| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 8451 |
Name | CUL4A |
Synonymous | cullin 4A;CUL4A;cullin 4A |
Definition | CUL-4A|cullin-4A |
Position | 13q34 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.846G>A; p.K282K; 13:113243078-113243078 |
breast | carcinoma | Substitution - coding silent |
c.112T>G; p.C38G; 13:113228019-113228019 |
breast | carcinoma; ductal_carcinoma | Substitution - Missense |
c.1781A>G; p.Y594C; 13:113260656-113260656 |
breast | carcinoma | Substitution - Missense |
c.1005G>C; p.K335N; 13:113244486-113244486 |
breast | carcinoma | Substitution - Missense |
c.1591C>T; p.L531L; 13:113254985-113254985 |
breast | carcinoma; lobular_carcinoma | Substitution - coding silent |
c.1145-1G>A; p.?; 13:113245151-113245151 |
breast | carcinoma | Unknown |
c.561T>C; p.I187I; 13:113236835-113236835 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.376-2A>C; p.?; 13:113233895-113233895 |
central_nervous_system; medulla | primitive_neuroectodermal_tumour-medulloblastoma; classic | Unknown |
c.1717C>G; p.Q573E; 13:113255111-113255111 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.790G>C; p.D264H; 13:113243022-113243022 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1550C>T; p.T517M; 13:113254790-113254790 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.604A>G; p.I202V; 13:113236878-113236878 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.903A>G; p.R301R; 13:113243135-113243135 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.724G>A; p.E242K; 13:113239540-113239540 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.995C>T; p.T332M; 13:113244476-113244476 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.385G>T; p.D129Y; 13:113233906-113233906 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.579G>T; p.Q193H; 13:113236853-113236853 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.967G>T; p.E323*; 13:113244448-113244448 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.324C>T; p.A108A; 13:113233288-113233288 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1511A>C; p.E504A; 13:113254751-113254751 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.651G>A; p.P217P; 13:113239467-113239467 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1834C>G; p.H612D; 13:113260709-113260709 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.123C>T; p.D41D; 13:113228030-113228030 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1440G>A; p.A480A; 13:113253183-113253183 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.520G>A; p.V174I; 13:113235117-113235117 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.325G>A; p.V109M; 13:113233289-113233289 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.774C>T; p.D258D; 13:113243006-113243006 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1971C>T; p.Y657Y; 13:113263573-113263573 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.704C>T; p.A235V; 13:113239520-113239520 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1367C>T; p.A456V; 13:113253110-113253110 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.753C>T; p.I251I; 13:113242985-113242985 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1631A>G; p.K544R; 13:113255025-113255025 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1694T>G; p.F565C; 13:113255088-113255088 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1469A>G; p.Q490R; 13:113254709-113254709 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1093_1094delAA; p.S366fs*6; 13:113245008-113245009 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1470G>T; p.Q490H; 13:113254710-113254710 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.748G>A; p.A250T; 13:113242980-113242980 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1726G>A; p.E576K; 13:113255120-113255120 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1373A>G; p.Y458C; 13:113253116-113253116 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.693C>T; p.G231G; 13:113239509-113239509 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1468C>T; p.Q490*; 13:113254708-113254708 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1107C>T; p.V369V; 13:113245022-113245022 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1140G>A; p.K380K; 13:113245055-113245055 |
liver | carcinoma | Substitution - coding silent |
c.1108G>A; p.D370N; 13:113245023-113245023 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1074delA; p.R360fs*62; 13:113244989-113244989 |
liver | carcinoma | Deletion - Frameshift |
c.1402C>T; p.Q468*; 13:113253145-113253145 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.872A>G; p.K291R; 13:113243104-113243104 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.658G>T; p.A220S; 13:113239474-113239474 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.906C>T; p.P302P; 13:113243138-113243138 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.823G>A; p.V275M; 13:113243055-113243055 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1446_1447insT; p.K483fs*1; 13:113253189-113253190 |
lung | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1029C>G; p.I343M; 13:113244510-113244510 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.300C>T; p.I100I; 13:113233264-113233264 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.139-1G>C; p.?; 13:113229445-113229445 |
lung | carcinoma; adenocarcinoma | Unknown |
c.1452+1G>C; p.?; 13:113253196-113253196 |
lung | carcinoma; adenocarcinoma | Unknown |
c.169G>A; p.D57N; 13:113229476-113229476 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.297G>T; p.L99L; 13:113233261-113233261 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.955G>A; p.A319T; 13:113244436-113244436 |
NS | malignant_melanoma | Substitution - Missense |
c.1422A>G; p.G474G; 13:113253165-113253165 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1563T>C; p.D521D; 13:113254957-113254957 |
ovary | other; neoplasm | Substitution - coding silent |
c.123C>T; p.D41D; 13:113228030-113228030 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1595C>T; p.A532V; 13:113254989-113254989 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1590C>T; p.S530S; 13:113254984-113254984 |
skin | malignant_melanoma | Substitution - coding silent |
c.1590C>T; p.S530S; 13:113254984-113254984 |
skin | malignant_melanoma | Substitution - coding silent |
c.194C>T; p.S65F; 13:113229501-113229501 |
skin | malignant_melanoma | Substitution - Missense |
c.194C>T; p.S65F; 13:113229501-113229501 |
skin | malignant_melanoma | Substitution - Missense |
c.194C>T; p.S65F; 13:113229501-113229501 |
skin | malignant_melanoma | Substitution - Missense |
c.1084C>T; p.L362F; 13:113244999-113244999 |
skin | malignant_melanoma | Substitution - Missense |
c.937G>A; p.V313M; 13:113244418-113244418 |
skin | malignant_melanoma | Substitution - Missense |
c.1321G>A; p.V441M; 13:113246046-113246046 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.805A>C; p.K269Q; 13:113243037-113243037 |
skin | malignant_melanoma | Substitution - Missense |
c.1398A>G; p.K466K; 13:113253141-113253141 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1083C>T; p.L361L; 13:113244998-113244998 |
skin | malignant_melanoma | Substitution - coding silent |
c.1561G>A; p.D521N; 13:113254955-113254955 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1457A>G; p.K486R; 13:113254697-113254697 |
skin | malignant_melanoma | Substitution - Missense |
c.1212C>T; p.I404I; 13:113245219-113245219 |
skin | malignant_melanoma | Substitution - coding silent |
c.1219C>T; p.H407Y; 13:113245226-113245226 |
skin | malignant_melanoma | Substitution - Missense |
c.1030C>T; p.H344Y; 13:113244511-113244511 |
skin; scalp | malignant_melanoma | Substitution - Missense |
c.1558+2T>C; p.?; 13:113254800-113254800 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.1256G>A; p.G419D; 13:113245981-113245981 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1311G>A; p.T437T; 13:113246036-113246036 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.755T>C; p.V252A; 13:113242987-113242987 |
stomach | adenocarcinoma | Substitution - Missense |
c.340T>C; p.L114L; 13:113233304-113233304 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1100C>T; p.A367V; 13:113245015-113245015 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.622G>A; p.D208N; 13:113239438-113239438 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1258C>T; p.P420S; 13:113245983-113245983 |
thyroid | other; neoplasm | Substitution - Missense |
c.774C>T; p.D258D; 13:113243006-113243006 |
thyroid | other; neoplasm | Substitution - coding silent |
c.705G>T; p.A235A; 13:113239521-113239521 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1815G>C; p.K605N; 13:113260690-113260690 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1245G>T; p.Q415H; 13:113245970-113245970 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1919T>A; p.I640K; 13:113263521-113263521 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1919T>A; p.I640K; 13:113263521-113263521 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.319G>A; p.E107K; 13:113233283-113233283 |
urinary_tract; bladder | carcinoma | Substitution - Missense |