| Gene ID | 978 |
| Symbol | CDA |
| Synonymous | CDD |
| Full name | cytidine deaminase |
| Gene description | cytidine aminohydrolase|cytosine nucleoside deaminase|small cytidine deaminase |
| Cytoband | 1p36.2-p35 |
| Gene type | protein-coding |
| Synonymous | MIM:123920; HGNC:HGNC:1712; Ensembl:ENSG00000158825; HPRD:11744; Vega:OTTHUMG00000002845 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.28C>G; p.L10V; 1:20589157-20589157 |
bone; pelvis | chondrosarcoma | Substitution - Missense |
c.182C>A; p.P61Q; 1:20604955-20604955 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.240G>T; p.K80N; 1:20605013-20605013 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.50A>T; p.Q17L; 1:20589179-20589179 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.140G>A; p.G47E; 1:20589269-20589269 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.435C>T; p.T145T; 1:20618562-20618562 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.435C>T; p.T145T; 1:20618562-20618562 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.413G>A; p.G138E; 1:20618540-20618540 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.413G>A; p.G138E; 1:20618540-20618540 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.202C>T; p.R68W; 1:20604975-20604975 |
skin; scalp | malignant_melanoma | Substitution - Missense |
c.325T>G; p.F109V; 1:20618452-20618452 |
breast | carcinoma | Substitution - Missense |
c.250G>A; p.A84T; 1:20605023-20605023 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.241G>T; p.D81Y; 1:20605014-20605014 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.79A>C; p.K27Q; 1:20589208-20589208 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.79A>C; p.K27Q; 1:20589208-20589208 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.79A>C; p.K27Q; 1:20589208-20589208 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.223G>A; p.V75I; 1:20604996-20604996 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.223G>A; p.V75I; 1:20604996-20604996 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.78G>T; p.K26N; 1:20589207-20589207 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.360G>A; p.P120P; 1:20618487-20618487 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.325-1G>C; p.?; 1:20618451-20618451 |
pancreas | carcinoma; acinar_carcinoma | Unknown |
c.262G>A; p.A88T; 1:20605035-20605035 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.262G>A; p.A88T; 1:20605035-20605035 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.353C>T; p.T118I; 1:20618480-20618480 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.233G>A; p.G78E; 1:20605006-20605006 |
skin | malignant_melanoma | Substitution - Missense |
c.426G>T; p.L142L; 1:20618553-20618553 |
prostate | carcinoma | Substitution - coding silent |
c.208G>A; p.A70T; 1:20604981-20604981 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.271A>G; p.M91V; 1:20613846-20613846 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.203G>T; p.R68L; 1:20604976-20604976 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.234G>A; p.G78G; 1:20605007-20605007 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.417T>C; p.P139P; 1:20618544-20618544 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.434delC; p.Q146fs?; 1:20618561-20618561 |
oesophagus; upper_third | carcinoma; squamous_cell_carcinoma | Deletion - Frameshift |
c.254T>C; p.I85T; 1:20605027-20605027 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.407C>T; p.S136F; 1:20618534-20618534 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.30G>A; p.L10L; 1:20589159-20589159 |
skin | malignant_melanoma | Substitution - coding silent |
c.348C>T; p.Y116Y; 1:20618475-20618475 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.137_138insG; p.R48fs*20; 1:20589266-20589267 |
liver | carcinoma | Insertion - Frameshift |
c.224T>C; p.V75A; 1:20604997-20604997 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.224T>C; p.V75A; 1:20604997-20604997 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.261C>T; p.I87I; 1:20605034-20605034 |
skin | malignant_melanoma | Substitution - coding silent |
c.52C>T; p.L18L; 1:20589181-20589181 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.261C>T; p.I87I; 1:20605034-20605034 |
skin | malignant_melanoma | Substitution - coding silent |
c.150C>T; p.F50F; 1:20589279-20589279 |
skin | malignant_melanoma | Substitution - coding silent |