| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 3276 | ||
Name | PRMT1 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.273C>T; p.I91I; 19:49682062-49682062 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.858G>T; p.T286T; 19:49686624-49686624 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.630G>A; p.E210E; 19:49684980-49684980 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.95C>G; p.S32C; 19:49680563-49680563 |
breast | carcinoma | Substitution - Missense |
c.948C>T; p.N316N; 19:49686714-49686714 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.975_977delCAC; p.T326delT; 19:49688176-49688178 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - In frame |
c.512G>A; p.R171Q; 19:49684782-49684782 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.448C>T; p.L150F; 19:49684034-49684034 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.858G>A; p.T286T; 19:49686624-49686624 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.213C>T; p.V71V; 19:49682002-49682002 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.182A>G; p.H61R; 19:49681971-49681971 |
pancreas | carcinoma; ductal_carcinoma | Substitution - Missense |
c.737C>G; p.P246R; 19:49686142-49686142 |
skin | malignant_melanoma | Substitution - Missense |
c.255C>T; p.A85A; 19:49682044-49682044 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.775G>T; p.A259S; 19:49686180-49686180 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1040G>C; p.R347P; 19:49688241-49688241 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.443C>G; p.S148C; 19:49684029-49684029 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.825C>T; p.T275T; 19:49686230-49686230 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.987G>C; p.L329L; 19:49688188-49688188 |
large_intestine; colon | adenoma | Substitution - coding silent |
c.567C>T; p.I189I; 19:49684837-49684837 |
skin | malignant_melanoma | Substitution - coding silent |
c.143G>A; p.R48H; 19:49681932-49681932 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.135C>T; p.D45D; 19:49681924-49681924 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.844G>A; p.E282K; 19:49686610-49686610 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.699C>G; p.I233M; 19:49686104-49686104 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.457G>A; p.V153M; 19:49684043-49684043 |
pancreas | carcinoma; acinar_carcinoma | Substitution - Missense |
c.19G>T; p.V7L; 19:49680487-49680487 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; follicular_lymphoma | Substitution - Missense |
c.402C>T; p.I134I; 19:49683988-49683988 |
skin | malignant_melanoma | Substitution - coding silent |
c.235T>A; p.C79S; 19:49682024-49682024 |
pancreas | carcinoma | Substitution - Missense |
c.289A>G; p.S97G; 19:49682208-49682208 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1026C>T; p.T342T; 19:49688227-49688227 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - coding silent |
c.1026C>T; p.T342T; 19:49688227-49688227 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.936C>T; p.G312G; 19:49686702-49686702 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.738G>A; p.P246P; 19:49686143-49686143 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.464A>G; p.Y155C; 19:49684050-49684050 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.243T>C; p.F81F; 19:49682032-49682032 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.490G>A; p.D164N; 19:49684760-49684760 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.873G>A; p.T291T; 19:49686639-49686639 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.873G>A; p.T291T; 19:49686639-49686639 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.944C>T; p.P315L; 19:49686710-49686710 |
skin | malignant_melanoma | Substitution - Missense |
c.988G>C; p.D330H; 19:49688189-49688189 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.450C>A; p.L150L; 19:49684036-49684036 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.189C>T; p.F63F; 19:49681978-49681978 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.913G>A; p.E305K; 19:49686679-49686679 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.903G>A; p.V301V; 19:49686669-49686669 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.737C>T; p.P246L; 19:49686142-49686142 |
skin | malignant_melanoma | Substitution - Missense |
c.450C>T; p.L150L; 19:49684036-49684036 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.693G>A; p.V231V; 19:49686098-49686098 |
breast | carcinoma | Substitution - coding silent |
c.949G>A; p.A317T; 19:49686715-49686715 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.647T>C; p.V216A; 19:49684997-49684997 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1042T>C; p.*348R; 19:49688243-49688243 |
stomach | carcinoma; adenocarcinoma | Nonstop extension |
c.850C>T; p.P284S; 19:49686616-49686616 |
skin | malignant_melanoma | Substitution - Missense |
c.1040G>A; p.R347H; 19:49688241-49688241 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1027G>A; p.D343N; 19:49688228-49688228 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.621C>T; p.A207A; 19:49684971-49684971 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - coding silent |
c.186C>T; p.L62L; 19:49681975-49681975 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.582C>T; p.N194N; 19:49684932-49684932 |
liver | carcinoma | Substitution - coding silent |
c.769G>A; p.V257M; 19:49686174-49686174 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.449T>C; p.L150P; 19:49684035-49684035 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.449T>C; p.L150P; 19:49684035-49684035 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.757C>T; p.R253W; 19:49686162-49686162 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.594C>T; p.F198F; 19:49684944-49684944 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |