| Gene ID | 56937 |
| Symbol | PMEPA1 |
| Synonymous | STAG1|TMEPAI |
| Full name | prostate transmembrane protein, androgen induced 1 |
| Gene description | prostate transmembrane protein androgen induced 1|protein TMEPAI|solid tumor-associated 1 protein|transmembrane, prostate androgen induced RNA |
| Cytoband | 20q13.31-q13.33 |
| Gene type | protein-coding |
| Synonymous | MIM:606564; HGNC:HGNC:14107; Ensembl:ENSG00000124225; HPRD:09415; Vega:OTTHUMG00000032831 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.680G>A; p.G227E; 20:57652237-57652237 |
skin | malignant_melanoma | Substitution - Missense |
c.436C>T; p.L146L; 20:57652481-57652481 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.552C>T; p.R184R; 20:57652365-57652365 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.552C>T; p.R184R; 20:57652365-57652365 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.459A>G; p.S153S; 20:57652458-57652458 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - coding silent |
c.459A>G; p.S153S; 20:57652458-57652458 |
thyroid | other; neoplasm | Substitution - coding silent |
c.174C>T; p.I58I; 20:57659633-57659633 |
skin | malignant_melanoma | Substitution - coding silent |
c.357G>A; p.L119L; 20:57652560-57652560 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.515C>T; p.P172L; 20:57652402-57652402 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.286G>C; p.E96Q; 20:57653065-57653065 |
breast | carcinoma | Substitution - Missense |
c.413C>T; p.P138L; 20:57652504-57652504 |
skin | malignant_melanoma | Substitution - Missense |
c.148G>A; p.V50M; 20:57659659-57659659 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.412C>T; p.P138S; 20:57652505-57652505 |
skin | malignant_melanoma | Substitution - Missense |
c.336G>A; p.P112P; 20:57652581-57652581 |
soft_tissue; striated_muscle | rhabdomyosarcoma | Substitution - coding silent |
c.791C>G; p.T264R; 20:57652126-57652126 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.632A>C; p.N211T; 20:57652285-57652285 |
prostate | carcinoma | Substitution - Missense |
c.593A>T; p.D198V; 20:57652324-57652324 |
breast | carcinoma | Substitution - Missense |
c.655T>C; p.Y219H; 20:57652262-57652262 |
liver | carcinoma | Substitution - Missense |
c.655T>C; p.Y219H; 20:57652262-57652262 |
liver | carcinoma | Substitution - Missense |
c.553G>A; p.A185T; 20:57652364-57652364 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.177G>A; p.T59T; 20:57659630-57659630 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.801G>A; p.A267A; 20:57652116-57652116 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.801G>A; p.A267A; 20:57652116-57652116 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.801G>A; p.A267A; 20:57652116-57652116 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.484C>T; p.Q162*; 20:57652433-57652433 |
skin | malignant_melanoma | Substitution - Nonsense |
c.59T>C; p.V20A; 20:57709524-57709524 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.837G>C; p.K279N; 20:57652080-57652080 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.671G>A; p.R224H; 20:57652246-57652246 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.492C>A; p.P164P; 20:57652425-57652425 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.850G>A; p.G284R; 20:57652067-57652067 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.479C>A; p.P160H; 20:57652438-57652438 |
kidney | carcinoma; renal_cell_carcinoma | Substitution - Missense |
c.384G>C; p.E128D; 20:57652533-57652533 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.789_790insCCAC; p.T264fs*19; 20:57652127-57652128 |
peritoneum; appendix | other; pseudomyxoma_peritonei | Insertion - Frameshift |
c.132C>T; p.I44I; 20:57659675-57659675 |
skin | malignant_melanoma | Substitution - coding silent |
c.390C>T; p.F130F; 20:57652527-57652527 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.390C>T; p.F130F; 20:57652527-57652527 |
skin | malignant_melanoma | Substitution - coding silent |
c.769G>T; p.E257*; 20:57652148-57652148 |
breast | carcinoma | Substitution - Nonsense |
c.580_585delAGTGAC; p.S194_D195delSD; 20:57652332-57652337 |
breast | carcinoma | Deletion - In frame |
c.650C>T; p.T217M; 20:57652267-57652267 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.501C>T; p.L167L; 20:57652416-57652416 |
skin | malignant_melanoma | Substitution - coding silent |
c.488G>A; p.G163D; 20:57652429-57652429 |
skin | malignant_melanoma | Substitution - Missense |
c.501C>T; p.L167L; 20:57652416-57652416 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.441A>G; p.P147P; 20:57652476-57652476 |
thyroid | other; neoplasm | Substitution - coding silent |
c.441A>G; p.P147P; 20:57652476-57652476 |
thyroid | other; neoplasm | Substitution - coding silent |
c.441A>G; p.P147P; 20:57652476-57652476 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.141C>T; p.I47I; 20:57659666-57659666 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.43G>A; p.A15T; 20:57709540-57709540 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.349G>A; p.D117N; 20:57652568-57652568 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.367C>A; p.P123T; 20:57652550-57652550 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.795_796delCA; p.I266fs*15; 20:57652121-57652122 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.828C>T; p.S276S; 20:57652089-57652089 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.296T>C; p.V99A; 20:57653055-57653055 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.480C>T; p.P160P; 20:57652437-57652437 |
skin | malignant_melanoma | Substitution - coding silent |
c.372C>T; p.F124F; 20:57652545-57652545 |
skin | malignant_melanoma | Substitution - coding silent |
c.497C>T; p.T166I; 20:57652420-57652420 |
pancreas | NS | Substitution - Missense |
c.464G>C; p.G155A; 20:57652453-57652453 |
skin | malignant_melanoma | Substitution - Missense |
c.573C>G; p.I191M; 20:57652344-57652344 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.264A>G; p.S88S; 20:57659543-57659543 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.772G>A; p.G258R; 20:57652145-57652145 |
skin | malignant_melanoma | Substitution - Missense |
c.605T>G; p.L202R; 20:57652312-57652312 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.508C>T; p.R170W; 20:57652409-57652409 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.670C>T; p.R224C; 20:57652247-57652247 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.852A>G; p.G284G; 20:57652065-57652065 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.624_625insC; p.S209fs*3; 20:57652292-57652293 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.624_625insC; p.S209fs*3; 20:57652292-57652293 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.624_625insC; p.S209fs*3; 20:57652292-57652293 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.624_625insC; p.S209fs*3; 20:57652292-57652293 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.522G>A; p.Q174Q; 20:57652395-57652395 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.814G>A; p.A272T; 20:57652103-57652103 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.624delC; p.S209fs*61; 20:57652293-57652293 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.624delC; p.S209fs*61; 20:57652293-57652293 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.624delC; p.S209fs*61; 20:57652293-57652293 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.624delC; p.S209fs*61; 20:57652293-57652293 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.636G>A; p.S212S; 20:57652281-57652281 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.624delC; p.S209fs*61; 20:57652293-57652293 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.624delC; p.S209fs*61; 20:57652293-57652293 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.624delC; p.S209fs*61; 20:57652293-57652293 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.386G>A; p.R129H; 20:57652531-57652531 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.698G>A; p.S233N; 20:57652219-57652219 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.433G>A; p.D145N; 20:57652484-57652484 |
skin | malignant_melanoma | Substitution - Missense |
c.433G>A; p.D145N; 20:57652484-57652484 |
skin | malignant_melanoma | Substitution - Missense |