| General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information | |
|---|---|
Gene ID | 51684 |
Name | SUFU |
Synonymous | PRO1280|SUFUH|SUFUXL;suppressor of fused homolog (Drosophila);SUFU;suppressor of fused homolog (Drosophila) |
Definition | suppressor of fused homolog |
Position | 10q24.32 |
Gene Type | protein-coding |
Gene Mutation: | PCGP germline mutation PCGP somatic mutation COSMIC somatic mutation |
PCGP germline mutation [Top] | ||
There is no record for SUFU | ||
PCGP somatic mutation [Top] | ||
Variant (Variant; Chr; Position) | Genotype (MutationType; MutationClass; ReferenceAllele; Genotype; Origin) | Disease (CancerType; ValidationStatus; SequencingType) |
|---|---|---|
SUFU_E260fs; chr10; 104356918 |
IFRAMESHIFT; -; -/AGGGA; SOMATIC | MB; VALID; WGS |
SUFU_V148_Q150fs; chr10; 104309851 |
DEL; FRAMESHIFT; GTGTTCC; GTGTTCC/-; SOMATIC | MB; VALID; WGS |
COSMIC somatic mutation [Top] | ||
Mutation (CDS; AA; Chr) | Site | Histology |
|---|---|---|
c.?; p.R146*; |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma; desmoplastic |
c.1084C>T; p.R362C; 10:104365076-104365076 |
central_nervous_system; cerebellum | primitive_neuroectodermal_tumour-medulloblastoma; large_cell |
c.591C>T; p.F197F; 10:104342465-104342465 |
skin; face | carcinoma; basal_cell_carcinoma |
c.560C>T; p.P187L; 10:104342434-104342434 |
skin; face | carcinoma; basal_cell_carcinoma |
c.896G>A; p.R299Q; |
breast | carcinoma; HER-positive_carcinoma |
c.113A>G; p.Y38C; |
endometrium | carcinoma; endometrioid_carcinoma |
c.1022+1G>A; p.?; 10:104349292-104349292 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma; desmoplastic |
c.1129_1135delTCCGGAG; p.S377fs*7; 10:104365121-104365127 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma; desmoplastic |
c.1232C>T; p.T411M; |
pleura | mesothelioma |
c.1157+1G>A; p.?; |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma |
c.881_882insG; p.T295fs*56; |
NS | NS |
c.1123C>T; p.Q375*; |
bone | chondrosarcoma |
c.778_779insAGGGA; p.T261fs*8; |
central_nervous_system; cerebellum | primitive_neuroectodermal_tumour-medulloblastoma; SHH_subtype |
c.442_448delGTGTTCC; p.V148fs*30; |
central_nervous_system; cerebellum | primitive_neuroectodermal_tumour-medulloblastoma; SHH_subtype |
c.598-1G>C; p.?; |
lung | carcinoma; squamous_cell_carcinoma |
c.850G>T; p.D284Y; |
lung; right_lower_lobe | carcinoma; adenocarcinoma |
c.63T>A; p.T21T; |
lung; right_upper_lobe | carcinoma; adenocarcinoma |
c.671G>A; p.R224Q; |
lung | carcinoma; squamous_cell_carcinoma |
c.1016G>C; p.R339P; |
ovary | carcinoma; serous_carcinoma |
c.486C>A; p.S162S; |
lung | carcinoma; squamous_cell_carcinoma |
c.1091G>A; p.R364Q; |
kidney | carcinoma; clear_cell_renal_cell_carcinoma |
c.1022+1G>A; p.?; 10:104349292-104349292 |
endometrium | carcinoma; endometrioid_carcinoma |
c.1232C>T; p.T411M; |
large_intestine; colon | carcinoma; adenocarcinoma |
c.64_65insC; p.A25fs*23; |
large_intestine; colon | carcinoma; adenocarcinoma |
c.220T>C; p.Y74H; |
large_intestine; caecum | carcinoma; adenocarcinoma |
c.847G>A; p.E283K; |
breast | carcinoma |
c.1437C>T; p.F479F; |
endometrium | carcinoma; endometrioid_carcinoma |
c.442G>A; p.V148M; |
endometrium | carcinoma; endometrioid_carcinoma |
c.1022+1G>A; p.?; 10:104349292-104349292 |
large_intestine; colon | carcinoma; adenocarcinoma |
c.778G>A; p.E260K; |
endometrium | carcinoma; endometrioid_carcinoma |
c.1005C>T; p.L335L; |
endometrium | carcinoma; endometrioid_carcinoma |
c.1309G>A; p.E437K; |
breast | carcinoma |
c.433G>A; p.A145T; |
endometrium | carcinoma; endometrioid_carcinoma |
c.1177C>T; p.R393W; |
endometrium | carcinoma; endometrioid_carcinoma |
c.1174G>T; p.G392*; |
endometrium | carcinoma; endometrioid_carcinoma |
c.1085G>A; p.R362H; |
large_intestine; caecum | carcinoma; adenocarcinoma |
c.742G>A; p.D248N; |
urinary_tract; bladder | carcinoma |
c.395C>G; p.A132G; |
prostate | carcinoma; adenocarcinoma |
c.1241A>G; p.E414G; |
prostate | carcinoma |
c.1069C>T; p.P357S; |
skin | malignant_melanoma |
c.1085G>A; p.R362H; |
skin | malignant_melanoma |
c.1136C>T; p.A379V; |
skin | malignant_melanoma |
c.1429G>C; p.V477L; |
kidney | carcinoma; clear_cell_renal_cell_carcinoma |
c.881G>A; p.G294D; |
kidney | carcinoma; clear_cell_renal_cell_carcinoma |