| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 3198 |
Name | HOXA1 |
Synonymous | homeobox A1;HOXA1;homeobox A1 |
Definition | HOX A1 homeodomain protein|Hox 1.6-like protein|homeo box A1|homeobox 1F|homeobox protein Hox-1F|homeobox protein Hox-A1|lab-like protein |
Position | 7p15.3 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.258G>T; p.L86L; 7:27095655-27095655 |
autonomic_ganglia | neuroblastoma | Substitution - coding silent |
c.838C>T; p.R280C; 7:27094610-27094610 |
breast | carcinoma | Substitution - Missense |
c.582C>T; p.P194P; 7:27095331-27095331 |
breast | carcinoma | Substitution - coding silent |
c.216_218delTCG; p.R73delR; 7:27095695-27095697 |
breast | carcinoma | Deletion - In frame |
c.583G>A; p.A195T; 7:27095330-27095330 |
breast | carcinoma | Substitution - Missense |
c.200A>C; p.H67P; 7:27095713-27095713 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.284G>A; p.C95Y; 7:27095629-27095629 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.580C>T; p.P194S; 7:27095333-27095333 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.773G>A; p.R258H; 7:27094675-27094675 |
central_nervous_system; temporoparietal | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.692C>T; p.A231V; 7:27094756-27094756 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.221A>G; p.H74R; 7:27095692-27095692 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.947C>A; p.S316Y; 7:27094501-27094501 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.697C>T; p.R233C; 7:27094751-27094751 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.154C>T; p.R52C; 7:27095759-27095759 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.180G>T; p.Q60H; 7:27095733-27095733 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.854A>T; p.K285M; 7:27094594-27094594 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.521C>T; p.A174V; 7:27095392-27095392 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.773G>A; p.R258H; 7:27094675-27094675 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.207_215delCCACCACCA; p.H70_H72delHHH; 7:27095698-27095706 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_T_cell_leukaemia | Deletion - In frame |
c.790G>T; p.A264S; 7:27094658-27094658 |
kidney | other; neoplasm | Substitution - Missense |
c.733G>A; p.E245K; 7:27094715-27094715 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.713C>A; p.T238N; 7:27094735-27094735 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.877T>C; p.L293L; 7:27094571-27094571 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.412C>T; p.P138S; 7:27095501-27095501 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.226delC; p.Q76fs*38; 7:27095687-27095687 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.215_216insCCA; p.H72_R73insH; 7:27095697-27095698 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - In frame |
c.215_216insCCA; p.H72_R73insH; 7:27095697-27095698 |
large_intestine | carcinoma; adenocarcinoma | Insertion - In frame |
c.194A>C; p.H65P; 7:27095719-27095719 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.822G>A; p.K274K; 7:27094626-27094626 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.334G>A; p.A112T; 7:27095579-27095579 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.281G>T; p.S94I; 7:27095632-27095632 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.950C>T; p.S317L; 7:27094498-27094498 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.333C>T; p.Y111Y; 7:27095580-27095580 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.738G>A; p.K246K; 7:27094710-27094710 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.922G>A; p.E308K; 7:27094526-27094526 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.216_218delTCG; p.R73delR; 7:27095695-27095697 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - In frame |
c.335C>T; p.A112V; 7:27095578-27095578 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.87_88insA; p.S30fs*4; 7:27095825-27095826 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.175delG; p.V59fs*55; 7:27095738-27095738 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.213_215delCCA; p.H72delH; 7:27095698-27095700 |
large_intestine | carcinoma; adenocarcinoma | Deletion - In frame |
c.652G>T; p.G218W; 7:27095261-27095261 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.652G>T; p.G218W; 7:27095261-27095261 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.697C>T; p.R233C; 7:27094751-27094751 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.397G>A; p.G133R; 7:27095516-27095516 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.121G>A; p.A41T; 7:27095792-27095792 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.553G>A; p.A185T; 7:27095360-27095360 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.207_215delCCACCACCA; p.H70_H72delHHH; 7:27095698-27095706 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - In frame |
c.773G>A; p.R258H; 7:27094675-27094675 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.913G>A; p.E305K; 7:27094535-27094535 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.859C>T; p.R287C; 7:27094589-27094589 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.494G>C; p.G165A; 7:27095419-27095419 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.797T>A; p.L266Q; 7:27094651-27094651 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.377G>T; p.C126F; 7:27095536-27095536 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.693G>A; p.A231A; 7:27094755-27094755 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.205C>A; p.H69N; 7:27095708-27095708 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.644C>A; p.P215H; 7:27095269-27095269 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.514G>T; p.A172S; 7:27095399-27095399 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.652G>T; p.G218W; 7:27095261-27095261 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.356T>A; p.V119E; 7:27095557-27095557 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.989C>G; p.T330S; 7:27094459-27094459 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.146G>T; p.G49V; 7:27095767-27095767 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.513G>T; p.L171L; 7:27095400-27095400 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.123G>T; p.A41A; 7:27095790-27095790 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.766C>T; p.R256C; 7:27094682-27094682 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.932C>A; p.S311*; 7:27094516-27094516 |
lung | carcinoma; small_cell_carcinoma | Substitution - Nonsense |
c.962C>A; p.P321H; 7:27094486-27094486 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.186T>C; p.G62G; 7:27095727-27095727 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.575G>A; p.R192H; 7:27095338-27095338 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.531_533delTAA; p.N178delN; 7:27095380-27095382 |
oesophagus | carcinoma; adenocarcinoma | Deletion - In frame |
c.505C>T; p.Q169*; 7:27095408-27095408 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.945C>T; p.S315S; 7:27094503-27094503 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.398G>A; p.G133E; 7:27095515-27095515 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.47G>C; p.S16T; 7:27095866-27095866 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.555C>A; p.A185A; 7:27095358-27095358 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.431A>T; p.H144L; 7:27095482-27095482 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.41T>C; p.I14T; 7:27095872-27095872 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.41T>C; p.I14T; 7:27095872-27095872 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.252G>T; p.G84G; 7:27095661-27095661 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.59C>T; p.S20L; 7:27095854-27095854 |
pancreas | carcinoma | Substitution - Missense |
c.859C>T; p.R287C; 7:27094589-27094589 |
peritoneum; appendix | other; pseudomyxoma_peritonei | Substitution - Missense |
c.909C>T; p.N303N; 7:27094539-27094539 |
prostate | carcinoma | Substitution - coding silent |
c.583G>A; p.A195T; 7:27095330-27095330 |
prostate | carcinoma | Substitution - Missense |
c.252G>A; p.G84G; 7:27095661-27095661 |
skin | malignant_melanoma | Substitution - coding silent |
c.829T>C; p.F277L; 7:27094619-27094619 |
skin | malignant_melanoma | Substitution - Missense |
c.260G>A; p.G87E; 7:27095653-27095653 |
skin | malignant_melanoma | Substitution - Missense |
c.4G>A; p.D2N; 7:27095909-27095909 |
skin | malignant_melanoma | Substitution - Missense |
c.786C>T; p.I262I; 7:27094662-27094662 |
skin | malignant_melanoma | Substitution - coding silent |
c.671G>A; p.G224D; 7:27094777-27094777 |
skin | malignant_melanoma | Substitution - Missense |
c.27C>T; p.F9F; 7:27095886-27095886 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.728A>T; p.E243V; 7:27094720-27094720 |
skin | malignant_melanoma | Substitution - Missense |
c.112C>T; p.Q38*; 7:27095801-27095801 |
skin | malignant_melanoma | Substitution - Nonsense |
c.981C>T; p.T327T; 7:27094467-27094467 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.840C>T; p.R280R; 7:27094608-27094608 |
skin | malignant_melanoma | Substitution - coding silent |
c.654G>A; p.G218G; 7:27094794-27094794 |
skin | malignant_melanoma | Substitution - coding silent |
c.587C>T; p.S196L; 7:27095326-27095326 |
skin | malignant_melanoma | Substitution - Missense |
c.165G>A; p.V55V; 7:27095748-27095748 |
skin | malignant_melanoma | Substitution - coding silent |
c.91G>A; p.D31N; 7:27095822-27095822 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.122C>T; p.A41V; 7:27095791-27095791 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.520G>T; p.A174S; 7:27095393-27095393 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.378C>T; p.C126C; 7:27095535-27095535 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.697C>T; p.R233C; 7:27094751-27094751 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.697C>T; p.R233C; 7:27094751-27094751 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.146G>A; p.G49D; 7:27095767-27095767 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.769G>A; p.A257T; 7:27094679-27094679 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.218G>A; p.R73H; 7:27095695-27095695 |
thyroid | other; neoplasm | Substitution - Missense |
c.638A>G; p.N213S; 7:27095275-27095275 |
thyroid | carcinoma | Substitution - Missense |
c.213C>T; p.H71H; 7:27095700-27095700 |
thyroid | other; neoplasm | Substitution - coding silent |
c.851A>G; p.Q284R; 7:27094597-27094597 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.216_218delTCG; p.R73delR; 7:27095695-27095697 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Deletion - In frame |
c.216_218delTCG; p.R73delR; 7:27095695-27095697 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Deletion - In frame |
c.216_218delTCG; p.R73delR; 7:27095695-27095697 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Deletion - In frame |
c.216_218delTCG; p.R73delR; 7:27095695-27095697 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Deletion - In frame |
c.126C>T; p.V42V; 7:27095787-27095787 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |