General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 9486 |
Name | CHST10 |
Synonymous | carbohydrate sulfotransferase 10;CHST10;carbohydrate sulfotransferase 10 |
Definition | HNK-1 sulfotransferase|huHNK-1ST |
Position | 2q11.2 |
Gene Type | protein-coding |
Mutation summary: | Mutations in domains Mutational pattern in 17 major cancer types LoF vs missense mutations All the copy number variations from COSMIC database V72 All the mutations from COSMIC database V72 |
Mutation summary in protein domains | Top |
The non-synonymous (top) and synonymous (bottom) mutational percentage for various cancers | Top |
Loss of Function mutations compare to missense mutations | Top |
The ratio of the loss-of-function mutations over missense mutations is 0.13. |
The copy number variations for various cancers | Top |
The copy number variations in 17 major cancer types: 1; Breast, 2; Central nervous system, 3; Cervix, 4; Endometrium, 5; Haematopoietic and lymphoid_tissue, 6; Kidney, 7; Large intestine, 8; Liver, 9; Lung, 10; Not specific, 11; Ovary, 12; Pancreas, 13; Prostate, 14; Skin, 15; Stomach, 16; Thyroid, 17; Urinary tract |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) |
Site |
Histology |
Mutation Type |
---|---|---|---|
c.961G>T; p.E321*; 2:100393355-100393355 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.27C>T; p.A9A; 2:100406649-100406649 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.498G>A; p.R166R; 2:100395544-100395544 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.498G>A; p.R166R; 2:100395544-100395544 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.235C>A; p.L79M; 2:100398100-100398100 |
liver | carcinoma | Substitution - Missense |
c.235C>A; p.L79M; 2:100398100-100398100 |
liver | carcinoma | Substitution - Missense |
c.535T>A; p.L179M; 2:100393781-100393781 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.720C>T; p.F240F; 2:100393596-100393596 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.720C>T; p.F240F; 2:100393596-100393596 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.720C>T; p.F240F; 2:100393596-100393596 |
skin | malignant_melanoma | Substitution - coding silent |
c.251G>A; p.R84H; 2:100398084-100398084 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.686G>A; p.R229Q; 2:100393630-100393630 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.561T>C; p.I187I; 2:100393755-100393755 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.317C>T; p.S106F; 2:100398018-100398018 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.107G>A; p.S36N; 2:100402649-100402649 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.107G>A; p.S36N; 2:100402649-100402649 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.276C>A; p.C92*; 2:100398059-100398059 |
ovary | carcinoma; serous_carcinoma | Substitution - Nonsense |
c.276C>A; p.C92*; 2:100398059-100398059 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.418G>T; p.V140F; 2:100397917-100397917 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.623G>A; p.R208Q; 2:100393693-100393693 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.733G>A; p.G245S; 2:100393583-100393583 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.877A>G; p.I293V; 2:100393439-100393439 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.767T>G; p.F256C; 2:100393549-100393549 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.300C>A; p.L100L; 2:100398035-100398035 |
skin | malignant_melanoma | Substitution - coding silent |
c.742A>T; p.N248Y; 2:100393574-100393574 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.719T>C; p.F240S; 2:100393597-100393597 |
skin | malignant_melanoma | Substitution - Missense |
c.300C>A; p.L100L; 2:100398035-100398035 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1018G>A; p.E340K; 2:100393298-100393298 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.820G>T; p.E274*; 2:100393496-100393496 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Nonsense |
c.488G>A; p.G163D; 2:100395554-100395554 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.550A>G; p.K184E; 2:100393766-100393766 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - Missense |
c.890C>A; p.A297D; 2:100393426-100393426 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.497G>A; p.R166Q; 2:100395545-100395545 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.702delG; p.I235fs*18; 2:100393614-100393614 |
large_intestine; rectum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1041G>T; p.G347G; 2:100393275-100393275 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.453C>T; p.I151I; 2:100395589-100395589 |
skin | malignant_melanoma | Substitution - coding silent |
c.15G>A; p.W5*; 2:100406661-100406661 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.681G>T; p.R227S; 2:100393635-100393635 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.996C>A; p.I332I; 2:100393320-100393320 |
oesophagus | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.100+4C>T; p.?; 2:100406572-100406572 |
pancreas | carcinoma | Unknown |
c.759C>T; p.D253D; 2:100393557-100393557 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1048A>G; p.K350E; 2:100393268-100393268 |
skin | malignant_melanoma | Substitution - Missense |
c.47T>C; p.F16S; 2:100406629-100406629 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.276C>T; p.C92C; 2:100398059-100398059 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.584_585delTT; p.L195fs*5; 2:100393731-100393732 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - Frameshift |
c.70T>C; p.F24L; 2:100406606-100406606 |
skin | malignant_melanoma | Substitution - Missense |
c.184G>C; p.E62Q; 2:100402572-100402572 |
skin | malignant_melanoma | Substitution - Missense |
c.740C>T; p.P247L; 2:100393576-100393576 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.225C>T; p.L75L; 2:100398110-100398110 |
skin | malignant_melanoma | Substitution - coding silent |
c.389G>T; p.G130V; 2:100397946-100397946 |
liver | carcinoma | Substitution - Missense |
c.794C>T; p.T265M; 2:100393522-100393522 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.724C>T; p.R242C; 2:100393592-100393592 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.736G>A; p.D246N; 2:100393580-100393580 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.844C>T; p.H282Y; 2:100393472-100393472 |
thyroid | carcinoma | Substitution - Missense |
c.1A>G; p.M1V; 2:100406675-100406675 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.721G>A; p.V241M; 2:100393595-100393595 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.961G>C; p.E321Q; 2:100393355-100393355 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.568G>T; p.D190Y; 2:100393748-100393748 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.439T>A; p.S147T; 2:100395603-100395603 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1017C>T; p.F339F; 2:100393299-100393299 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1017C>T; p.F339F; 2:100393299-100393299 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.110C>T; p.A37V; 2:100402646-100402646 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.275G>T; p.C92F; 2:100398060-100398060 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.577G>A; p.E193K; 2:100393739-100393739 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.577G>A; p.E193K; 2:100393739-100393739 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.577G>A; p.E193K; 2:100393739-100393739 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.577G>A; p.E193K; 2:100393739-100393739 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.685C>T; p.R229W; 2:100393631-100393631 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.685C>T; p.R229W; 2:100393631-100393631 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.785A>T; p.H262L; 2:100393531-100393531 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.850G>A; p.E284K; 2:100393466-100393466 |
pancreas | carcinoma | Substitution - Missense |
c.850G>A; p.E284K; 2:100393466-100393466 |
pancreas | carcinoma | Substitution - Missense |
c.294G>A; p.K98K; 2:100398041-100398041 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.870C>T; p.A290A; 2:100393446-100393446 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.77C>T; p.T26M; 2:100406599-100406599 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.77C>T; p.T26M; 2:100406599-100406599 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.918G>A; p.P306P; 2:100393398-100393398 |
oesophagus | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.918G>A; p.P306P; 2:100393398-100393398 |
thyroid | carcinoma | Substitution - coding silent |
c.918G>A; p.P306P; 2:100393398-100393398 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1001G>A; p.R334H; 2:100393315-100393315 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.929C>T; p.P310L; 2:100393387-100393387 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.455C>T; p.P152L; 2:100395587-100395587 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.929C>T; p.P310L; 2:100393387-100393387 |
skin | malignant_melanoma | Substitution - Missense |
c.929C>T; p.P310L; 2:100393387-100393387 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.929C>T; p.P310L; 2:100393387-100393387 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1000C>T; p.R334C; 2:100393316-100393316 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.659G>A; p.G220D; 2:100393657-100393657 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.144G>A; p.P48P; 2:100402612-100402612 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.302C>T; p.S101L; 2:100398033-100398033 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.302C>T; p.S101L; 2:100398033-100398033 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |