| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 894 | ||
Name | CCND2 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.557C>G; p.A186G; 12:4278905-4278905 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.599C>T; p.S200L; 12:4288869-4288869 |
liver | carcinoma | Substitution - Missense |
c.599C>T; p.S200L; 12:4288869-4288869 |
skin | malignant_melanoma | Substitution - Missense |
c.599C>T; p.S200L; 12:4288869-4288869 |
skin | malignant_melanoma | Substitution - Missense |
c.599C>T; p.S200L; 12:4288869-4288869 |
liver | carcinoma | Substitution - Missense |
c.318G>C; p.M106I; 12:4276127-4276127 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.803G>A; p.G268E; 12:4299942-4299942 |
skin | malignant_melanoma | Substitution - Missense |
c.803G>A; p.G268E; 12:4299942-4299942 |
skin | malignant_melanoma | Substitution - Missense |
c.763C>T; p.L255F; 12:4299902-4299902 |
skin | malignant_melanoma | Substitution - Missense |
c.784C>A; p.R262S; 12:4299923-4299923 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.120G>T; p.Q40H; 12:4274160-4274160 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.784C>T; p.R262C; 12:4299923-4299923 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.783C>G; p.Y261*; 12:4299922-4299922 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.576T>C; p.F192F; 12:4288846-4288846 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.411+1G>T; p.?; 12:4276221-4276221 |
endometrium | carcinoma; endometrioid_carcinoma | Unknown |
c.600G>A; p.S200S; 12:4288870-4288870 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.600G>A; p.S200S; 12:4288870-4288870 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.722A>T; p.D241V; 12:4299861-4299861 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.600G>A; p.S200S; 12:4288870-4288870 |
pancreas | carcinoma | Substitution - coding silent |
c.208C>A; p.Q70K; 12:4276017-4276017 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.299T>G; p.L100R; 12:4276108-4276108 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.299T>G; p.L100R; 12:4276108-4276108 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.299T>G; p.L100R; 12:4276108-4276108 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.494G>A; p.R165H; 12:4278842-4278842 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.778C>T; p.Q260*; 12:4299917-4299917 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Nonsense |
c.747G>T; p.Q249H; 12:4299886-4299886 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.228C>T; p.V76V; 12:4276037-4276037 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.607G>A; p.A203T; 12:4288877-4288877 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.606C>T; p.I202I; 12:4288876-4288876 |
skin | malignant_melanoma | Substitution - coding silent |
c.801C>T; p.D267D; 12:4299940-4299940 |
pancreas | carcinoma | Substitution - coding silent |
c.868T>C; p.*290R; 12:4300007-4300007 |
large_intestine; colon | carcinoma; adenocarcinoma | Nonstop extension |
c.412-1G>A; p.?; 12:4278759-4278759 |
skin | malignant_melanoma | Unknown |
c.556G>A; p.A186T; 12:4278904-4278904 |
breast | carcinoma | Substitution - Missense |
c.216C>A; p.C72*; 12:4276025-4276025 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.572-1G>T; p.?; 12:4288841-4288841 |
endometrium | carcinoma; endometrioid_carcinoma | Unknown |
c.534C>G; p.R178R; 12:4278882-4278882 |
prostate | carcinoma | Substitution - coding silent |
c.520C>T; p.L174L; 12:4278868-4278868 |
breast | carcinoma | Substitution - coding silent |
c.789G>A; p.Q263Q; 12:4299928-4299928 |
skin | malignant_melanoma | Substitution - coding silent |
c.569C>T; p.T190I; 12:4278917-4278917 |
pancreas | carcinoma | Substitution - Missense |
c.838A>G; p.T280A; 12:4299977-4299977 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.437A>G; p.K146R; 12:4278785-4278785 |
central_nervous_system; occipital_lobe | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.276G>A; p.P92P; 12:4276085-4276085 |
skin | malignant_melanoma | Substitution - coding silent |
c.393C>G; p.I131M; 12:4276202-4276202 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.850G>A; p.V284M; 12:4299989-4299989 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.793C>T; p.Q265*; 12:4299932-4299932 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Nonsense |
c.193G>C; p.E65Q; 12:4274233-4274233 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.137G>A; p.C46Y; 12:4274177-4274177 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.817G>A; p.D273N; 12:4299956-4299956 |
skin | malignant_melanoma | Substitution - Missense |
c.861C>T; p.I287I; 12:4300000-4300000 |
skin | malignant_melanoma | Substitution - coding silent |
c.802G>C; p.G268R; 12:4299941-4299941 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.371G>A; p.C124Y; 12:4276180-4276180 |
skin | malignant_melanoma | Substitution - Missense |
c.742G>A; p.E248K; 12:4299881-4299881 |
skin | malignant_melanoma | Substitution - Missense |
c.584C>G; p.A195G; 12:4288854-4288854 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.853C>T; p.R285W; 12:4299992-4299992 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.281C>T; p.P94L; 12:4276090-4276090 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.802G>T; p.G268*; 12:4299941-4299941 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.842C>T; p.P281L; 12:4299981-4299981 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.524C>T; p.S175F; 12:4278872-4278872 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.524C>T; p.S175F; 12:4278872-4278872 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.70G>A; p.D24N; 12:4274110-4274110 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.493C>T; p.R165C; 12:4278841-4278841 |
breast | carcinoma | Substitution - Missense |
c.453G>C; p.L151L; 12:4278801-4278801 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.132C>T; p.F44F; 12:4274172-4274172 |
skin | malignant_melanoma | Substitution - coding silent |
c.132C>T; p.F44F; 12:4274172-4274172 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.674G>C; p.C225S; 12:4288944-4288944 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.559C>A; p.L187M; 12:4278907-4278907 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.152T>G; p.I51S; 12:4274192-4274192 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.785G>T; p.R262L; 12:4299924-4299924 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.418G>A; p.E140K; 12:4278766-4278766 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.584C>T; p.A195V; 12:4288854-4288854 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.633C>T; p.I211I; 12:4288903-4288903 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.65G>A; p.R22Q; 12:4274105-4274105 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.472G>T; p.D158Y; 12:4278820-4278820 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.855G>A; p.R285R; 12:4299994-4299994 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.585C>T; p.A195A; 12:4288855-4288855 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.839C>A; p.T280N; 12:4299978-4299978 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.114T>C; p.L38L; 12:4274154-4274154 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.841C>T; p.P281S; 12:4299980-4299980 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.393C>A; p.I131I; 12:4276202-4276202 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.593C>G; p.P198R; 12:4288863-4288863 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.393C>A; p.I131I; 12:4276202-4276202 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.842C>G; p.P281R; 12:4299981-4299981 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.329C>G; p.S110C; 12:4276138-4276138 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.244A>C; p.N82H; 12:4276053-4276053 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.279T>G; p.T93T; 12:4276088-4276088 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |