:25901593-25901595

 large_intestine; rectumcarcinoma; adenocarcinomaDeletion - In frame

c.226C>T; p.R76*; 1:25901643-25901643

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.412G>T; p.E138*; 1:25901054-25901054

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.412G>T; p.E138*; 1:25901054-25901054

 large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.28G>T; p.E10*; 1:25903799-25903799

 large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.370C>T; p.R124*; 1:25901499-25901499

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.19C>T; p.Q7*; 1:25903808-25903808

 livercarcinomaSubstitution - Nonsense

c.19C>T; p.Q7*; 1:25903808-25903808

 livercarcinomaSubstitution - Nonsense

c.130G>A; p.D44N; 1:25903697-25903697

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.265G>T; p.E89*; 1:25901604-25901604

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Nonsense

c.52C>G; p.Q18E; 1:25903775-25903775

 oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Missense

c.88G>C; p.E30Q; 1:25903739-25903739

 ovaryother; neoplasmSubstitution - Missense

c.187-6T>G; p.?; 1:25901688-25901688

 ovaryother; neoplasmUnknown

c.187-6T>G; p.?; 1:25901688-25901688

 ovaryother; neoplasmUnknown

c.189C>T; p.S63S; 1:25901680-25901680

 skin; legmalignant_melanoma; nodularSubstitution - coding silent

c.140T>G; p.L47R; 1:25903687-25903687

 skinmalignant_melanomaSubstitution - Missense

c.115C>T; p.P39S; 1:25903712-25903712

 skinmalignant_melanomaSubstitution - Missense

c.377A>G; p.K126R; 1:25901492-25901492

 skinmalignant_melanomaSubstitution - Missense

c.188C>T; p.S63F; 1:25901681-25901681

 skin; legmalignant_melanoma; nodularSubstitution - Missense

c.187T>C; p.S63P; 1:25901682-25901682

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.182G>A; p.R61H; 1:25903645-25903645

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.70C>T; p.L24F; 1:25903757-25903757

 urinary_tract; bladdercarcinomaSubstitution - Missense