| Gene ID | 56892 |
| Symbol | C8orf4 |
| Synonymous | TC-1|TC1 |
| Full name | chromosome 8 open reading frame 4 |
| Gene description | human thyroid cancer 1|thyroid cancer protein 1|uncharacterized protein C8orf4 |
| Cytoband | 8p11.2 |
| Gene type | protein-coding |
| Synonymous | MIM:607702; HGNC:HGNC:1357; Ensembl:ENSG00000176907; HPRD:09650; Vega:OTTHUMG00000164045 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.167G>A; p.G56E; 8:40153699-40153699 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.295C>T; p.R99W; 8:40153827-40153827 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.66C>T; p.I22I; 8:40153598-40153598 |
skin | malignant_melanoma | Substitution - coding silent |
c.66C>T; p.I22I; 8:40153598-40153598 |
skin | malignant_melanoma | Substitution - coding silent |
c.105C>T; p.A35A; 8:40153637-40153637 |
breast | carcinoma | Substitution - coding silent |
c.62C>T; p.S21F; 8:40153594-40153594 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.183G>C; p.E61D; 8:40153715-40153715 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.152T>C; p.L51P; 8:40153684-40153684 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.44C>T; p.S15L; 8:40153576-40153576 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.261G>A; p.R87R; 8:40153793-40153793 |
liver | carcinoma | Substitution - coding silent |
c.137A>G; p.E46G; 8:40153669-40153669 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.121G>A; p.E41K; 8:40153653-40153653 |
skin | malignant_melanoma | Substitution - Missense |
c.164C>T; p.S55F; 8:40153696-40153696 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.50G>A; p.R17Q; 8:40153582-40153582 |
skin | malignant_melanoma | Substitution - Missense |
c.294G>A; p.L98L; 8:40153826-40153826 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.259A>C; p.R87R; 8:40153791-40153791 |
liver | carcinoma | Substitution - coding silent |
c.316C>T; p.H106Y; 8:40153848-40153848 |
skin | malignant_melanoma | Substitution - Missense |
c.67C>T; p.H23Y; 8:40153599-40153599 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.226G>A; p.E76K; 8:40153758-40153758 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.280C>T; p.Q94*; 8:40153812-40153812 |
skin | malignant_melanoma | Substitution - Nonsense |
c.14G>A; p.R5Q; 8:40153546-40153546 |
skin | malignant_melanoma | Substitution - Missense |
c.14G>A; p.R5Q; 8:40153546-40153546 |
skin | malignant_melanoma | Substitution - Missense |
c.234G>A; p.T78T; 8:40153766-40153766 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.234G>A; p.T78T; 8:40153766-40153766 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.94C>T; p.R32C; 8:40153626-40153626 |
skin | malignant_melanoma | Substitution - Missense |
c.233C>T; p.T78M; 8:40153765-40153765 |
skin | malignant_melanoma | Substitution - Missense |