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

Basic Information

Gene ID

3087

Name

HHEX

Synonymous

hematopoietically expressed homeobox;HHEX;hematopoietically expressed homeobox

Definition

hematopoietically-expressed homeobox protein HHEX|homeobox protein HEX|homeobox protein PRH|homeobox, hematopoietically expressed|proline-rich homeodomain-containing transcription factor

Position

10q23.33

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.786C>T; p.G262G; 10:92694741-92694741

 bone; extraskeletalEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.372A>C; p.L124L; 10:92692378-92692378

 breastcarcinomaSubstitution - coding silent

c.718C>G; p.P240A; 10:92694673-92694673

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.592G>T; p.E198*; 10:92694547-92694547

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.616G>T; p.E206*; 10:92694571-92694571

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.410G>T; p.R137M; 10:92692416-92692416

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.786C>T; p.G262G; 10:92694741-92694741

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.468C>T; p.F156F; 10:92692474-92692474

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.619G>T; p.E207*; 10:92694574-92694574

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.747G>T; p.E249D; 10:92694702-92694702

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.622C>G; p.L208V; 10:92694577-92694577

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.722C>A; p.A241D; 10:92694677-92694677

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.484C>A; p.L162I; 10:92692490-92692490

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.792A>C; p.K264N; 10:92694747-92694747

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.473C>T; p.T158M; 10:92692479-92692479

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.667A>G; p.S223G; 10:92694622-92694622

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.749T>C; p.I250T; 10:92694704-92694704

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.624delG; p.E209fs*>62; 10:92694579-92694579

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.564A>G; p.R188R; 10:92692725-92692725

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.474G>A; p.T158T; 10:92692480-92692480

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.418G>A; p.G140S; 10:92692424-92692424

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.794G>T; p.S265I; 10:92694749-92694749

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.483_484delTC; p.P164fs*27; 10:92692489-92692490

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.404A>G; p.H135R; 10:92692410-92692410

 livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.201C>T; p.T67T; 10:92690187-92690187

 livercarcinomaSubstitution - coding silent

c.201C>T; p.T67T; 10:92690187-92690187

 livercarcinomaSubstitution - coding silent

c.747G>T; p.E249D; 10:92694702-92694702

 livercarcinomaSubstitution - Missense

c.400C>G; p.L134V; 10:92692406-92692406

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.565C>T; p.R189C; 10:92692726-92692726

 lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.803A>G; p.N268S; 10:92694758-92694758

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.515A>T; p.K172M; 10:92692521-92692521

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.375C>G; p.L125L; 10:92692381-92692381

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.375C>G; p.L125L; 10:92692381-92692381

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.556C>T; p.Q186*; 10:92692717-92692717

 lungcarcinoma; small_cell_carcinomaSubstitution - Nonsense

c.278C>T; p.P93L; 10:92690264-92690264

 ovaryother; neoplasmSubstitution - Missense

c.748A>G; p.I250V; 10:92694703-92694703

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.726C>T; p.S242S; 10:92694681-92694681

 skinmalignant_melanomaSubstitution - coding silent

c.446C>T; p.T149I; 10:92692452-92692452

 skinmalignant_melanomaSubstitution - Missense

c.171C>T; p.S57S; 10:92690157-92690157

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.724T>A; p.S242T; 10:92694679-92694679

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.556C>T; p.Q186*; 10:92692717-92692717

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.346C>T; p.R116C; 10:92690332-92690332

 skinmalignant_melanomaSubstitution - Missense

c.451G>A; p.E151K; 10:92692457-92692457

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.450C>T; p.I150I; 10:92692456-92692456

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.468C>T; p.F156F; 10:92692474-92692474

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.496G>A; p.E166K; 10:92692502-92692502

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.496G>A; p.E166K; 10:92692502-92692502

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.274G>A; p.G92R; 10:92690260-92690260

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.275G>T; p.G92V; 10:92690261-92690261

 urinary_tract; bladdercarcinomaSubstitution - Missense