| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 10971 |
Name | YWHAQ |
Synonymous | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, theta;YWHAQ;tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, theta |
Definition | 14-3-3 protein T-cell|14-3-3 protein tau|14-3-3 protein theta|tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, theta polypeptide |
Position | 2p25.1 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.474A>G; p.K158K; 2:9588273-9588273 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.536A>G; p.Y179C; 2:9588211-9588211 |
breast | carcinoma; ER-PR-positive_carcinoma | Substitution - Missense |
c.232C>T; p.L78L; 2:9630221-9630221 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.252G>T; p.E84D; 2:9630201-9630201 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.191G>A; p.S64N; 2:9630262-9630262 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.664A>G; p.R222G; 2:9587428-9587428 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - Missense |
c.90C>G; p.T30T; 2:9630363-9630363 |
kidney | other; neoplasm | Substitution - coding silent |
c.81G>A; p.K27K; 2:9630372-9630372 |
kidney | other; neoplasm | Substitution - coding silent |
c.84A>C; p.A28A; 2:9630369-9630369 |
kidney | other; neoplasm | Substitution - coding silent |
c.439G>T; p.G147*; 2:9588308-9588308 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.419-1G>T; p.?; 2:9588329-9588329 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.362T>C; p.M121T; 2:9591448-9591448 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.319G>T; p.A107S; 2:9591491-9591491 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.564C>A; p.A188A; 2:9588183-9588183 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.587T>G; p.F196C; 2:9587505-9587505 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.295-2A>G; p.?; 2:9591517-9591517 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.69C>T; p.A23A; 2:9630384-9630384 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.616C>G; p.L206V; 2:9587476-9587476 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.423G>A; p.T141T; 2:9588324-9588324 |
liver | carcinoma | Substitution - coding silent |
c.583-5A>T; p.?; 2:9587514-9587514 |
liver | carcinoma | Unknown |
c.583-5A>T; p.?; 2:9587514-9587514 |
liver | carcinoma | Unknown |
c.195C>G; p.I65M; 2:9630258-9630258 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.170C>T; p.S57F; 2:9630283-9630283 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.221A>G; p.K74R; 2:9630232-9630232 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.287C>T; p.T96M; 2:9630166-9630166 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.183C>T; p.V61V; 2:9630270-9630270 |
pancreas | carcinoma | Substitution - coding silent |
c.135C>T; p.S45S; 2:9630318-9630318 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.440G>A; p.G147E; 2:9588307-9588307 |
skin | malignant_melanoma | Substitution - Missense |
c.582+1G>A; p.?; 2:9588164-9588164 |
skin | malignant_melanoma | Unknown |
c.650T>G; p.I217S; 2:9587442-9587442 |
skin | malignant_melanoma | Substitution - Missense |
c.627C>T; p.D209D; 2:9587465-9587465 |
skin | malignant_melanoma | Substitution - coding silent |
c.499C>T; p.R167C; 2:9588248-9588248 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.671A>G; p.N224S; 2:9587421-9587421 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.564C>T; p.A188A; 2:9588183-9588183 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.295-1G>T; p.?; 2:9591516-9591516 |
stomach | carcinoma; intestinal_adenocarcinoma | Unknown |
c.574G>A; p.A192T; 2:9588173-9588173 |
urinary_tract; bladder | carcinoma | Substitution - Missense |