| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 7532 |
Name | YWHAG |
Synonymous | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma;YWHAG;tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma |
Definition | 14-3-3 gamma|14-3-3 protein gamma|KCIP-1|protein kinase C inhibitor protein 1|protein phosphatase 1, regulatory subunit 170|tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide |
Position | 7q11.23 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.137C>G; p.S46C; 7:76330184-76330184 |
breast | carcinoma | Substitution - Missense |
c.252G>A; p.A84A; 7:76330069-76330069 |
breast | carcinoma | Substitution - coding silent |
c.170G>A; p.R57H; 7:76330151-76330151 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.607G>A; p.D203N; 7:76329714-76329714 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.597C>T; p.T199T; 7:76329724-76329724 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.619G>A; p.E207K; 7:76329702-76329702 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.450C>T; p.S150S; 7:76329871-76329871 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.541G>T; p.V181F; 7:76329780-76329780 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.604G>A; p.D202N; 7:76329717-76329717 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.540C>T; p.S180S; 7:76329781-76329781 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.125G>A; p.R42Q; 7:76330196-76330196 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.171C>A; p.R57R; 7:76330150-76330150 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.660G>A; p.T220T; 7:76329661-76329661 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.616G>A; p.A206T; 7:76329705-76329705 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.330G>T; p.K110N; 7:76329991-76329991 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.153C>T; p.N51N; 7:76330168-76330168 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.505_506insC; p.H169fs*10; 7:76329815-76329816 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.729C>T; p.G243G; 7:76329592-76329592 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.594G>A; p.K198K; 7:76329727-76329727 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.597C>T; p.T199T; 7:76329724-76329724 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.340G>A; p.E114K; 7:76329981-76329981 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.485A>T; p.K162I; 7:76329836-76329836 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.113C>T; p.S38L; 7:76330208-76330208 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.26A>G; p.Q9R; 7:76358783-76358783 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.480C>T; p.I160I; 7:76329841-76329841 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.692C>T; p.T231M; 7:76329629-76329629 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.434C>T; p.T145M; 7:76329887-76329887 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.288_289GT>AA; p.C97S; 7:76330032-76330033 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.169C>T; p.R57C; 7:76330152-76330152 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.666C>A; p.I222I; 7:76329655-76329655 |
prostate | carcinoma | Substitution - coding silent |
c.522C>T; p.G174G; 7:76329799-76329799 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.348G>A; p.Q116Q; 7:76329973-76329973 |
skin | malignant_melanoma | Substitution - coding silent |
c.432G>T; p.A144A; 7:76329889-76329889 |
skin | malignant_melanoma | Substitution - coding silent |
c.258_259GG>AA; p.E87K; 7:76330062-76330063 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.230A>G; p.K77R; 7:76330091-76330091 |
skin | malignant_melanoma | Substitution - Missense |
c.615C>T; p.I205I; 7:76329706-76329706 |
skin | malignant_melanoma | Substitution - coding silent |
c.427A>G; p.R143G; 7:76329894-76329894 |
skin | malignant_melanoma | Substitution - Missense |
c.154G>A; p.V52I; 7:76330167-76330167 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.201G>A; p.E67E; 7:76330120-76330120 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.418G>T; p.G140*; 7:76329903-76329903 |
thyroid | carcinoma | Substitution - Nonsense |
c.378G>A; p.M126I; 7:76329943-76329943 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - Missense |
c.378G>A; p.M126I; 7:76329943-76329943 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.295G>A; p.D99N; 7:76330026-76330026 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.295G>A; p.D99N; 7:76330026-76330026 |
urinary_tract; bladder | carcinoma | Substitution - Missense |