| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 55281 |
Name | TMEM140 |
Synonymous | transmembrane protein 140;TMEM140;transmembrane protein 140 |
Definition | - |
Position | 7q33 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.359T>G; p.L120R; 7:135164800-135164800 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - Missense |
c.240G>A; p.L80L; 7:135164681-135164681 |
bone; pelvis | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.310G>C; p.A104P; 7:135164751-135164751 |
breast | carcinoma | Substitution - Missense |
c.219G>C; p.L73L; 7:135164660-135164660 |
breast | carcinoma | Substitution - coding silent |
c.5C>T; p.A2V; 7:135164446-135164446 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.26G>A; p.R9H; 7:135164467-135164467 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.362C>A; p.A121D; 7:135164803-135164803 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.480A>G; p.L160L; 7:135164921-135164921 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.335C>A; p.A112E; 7:135164776-135164776 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.290delC; p.Q99fs*5; 7:135164731-135164731 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.290delC; p.Q99fs*5; 7:135164731-135164731 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.5C>T; p.A2V; 7:135164446-135164446 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.5C>T; p.A2V; 7:135164446-135164446 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.5C>T; p.A2V; 7:135164446-135164446 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.333_334delAG; p.R111fs*65; 7:135164774-135164775 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.7G>A; p.G3S; 7:135164448-135164448 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.388G>A; p.G130S; 7:135164829-135164829 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.25C>T; p.R9C; 7:135164466-135164466 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.236G>A; p.G79D; 7:135164677-135164677 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.441G>A; p.P147P; 7:135164882-135164882 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.328_329delGA; p.R111fs*65; 7:135164769-135164770 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.203_204insT; p.E69fs*1; 7:135164644-135164645 |
lung | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.537G>C; p.E179D; 7:135164978-135164978 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.299C>T; p.P100L; 7:135164740-135164740 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.193C>G; p.H65D; 7:135164634-135164634 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.291C>A; p.A97A; 7:135164732-135164732 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.229C>A; p.R77R; 7:135164670-135164670 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.383C>T; p.A128V; 7:135164824-135164824 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.83T>C; p.M28T; 7:135164524-135164524 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.299C>A; p.P100H; 7:135164740-135164740 |
ovary | other; neoplasm | Substitution - Missense |
c.299C>A; p.P100H; 7:135164740-135164740 |
ovary | other; neoplasm | Substitution - Missense |
c.342G>A; p.R114R; 7:135164783-135164783 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.248C>T; p.A83V; 7:135164689-135164689 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.149A>G; p.Y50C; 7:135164590-135164590 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.110G>A; p.G37D; 7:135164551-135164551 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.74T>C; p.I25T; 7:135164515-135164515 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.384A>C; p.A128A; 7:135164825-135164825 |
thyroid | other; neoplasm | Substitution - coding silent |
c.547G>A; p.E183K; 7:135164988-135164988 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.75C>T; p.I25I; 7:135164516-135164516 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.75C>T; p.I25I; 7:135164516-135164516 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.211G>A; p.E71K; 7:135164652-135164652 |
urinary_tract; bladder | carcinoma | Substitution - Missense |