General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 3622 |
Name | ING2 |
Synonymous | inhibitor of growth family, member 2;ING2;inhibitor of growth family, member 2 |
Definition | ING1Lp|inhibitor of growth 1-like protein|inhibitor of growth protein 2|p32 |
Position | 4q35.1 |
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 0.20. |
The copy number variations for various cancers | Top |
There is no record for ING2 |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) |
Site |
Histology |
Mutation Type |
---|---|---|---|
c.457C>A; p.R153S; 4:183510566-183510566 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.457C>A; p.R153S; 4:183510566-183510566 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.759G>C; p.W253C; 4:183510868-183510868 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.786T>A; p.N262K; 4:183510895-183510895 |
skin | malignant_melanoma | Substitution - Missense |
c.445T>C; p.S149P; 4:183510554-183510554 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.515A>C; p.D172A; 4:183510624-183510624 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.325G>T; p.E109*; 4:183510434-183510434 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.278G>C; p.S93T; 4:183510387-183510387 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.340C>T; p.R114W; 4:183510449-183510449 |
skin | malignant_melanoma | Substitution - Missense |
c.39C>T; p.A13A; 4:183505234-183505234 |
breast | carcinoma | Substitution - coding silent |
c.39C>T; p.A13A; 4:183505234-183505234 |
thyroid | other; neoplasm | Substitution - coding silent |
c.398G>A; p.R133Q; 4:183510507-183510507 |
oesophagus | carcinoma | Substitution - Missense |
c.819delA; p.K275fs*>6; 4:183510928-183510928 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.514G>T; p.D172Y; 4:183510623-183510623 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.642C>G; p.Y214*; 4:183510751-183510751 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Nonsense |
c.759G>T; p.W253C; 4:183510868-183510868 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.266C>T; p.A89V; 4:183510375-183510375 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.475G>A; p.E159K; 4:183510584-183510584 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.202G>A; p.E68K; 4:183510311-183510311 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.202G>A; p.E68K; 4:183510311-183510311 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.200A>G; p.Y67C; 4:183510309-183510309 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.758G>A; p.W253*; 4:183510867-183510867 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.758G>A; p.W253*; 4:183510867-183510867 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.760T>C; p.Y254H; 4:183510869-183510869 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.605C>T; p.P202L; 4:183510714-183510714 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.309T>A; p.I103I; 4:183510418-183510418 |
skin | malignant_melanoma | Substitution - coding silent |
c.245T>C; p.L82P; 4:183510354-183510354 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.749A>G; p.K250R; 4:183510858-183510858 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.116_117CC>TT; p.P39L; 4:183505311-183505312 |
skin | malignant_melanoma | Substitution - Missense |
c.412G>C; p.A138P; 4:183510521-183510521 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.679G>A; p.G227R; 4:183510788-183510788 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.467G>C; p.R156P; 4:183510576-183510576 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.120C>G; p.H40Q; 4:183505315-183505315 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.120C>G; p.H40Q; 4:183505315-183505315 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.745C>T; p.P249S; 4:183510854-183510854 |
skin | malignant_melanoma | Substitution - Missense |
c.602C>T; p.S201L; 4:183510711-183510711 |
breast | carcinoma | Substitution - Missense |
c.54G>A; p.G18G; 4:183505249-183505249 |
pancreas | carcinoma | Substitution - coding silent |
c.610G>C; p.E204Q; 4:183510719-183510719 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.469A>T; p.T157S; 4:183510578-183510578 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.778G>T; p.G260*; 4:183510887-183510887 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |