| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 91862 | ||
Name | MARVELD3 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1123G>A; p.V375M; 16:71640917-71640917 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.481G>A; p.E161K; 16:71629380-71629380 |
skin | malignant_melanoma | Substitution - Missense |
c.1226C>G; p.T409S; 16:71641020-71641020 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1186G>A; p.G396R; 16:71640980-71640980 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.481G>A; p.E161K; 16:71629380-71629380 |
skin | malignant_melanoma | Substitution - Missense |
c.1126G>A; p.V376M; 16:71640920-71640920 |
skin | malignant_melanoma | Substitution - Missense |
c.1115G>A; p.G372D; 16:71640909-71640909 |
skin | malignant_melanoma | Substitution - Missense |
c.798G>A; p.L266L; 16:71640592-71640592 |
skin | malignant_melanoma | Substitution - coding silent |
c.1160G>A; p.R387H; 16:71640954-71640954 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.966C>G; p.L322L; 16:71640760-71640760 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.541G>C; p.E181Q; 16:71629440-71629440 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.172G>A; p.D58N; 16:71626401-71626401 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.887C>T; p.S296L; 16:71640681-71640681 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.887C>T; p.S296L; 16:71640681-71640681 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.497C>T; p.S166L; 16:71629396-71629396 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.324A>C; p.E108D; 16:71626553-71626553 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.514C>T; p.R172*; 16:71629413-71629413 |
skin | malignant_melanoma | Substitution - Nonsense |
c.514C>T; p.R172*; 16:71629413-71629413 |
oesophagus | carcinoma | Substitution - Nonsense |
c.1117G>A; p.A373T; 16:71640911-71640911 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.1206G>A; p.P402P; 16:71641000-71641000 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.621C>A; p.V207V; 16:71640415-71640415 |
thyroid | other; neoplasm | Substitution - coding silent |
c.974C>A; p.A325D; 16:71640768-71640768 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1010G>A; p.R337K; 16:71640804-71640804 |
skin | malignant_melanoma | Substitution - Missense |
c.674G>A; p.G225E; 16:71640468-71640468 |
skin | malignant_melanoma | Substitution - Missense |
c.804C>T; p.Y268Y; 16:71640598-71640598 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.874C>T; p.R292*; 16:71640668-71640668 |
pancreas | carcinoma | Substitution - Nonsense |
c.874C>T; p.R292*; 16:71640668-71640668 |
pancreas | carcinoma | Substitution - Nonsense |
c.700G>A; p.G234S; 16:71640494-71640494 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1165A>G; p.K389E; 16:71640959-71640959 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1059_1065delGGCAGGC; p.A354fs*13; 16:71640853-71640859 |
breast | carcinoma | Deletion - Frameshift |
c.82G>A; p.G28S; 16:71626311-71626311 |
NS | malignant_melanoma | Substitution - Missense |
c.1113C>T; p.Y371Y; 16:71640907-71640907 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1139G>A; p.R380H; 16:71640933-71640933 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.792G>A; p.S264S; 16:71640586-71640586 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1044G>A; p.W348*; 16:71640838-71640838 |
skin | malignant_melanoma | Substitution - Nonsense |
c.476C>G; p.P159R; 16:71629375-71629375 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.672C>T; p.A224A; 16:71640466-71640466 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.272G>A; p.R91Q; 16:71626501-71626501 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.479C>T; p.S160L; 16:71629378-71629378 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1067C>T; p.T356I; 16:71640861-71640861 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.737G>A; p.G246D; 16:71640531-71640531 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.796C>A; p.L266M; 16:71640590-71640590 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.550G>A; p.G184R; 16:71629449-71629449 |
skin | malignant_melanoma | Substitution - Missense |
c.1029C>T; p.R343R; 16:71640823-71640823 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.637C>A; p.L213I; 16:71640431-71640431 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.564C>T; p.C188C; 16:71629463-71629463 |
breast | carcinoma | Substitution - coding silent |
c.792G>T; p.S264S; 16:71640586-71640586 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1002C>T; p.C334C; 16:71640796-71640796 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - coding silent |
c.780G>A; p.T260T; 16:71640574-71640574 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.757C>T; p.R253W; 16:71640551-71640551 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1175G>A; p.R392Q; 16:71640969-71640969 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.875G>A; p.R292Q; 16:71640669-71640669 |
skin | malignant_melanoma | Substitution - Missense |
c.875G>A; p.R292Q; 16:71640669-71640669 |
skin | malignant_melanoma | Substitution - Missense |
c.578A>G; p.Y193C; 16:71629477-71629477 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1054C>A; p.Q352K; 16:71640848-71640848 |
skin; ear | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.906G>A; p.T302T; 16:71640700-71640700 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.652G>A; p.A218T; 16:71640446-71640446 |
skin | malignant_melanoma | Substitution - Missense |
c.491T>A; p.L164Q; 16:71629390-71629390 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.878C>T; p.T293I; 16:71640672-71640672 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.275_276delAC; p.H94fs*9; 16:71626504-71626505 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - Frameshift |
c.500C>T; p.T167I; 16:71629399-71629399 |
skin; abdomen | malignant_melanoma | Substitution - Missense |
c.178G>A; p.E60K; 16:71626407-71626407 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.728C>T; p.P243L; 16:71640522-71640522 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.765_766GG>AA; p.D256N; 16:71640559-71640560 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.728C>T; p.P243L; 16:71640522-71640522 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.501C>T; p.T167T; 16:71629400-71629400 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.572G>A; p.C191Y; 16:71629471-71629471 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.514C>A; p.R172R; 16:71629413-71629413 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |