General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 8991 |
Name | SELENBP1 |
Synonymous | selenium binding protein 1;SELENBP1;selenium binding protein 1 |
Definition | 56 kDa selenium-binding protein|epididymis secretory sperm binding protein Li 134P|selenium-binding protein 1 |
Position | 1q21.3 |
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 0.06. |
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.1058G>A; p.G353D; 1:151365268-151365268 |
oesophagus; upper_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1146G>A; p.R382R; 1:151365036-151365036 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.555G>A; p.P185P; 1:151366831-151366831 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.192C>T; p.P64P; 1:151369172-151369172 |
skin | malignant_melanoma | Substitution - coding silent |
c.1317C>G; p.N439K; 1:151364645-151364645 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.584G>A; p.R195Q; 1:151366802-151366802 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.584G>A; p.R195Q; 1:151366802-151366802 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.584G>A; p.R195Q; 1:151366802-151366802 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1362C>T; p.A454A; 1:151364600-151364600 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.340C>T; p.R114W; 1:151369024-151369024 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1357C>T; p.P453S; 1:151364605-151364605 |
skin | malignant_melanoma | Substitution - Missense |
c.6T>G; p.A2A; 1:151369768-151369768 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.715G>T; p.V239L; 1:151366403-151366403 |
breast | carcinoma | Substitution - Missense |
c.1341G>A; p.G447G; 1:151364621-151364621 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.381C>T; p.I127I; 1:151368299-151368299 |
skin | malignant_melanoma | Substitution - coding silent |
c.748C>T; p.P250S; 1:151366370-151366370 |
skin | malignant_melanoma | Substitution - Missense |
c.748C>T; p.P250S; 1:151366370-151366370 |
skin | malignant_melanoma | Substitution - Missense |
c.1255A>G; p.R419G; 1:151364927-151364927 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.879G>A; p.V293V; 1:151365811-151365811 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.131T>A; p.L44Q; 1:151369485-151369485 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1387G>A; p.G463R; 1:151364575-151364575 |
NS | malignant_melanoma | Substitution - Missense |
c.1387G>A; p.G463R; 1:151364575-151364575 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; hairy_cell_leukaemia | Substitution - Missense |
c.1387G>A; p.G463R; 1:151364575-151364575 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; hairy_cell_leukaemia | Substitution - Missense |
c.882C>T; p.P294P; 1:151365808-151365808 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1374G>A; p.E458E; 1:151364588-151364588 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.410A>C; p.H137P; 1:151368270-151368270 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1145G>A; p.R382Q; 1:151365037-151365037 |
skin | malignant_melanoma | Substitution - Missense |
c.1249C>G; p.L417V; 1:151364933-151364933 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.696C>T; p.D232D; 1:151366422-151366422 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.1144C>T; p.R382W; 1:151365038-151365038 |
oesophagus | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.297C>A; p.L99L; 1:151369067-151369067 |
autonomic_ganglia | neuroblastoma | Substitution - coding silent |
c.184C>T; p.R62W; 1:151369180-151369180 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1173G>C; p.Q391H; 1:151365009-151365009 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.453C>T; p.S151S; 1:151368227-151368227 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.704G>A; p.R235H; 1:151366414-151366414 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1165A>G; p.M389V; 1:151365017-151365017 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.157T>C; p.S53P; 1:151369459-151369459 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.870G>A; p.V290V; 1:151365820-151365820 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1032C>T; p.R344R; 1:151365575-151365575 |
skin | malignant_melanoma | Substitution - coding silent |
c.1099G>A; p.E367K; 1:151365227-151365227 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1110G>C; p.K370N; 1:151365216-151365216 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.710A>G; p.E237G; 1:151366408-151366408 |
skin | malignant_melanoma | Substitution - Missense |
c.642C>T; p.F214F; 1:151366744-151366744 |
skin | malignant_melanoma | Substitution - coding silent |
c.642C>T; p.F214F; 1:151366744-151366744 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.552A>G; p.A184A; 1:151366834-151366834 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.933C>T; p.T311T; 1:151365674-151365674 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.761G>A; p.R254H; 1:151366357-151366357 |
liver | carcinoma | Substitution - Missense |
c.779A>T; p.D260V; 1:151366339-151366339 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.761G>A; p.R254H; 1:151366357-151366357 |
liver | carcinoma | Substitution - Missense |
c.1031G>A; p.R344H; 1:151365576-151365576 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.899G>A; p.G300D; 1:151365791-151365791 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.827G>T; p.R276L; 1:151366291-151366291 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.954C>T; p.D318D; 1:151365653-151365653 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1258G>A; p.E420K; 1:151364704-151364704 |
skin | malignant_melanoma | Substitution - Missense |
c.110G>A; p.G37D; 1:151369506-151369506 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.910C>G; p.P304A; 1:151365780-151365780 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.1408A>C; p.I470L; 1:151364554-151364554 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1232A>C; p.K411T; 1:151364950-151364950 |
kidney | other; neoplasm | Substitution - Missense |
c.252C>T; p.F84F; 1:151369112-151369112 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.9G>A; p.T3T; 1:151369765-151369765 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.412A>C; p.T138P; 1:151368268-151368268 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - Missense |
c.412A>C; p.T138P; 1:151368268-151368268 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.884C>T; p.P295L; 1:151365806-151365806 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.688G>A; p.V230I; 1:151366430-151366430 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1193G>A; p.R398H; 1:151364989-151364989 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1193G>A; p.R398H; 1:151364989-151364989 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.913G>A; p.E305K; 1:151365777-151365777 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1193G>A; p.R398H; 1:151364989-151364989 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1193G>A; p.R398H; 1:151364989-151364989 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.433G>T; p.G145W; 1:151368247-151368247 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1061G>T; p.S354I; 1:151365265-151365265 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.588C>T; p.H196H; 1:151366798-151366798 |
stomach | adenocarcinoma | Substitution - coding silent |
c.1332G>A; p.V444V; 1:151364630-151364630 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.990G>T; p.G330G; 1:151365617-151365617 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.486T>G; p.G162G; 1:151366900-151366900 |
pancreas | carcinoma | Substitution - coding silent |
c.302C>T; p.S101F; 1:151369062-151369062 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1303G>T; p.G435W; 1:151364659-151364659 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.805G>A; p.A269T; 1:151366313-151366313 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.805G>A; p.A269T; 1:151366313-151366313 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1265C>T; p.S422F; 1:151364697-151364697 |
skin | malignant_melanoma | Substitution - Missense |
c.1317_1318insGTTGAAC; p.P440fs*21; 1:151364644-151364645 |
lung | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.341G>T; p.R114L; 1:151369023-151369023 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.482G>C; p.G161A; 1:151366904-151366904 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.30C>G; p.P10P; 1:151369744-151369744 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1093G>T; p.E365*; 1:151365233-151365233 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.1407C>A; p.D469E; 1:151364555-151364555 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.760C>T; p.R254C; 1:151366358-151366358 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.614C>A; p.A205E; 1:151366772-151366772 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.220C>G; p.H74D; 1:151369144-151369144 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.742C>T; p.L248F; 1:151366376-151366376 |
skin | malignant_melanoma | Substitution - Missense |
c.827G>A; p.R276H; 1:151366291-151366291 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.5-4A>T; p.?; 1:151369773-151369773 |
thyroid | other; neoplasm | Unknown |
c.338C>T; p.P113L; 1:151369026-151369026 |
skin | malignant_melanoma | Substitution - Missense |
c.1338C>T; p.F446F; 1:151364624-151364624 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |