| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 10232 | ||
Name | MSLN | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.292A>G; p.T98A; 16:764135-764135 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.1352C>A; p.S451Y; 16:766765-766765 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.20G>A; p.R7Q; 16:762700-762700 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1809G>A; p.E603E; 16:768649-768649 |
skin | malignant_melanoma | Substitution - coding silent |
c.354C>T; p.L118L; 16:764700-764700 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.395C>T; p.S132L; 16:764921-764921 |
haematopoietic_and_lymphoid_tissue; skin | lymphoid_neoplasm; follicular_lymphoma | Substitution - Missense |
c.395C>T; p.S132L; 16:764921-764921 |
haematopoietic_and_lymphoid_tissue; abdomen | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.1179G>T; p.E393D; 16:766439-766439 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.29T>C; p.L10S; 16:762709-762709 |
skin | malignant_melanoma | Substitution - Missense |
c.925C>T; p.R309C; 16:766088-766088 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.925C>T; p.R309C; 16:766088-766088 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1837G>A; p.G613R; 16:768677-768677 |
skin; trunk | malignant_melanoma; nodular | Substitution - Missense |
c.1108C>T; p.Q370*; 16:766368-766368 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1531G>A; p.A511T; 16:767381-767381 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1860C>T; p.V620V; 16:768700-768700 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.466G>T; p.A156S; 16:764992-764992 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.571G>A; p.D191N; 16:765170-765170 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1490G>A; p.G497E; 16:766977-766977 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.341A>T; p.D114V; 16:764687-764687 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1257G>A; p.V419V; 16:766670-766670 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.461delG; p.A156fs*22; 16:764987-764987 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.461delG; p.A156fs*22; 16:764987-764987 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.23_24CC>TT; p.P8L; 16:762703-762704 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.111G>T; p.L37L; 16:763258-763258 |
kidney | other; neoplasm | Substitution - coding silent |
c.570C>T; p.C190C; 16:765169-765169 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.870G>T; p.R290R; 16:765765-765765 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1362C>G; p.P454P; 16:766775-766775 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.185C>T; p.S62F; 16:764028-764028 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Missense |
c.23C>A; p.P8H; 16:762703-762703 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1826C>A; p.P609H; 16:768666-768666 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; polycythaemia_vera | Substitution - Missense |
c.1433C>T; p.P478L; 16:766920-766920 |
breast | carcinoma | Substitution - Missense |
c.44C>T; p.T15I; 16:762724-762724 |
skin | malignant_melanoma | Substitution - Missense |
c.1557C>T; p.L519L; 16:767407-767407 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1447G>A; p.V483I; 16:766934-766934 |
skin | malignant_melanoma | Substitution - Missense |
c.705-2A>T; p.?; 16:765525-765525 |
lung | carcinoma; adenocarcinoma | Unknown |
c.176C>T; p.S59F; 16:763688-763688 |
skin; face | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.148G>A; p.G50R; 16:763660-763660 |
breast | carcinoma | Substitution - Missense |
c.1512C>T; p.I504I; 16:766999-766999 |
skin | malignant_melanoma | Substitution - coding silent |
c.767G>C; p.G256A; 16:765589-765589 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.867C>T; p.L289L; 16:765762-765762 |
skin | malignant_melanoma | Substitution - coding silent |
c.714G>A; p.S238S; 16:765536-765536 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.714G>A; p.S238S; 16:765536-765536 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1858G>A; p.V620I; 16:768698-768698 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1248C>T; p.L416L; 16:766661-766661 |
breast | carcinoma | Substitution - coding silent |
c.1801A>G; p.M601V; 16:768559-768559 |
thyroid | other; neoplasm | Substitution - Missense |
c.1586C>T; p.A529V; 16:767436-767436 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1801A>G; p.M601V; 16:768559-768559 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1801A>G; p.M601V; 16:768559-768559 |
breast | carcinoma | Substitution - Missense |
c.827C>T; p.S276F; 16:765722-765722 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1306G>A; p.D436N; 16:766719-766719 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.166C>G; p.P56A; 16:763678-763678 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1238G>A; p.R413Q; 16:766651-766651 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.149G>A; p.G50E; 16:763661-763661 |
skin | malignant_melanoma | Substitution - Missense |
c.1517C>T; p.S506F; 16:767004-767004 |
skin | malignant_melanoma | Substitution - Missense |
c.320G>A; p.R107Q; 16:764666-764666 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1326C>T; p.T442T; 16:766739-766739 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.138G>A; p.A46A; 16:763650-763650 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1538C>T; p.T513M; 16:767388-767388 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.682C>A; p.Q228K; 16:765281-765281 |
liver | carcinoma | Substitution - Missense |
c.1466G>A; p.R489H; 16:766953-766953 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.269C>A; p.A90E; 16:764112-764112 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1596G>C; p.M532I; 16:767446-767446 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.636G>A; p.P212P; 16:765235-765235 |
pancreas | NS | Substitution - coding silent |
c.1226C>A; p.P409H; 16:766486-766486 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1035C>T; p.T345T; 16:766198-766198 |
liver | carcinoma | Substitution - coding silent |
c.330_331insC; p.E113fs*69; 16:764676-764677 |
liver | carcinoma | Insertion - Frameshift |
c.54C>T; p.L18L; 16:762734-762734 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - coding silent |
c.1694G>A; p.R565H; 16:768452-768452 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Missense |
c.54C>T; p.L18L; 16:762734-762734 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1215C>T; p.H405H; 16:766475-766475 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1216G>A; p.E406K; 16:766476-766476 |
skin; face | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.883C>T; p.R295W; 16:765778-765778 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.801C>T; p.I267I; 16:765696-765696 |
skin | malignant_melanoma | Substitution - coding silent |
c.349G>A; p.A117T; 16:764695-764695 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1509G>T; p.K503N; 16:766996-766996 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.820C>T; p.R274C; 16:765715-765715 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.820C>T; p.R274C; 16:765715-765715 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.310C>G; p.L104V; 16:764656-764656 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1401G>T; p.A467A; 16:766888-766888 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.242G>A; p.R81H; 16:764085-764085 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1607C>G; p.T536R; 16:767457-767457 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.839C>A; p.S280Y; 16:765734-765734 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1377C>T; p.S459S; 16:766790-766790 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.435G>A; p.T145T; 16:764961-764961 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.1638G>A; p.E546E; 16:768396-768396 |
skin | malignant_melanoma | Substitution - coding silent |
c.795+1G>A; p.?; 16:765618-765618 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Unknown |
c.758C>T; p.P253L; 16:765580-765580 |
skin | malignant_melanoma | Substitution - Missense |
c.1717C>T; p.R573W; 16:768475-768475 |
ovary | other; neoplasm | Substitution - Missense |
c.1154G>A; p.R385H; 16:766414-766414 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.936C>T; p.D312D; 16:766099-766099 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.59G>A; p.S20N; 16:762739-762739 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.885G>A; p.R295R; 16:765780-765780 |
skin | malignant_melanoma | Substitution - coding silent |
c.738C>T; p.D246D; 16:765560-765560 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1236T>C; p.P412P; 16:766649-766649 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.531G>A; p.L177L; 16:765130-765130 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1608G>T; p.T536T; 16:767458-767458 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1340G>T; p.G447V; 16:766753-766753 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.375C>T; p.F125F; 16:764721-764721 |
skin | malignant_melanoma | Substitution - coding silent |
c.1494C>T; p.S498S; 16:766981-766981 |
ovary | other; neoplasm | Substitution - coding silent |
c.829C>A; p.R277R; 16:765724-765724 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.857G>A; p.R286Q; 16:765752-765752 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.227G>A; p.G76D; 16:764070-764070 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.928G>T; p.E310*; 16:766091-766091 |
liver | carcinoma | Substitution - Nonsense |
c.928G>T; p.E310*; 16:766091-766091 |
liver | carcinoma | Substitution - Nonsense |
c.1020C>T; p.N340N; 16:766183-766183 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.638G>A; p.G213E; 16:765237-765237 |
skin | malignant_melanoma | Substitution - Missense |
c.915C>A; p.G305G; 16:766078-766078 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - coding silent |
c.199C>T; p.L67F; 16:764042-764042 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1193T>C; p.L398S; 16:766453-766453 |
liver | carcinoma | Substitution - Missense |
c.1144G>A; p.E382K; 16:766404-766404 |
skin | malignant_melanoma | Substitution - Missense |
c.1234C>T; p.P412S; 16:766647-766647 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1193T>C; p.L398S; 16:766453-766453 |
liver | carcinoma | Substitution - Missense |
c.1234C>G; p.P412A; 16:766647-766647 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1820G>A; p.G607E; 16:768660-768660 |
skin | malignant_melanoma | Substitution - Missense |
c.1889C>T; p.A630V; 16:768729-768729 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.961T>C; p.W321R; 16:766124-766124 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1384C>A; p.P462T; 16:766797-766797 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1585G>T; p.A529S; 16:767435-767435 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1142C>T; p.P381L; 16:766402-766402 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1570G>A; p.V524M; 16:767420-767420 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1593C>T; p.F531F; 16:767443-767443 |
skin | malignant_melanoma | Substitution - coding silent |
c.473A>T; p.E158V; 16:764999-764999 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.336C>T; p.P112P; 16:764682-764682 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1284G>T; p.K428N; 16:766697-766697 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.215C>T; p.A72V; 16:764058-764058 |
breast | carcinoma | Substitution - Missense |
c.215C>T; p.A72V; 16:764058-764058 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1772C>A; p.P591H; 16:768530-768530 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.874C>T; p.R292W; 16:765769-765769 |
ovary | carcinoma; adenocarcinoma | Substitution - Missense |
c.858G>A; p.R286R; 16:765753-765753 |
skin | malignant_melanoma | Substitution - coding silent |
c.1315G>T; p.D439Y; 16:766728-766728 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.324C>T; p.L108L; 16:764670-764670 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.706C>A; p.P236T; 16:765528-765528 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.739G>A; p.A247T; 16:765561-765561 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1495G>A; p.E499K; 16:766982-766982 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1495G>A; p.E499K; 16:766982-766982 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |