| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 6760 |
Name | SS18 |
Synonymous | synovial sarcoma translocation, chromosome 18;SS18;synovial sarcoma translocation, chromosome 18 |
Definition | protein SSXT|synovial sarcoma translocated to X chromosome protein|synovial sarcoma, translocated to X chromosome |
Position | 18q11.2 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.563G>T; p.G188V; 18:26052668-26052668 |
adrenal_gland; adrenal_gland | adrenal_cortical_carcinoma; functioning | Substitution - Missense |
c.635C>G; p.S212C; 18:26039429-26039429 |
breast | carcinoma | Substitution - Missense |
c.607+6T>C; p.?; 18:26052618-26052618 |
breast | carcinoma; ductal_carcinoma | Unknown |
c.199T>A; p.S67T; 18:26078108-26078108 |
breast | carcinoma | Substitution - Missense |
c.236C>A; p.P79H; 18:26057738-26057738 |
breast | carcinoma | Substitution - Missense |
c.637C>G; p.Q213E; 18:26039427-26039427 |
breast | carcinoma | Substitution - Missense |
c.872A>C; p.Y291S; 18:26038563-26038563 |
breast | carcinoma | Substitution - Missense |
c.1113T>C; p.G371G; 18:26032516-26032516 |
breast | carcinoma | Substitution - coding silent |
c.815G>A; p.G272E; 18:26038620-26038620 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1165G>T; p.G389*; 18:26032464-26032464 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.131C>T; p.T44I; 18:26087516-26087516 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.52C>T; p.P18S; 18:26090518-26090518 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.330A>T; p.V110V; 18:26057644-26057644 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.51T>C; p.T17T; 18:26090519-26090519 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.730A>G; p.M244V; 18:26039334-26039334 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1096+2T>C; p.?; 18:26035003-26035003 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Unknown |
c.136G>A; p.E46K; 18:26087511-26087511 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.298C>T; p.R100C; 18:26057676-26057676 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.502C>T; p.P168S; 18:26052729-26052729 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.502C>T; p.P168S; 18:26052729-26052729 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.502C>T; p.P168S; 18:26052729-26052729 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.930C>T; p.Y310Y; 18:26035874-26035874 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.450G>T; p.M150I; 18:26052781-26052781 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.338delG; p.G113fs*11; 18:26057636-26057636 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.886A>C; p.N296H; 18:26035918-26035918 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1149A>T; p.Q383H; 18:26032480-26032480 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.654A>G; p.P218P; 18:26039410-26039410 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.83A>G; p.N28S; 18:26087564-26087564 |
liver | carcinoma | Substitution - Missense |
c.83A>G; p.N28S; 18:26087564-26087564 |
liver | carcinoma | Substitution - Missense |
c.822A>G; p.Q274Q; 18:26038613-26038613 |
liver | carcinoma | Substitution - coding silent |
c.822A>G; p.Q274Q; 18:26038613-26038613 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.1165G>A; p.G389R; 18:26032464-26032464 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1077A>T; p.P359P; 18:26035024-26035024 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1198C>T; p.P400S; 18:26032431-26032431 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.694A>G; p.M232V; 18:26039370-26039370 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1167A>G; p.G389G; 18:26032462-26032462 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1029G>T; p.Q343H; 18:26035072-26035072 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.644A>T; p.Y215F; 18:26039420-26039420 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1197G>T; p.Q399H; 18:26032432-26032432 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.637C>G; p.Q213E; 18:26039427-26039427 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.872A>T; p.Y291F; 18:26038563-26038563 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.134C>T; p.S45L; 18:26087513-26087513 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.115C>T; p.Q39*; 18:26087532-26087532 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.663C>G; p.G221G; 18:26039401-26039401 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.27G>T; p.R9S; 18:26090543-26090543 |
oesophagus | carcinoma | Substitution - Missense |
c.109G>T; p.D37Y; 18:26087538-26087538 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1116A>G; p.P372P; 18:26032513-26032513 |
ovary | other; neoplasm | Substitution - coding silent |
c.702G>A; p.M234I; 18:26039362-26039362 |
pancreas | carcinoma | Substitution - Missense |
c.992A>C; p.Q331P; 18:26035109-26035109 |
pancreas | carcinoma | Substitution - Missense |
c.1217A>C; p.Y406S; 18:26032412-26032412 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1131T>C; p.P377P; 18:26032498-26032498 |
skin | malignant_melanoma | Substitution - coding silent |
c.1021C>T; p.P341S; 18:26035080-26035080 |
skin | malignant_melanoma | Substitution - Missense |
c.1021C>T; p.P341S; 18:26035080-26035080 |
skin | malignant_melanoma | Substitution - Missense |
c.758A>G; p.Y253C; 18:26039306-26039306 |
skin | malignant_melanoma | Substitution - Missense |
c.1214C>T; p.P405L; 18:26032415-26032415 |
skin | malignant_melanoma | Substitution - Missense |
c.1022C>T; p.P341L; 18:26035079-26035079 |
skin | malignant_melanoma | Substitution - Missense |
c.299G>A; p.R100H; 18:26057675-26057675 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.350C>T; p.P117L; 18:26057624-26057624 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.225_226insT; p.P76fs*56; 18:26078081-26078082 |
stomach | carcinoma; intestinal_adenocarcinoma | Insertion - Frameshift |
c.1093T>C; p.Y365H; 18:26035008-26035008 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.428T>A; p.L143H; 18:26052803-26052803 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.986A>C; p.Y329S; 18:26035115-26035115 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.369G>A; p.M123I; 18:26057605-26057605 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1119T>A; p.G373G; 18:26032510-26032510 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.769C>A; p.Q257K; 18:26039295-26039295 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.378G>C; p.Q126H; 18:26057596-26057596 |
urinary_tract; bladder | carcinoma | Substitution - Missense |