General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
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---|---|
Gene ID | 7476 |
Name | WNT7A |
Synonymous | wingless-type MMTV integration site family, member 7A;WNT7A;wingless-type MMTV integration site family, member 7A |
Definition | protein Wnt-7a|proto-oncogene Wnt7a protein |
Position | 3p25 |
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 0.10. |
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.873C>T; p.G291G; 3:13819121-13819121 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.241C>T; p.R81C; 3:13875004-13875004 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.150G>C; p.A50A; 3:13875095-13875095 |
skin | malignant_melanoma | Substitution - coding silent |
c.1032G>A; p.E344E; 3:13818962-13818962 |
skin | malignant_melanoma | Substitution - coding silent |
c.706G>A; p.V236I; 3:13819288-13819288 |
breast | carcinoma | Substitution - Missense |
c.706G>A; p.V236I; 3:13819288-13819288 |
breast | carcinoma | Substitution - Missense |
c.314C>A; p.A105E; 3:13854788-13854788 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.441G>A; p.W147*; 3:13854661-13854661 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; hairy_cell_leukaemia | Substitution - Nonsense |
c.441G>A; p.W147*; 3:13854661-13854661 |
NS | malignant_melanoma | Substitution - Nonsense |
c.877G>A; p.A293T; 3:13819117-13819117 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.921G>T; p.M307I; 3:13819073-13819073 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.476G>A; p.G159D; 3:13854626-13854626 |
skin | malignant_melanoma | Substitution - Missense |
c.231C>T; p.F77F; 3:13875014-13875014 |
skin | malignant_melanoma | Substitution - coding silent |
c.921G>T; p.M307I; 3:13819073-13819073 |
breast | carcinoma | Substitution - Missense |
c.51C>A; p.G17G; 3:13879766-13879766 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.315G>A; p.A105A; 3:13854787-13854787 |
breast | carcinoma | Substitution - coding silent |
c.315G>A; p.A105A; 3:13854787-13854787 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.315G>A; p.A105A; 3:13854787-13854787 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.61C>T; p.L21F; 3:13879756-13879756 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.286G>A; p.E96K; 3:13874959-13874959 |
skin | malignant_melanoma | Substitution - Missense |
c.832T>A; p.C278S; 3:13819162-13819162 |
NS | malignant_melanoma | Substitution - Missense |
c.906C>T; p.S302S; 3:13819088-13819088 |
pancreas | carcinoma | Substitution - coding silent |
c.1038C>A; p.Y346*; 3:13818956-13818956 |
breast | carcinoma | Substitution - Nonsense |
c.99C>T; p.G33G; 3:13875146-13875146 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.782G>A; p.R261H; 3:13819212-13819212 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.782G>A; p.R261H; 3:13819212-13819212 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.790A>T; p.M264L; 3:13819204-13819204 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.123C>A; p.I41I; 3:13875122-13875122 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.821C>T; p.S274L; 3:13819173-13819173 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.553A>T; p.N185Y; 3:13854549-13854549 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.305G>C; p.R102P; 3:13854797-13854797 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.353C>T; p.A118V; 3:13854749-13854749 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.595G>C; p.E199Q; 3:13819399-13819399 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.232C>T; p.R78C; 3:13875013-13875013 |
skin | malignant_melanoma | Substitution - Missense |
c.907G>A; p.G303S; 3:13819087-13819087 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.214G>A; p.E72K; 3:13875031-13875031 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.214G>A; p.E72K; 3:13875031-13875031 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.734G>A; p.R245H; 3:13819260-13819260 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.576G>A; p.L192L; 3:13819418-13819418 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.911G>C; p.C304S; 3:13819083-13819083 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.889A>C; p.T297P; 3:13819105-13819105 |
skin | malignant_melanoma | Substitution - Missense |
c.324C>T; p.Y108Y; 3:13854778-13854778 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.629C>G; p.T210S; 3:13819365-13819365 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.707T>C; p.V236A; 3:13819287-13819287 |
skin | malignant_melanoma | Substitution - Missense |
c.202A>C; p.M68L; 3:13875043-13875043 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.387C>T; p.S129S; 3:13854715-13854715 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.502G>T; p.D168Y; 3:13854600-13854600 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.922T>A; p.C308S; 3:13819072-13819072 |
breast | carcinoma | Substitution - Missense |
c.137C>T; p.P46L; 3:13875108-13875108 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.699C>T; p.N233N; 3:13819295-13819295 |
skin | malignant_melanoma | Substitution - coding silent |
c.977G>T; p.C326F; 3:13819017-13819017 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.204G>T; p.M68I; 3:13875041-13875041 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.955G>T; p.A319S; 3:13819039-13819039 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1013C>T; p.T338M; 3:13818981-13818981 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1013C>T; p.T338M; 3:13818981-13818981 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.555C>T; p.N185N; 3:13854547-13854547 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.352G>A; p.A118T; 3:13854750-13854750 |
upper_aerodigestive_tract; pharynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.529_530CG>AT; p.R177M; 3:13854572-13854573 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.555C>T; p.N185N; 3:13854547-13854547 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.304C>T; p.R102W; 3:13854798-13854798 |
skin | malignant_melanoma | Substitution - Missense |
c.304C>T; p.R102W; 3:13854798-13854798 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1041G>A; p.T347T; 3:13818953-13818953 |
pancreas | carcinoma | Substitution - coding silent |
c.788C>T; p.P263L; 3:13819206-13819206 |
skin | malignant_melanoma | Substitution - Missense |
c.155G>C; p.C52S; 3:13875090-13875090 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1025G>A; p.R342H; 3:13818969-13818969 |
liver | carcinoma | Substitution - Missense |
c.526G>T; p.A176S; 3:13854576-13854576 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.100G>A; p.A34T; 3:13875145-13875145 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.474C>T; p.Y158Y; 3:13854628-13854628 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.459T>C; p.S153S; 3:13854643-13854643 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.459T>C; p.S153S; 3:13854643-13854643 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.171C>T; p.D57D; 3:13875074-13875074 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.667G>T; p.E223*; 3:13819327-13819327 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.724C>T; p.R242C; 3:13819270-13819270 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.492G>T; p.K164N; 3:13854610-13854610 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.226C>T; p.Q76*; 3:13875019-13875019 |
urinary_tract; bladder | carcinoma | Substitution - Nonsense |
c.600T>G; p.C200W; 3:13819394-13819394 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.984C>T; p.F328F; 3:13819010-13819010 |
breast | carcinoma | Substitution - coding silent |
c.984C>T; p.F328F; 3:13819010-13819010 |
skin | malignant_melanoma | Substitution - coding silent |
c.299-4G>A; p.?; 3:13854807-13854807 |
pancreas | carcinoma | Unknown |
c.612C>T; p.G204G; 3:13819382-13819382 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.57C>G; p.V19V; 3:13879760-13879760 |
breast | carcinoma | Substitution - coding silent |
c.495C>T; p.V165V; 3:13854607-13854607 |
breast | carcinoma | Substitution - coding silent |
c.150G>A; p.A50A; 3:13875095-13875095 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.381C>T; p.N127N; 3:13854721-13854721 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.822G>A; p.S274S; 3:13819172-13819172 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.822G>A; p.S274S; 3:13819172-13819172 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.535C>G; p.L179V; 3:13854567-13854567 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.623C>T; p.S208L; 3:13819371-13819371 |
skin | malignant_melanoma | Substitution - Missense |
c.36C>G; p.L12L; 3:13879781-13879781 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.547C>T; p.H183Y; 3:13854555-13854555 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.679G>A; p.V227M; 3:13819315-13819315 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.388G>A; p.D130N; 3:13854714-13854714 |
breast | carcinoma | Substitution - Missense |
c.268C>T; p.R90C; 3:13874977-13874977 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.745C>T; p.P249S; 3:13819249-13819249 |
parathyroid | adenoma | Substitution - Missense |
c.277T>C; p.F93L; 3:13874968-13874968 |
skin | malignant_melanoma | Substitution - Missense |
c.639G>A; p.T213T; 3:13819355-13819355 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.169G>A; p.D57N; 3:13875076-13875076 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.989G>A; p.W330*; 3:13819005-13819005 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1046_1047insA; p.*350fs?; 3:13818947-13818948 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.513G>T; p.E171D; 3:13854589-13854589 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.274G>A; p.V92I; 3:13874971-13874971 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.365C>G; p.A122G; 3:13854737-13854737 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.511G>T; p.E171*; 3:13854591-13854591 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.314C>T; p.A105V; 3:13854788-13854788 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.440G>A; p.W147*; 3:13854662-13854662 |
skin; scalp | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.273C>G; p.T91T; 3:13874972-13874972 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.246G>A; p.W82*; 3:13874999-13874999 |
skin | malignant_melanoma | Substitution - Nonsense |
c.246G>A; p.W82*; 3:13874999-13874999 |
skin | malignant_melanoma | Substitution - Nonsense |
c.269G>T; p.R90L; 3:13874976-13874976 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.487G>A; p.A163T; 3:13854615-13854615 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1024C>T; p.R342C; 3:13818970-13818970 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1024C>T; p.R342C; 3:13818970-13818970 |
peritoneum; appendix | other; pseudomyxoma_peritonei | Substitution - Missense |
c.487G>A; p.A163T; 3:13854615-13854615 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.565C>T; p.R189*; 3:13854537-13854537 |
skin | malignant_melanoma | Substitution - Nonsense |
c.516C>G; p.I172M; 3:13854586-13854586 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.687G>A; p.K229K; 3:13819307-13819307 |
skin | malignant_melanoma | Substitution - coding silent |
c.463G>A; p.D155N; 3:13854639-13854639 |
skin | malignant_melanoma | Substitution - Missense |
c.180C>T; p.I60I; 3:13875065-13875065 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.463G>A; p.D155N; 3:13854639-13854639 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.469C>T; p.R157C; 3:13854633-13854633 |
skin; upper_leg | malignant_melanoma | Substitution - Missense |
c.853G>A; p.G285S; 3:13819141-13819141 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.340G>T; p.G114C; 3:13854762-13854762 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.868C>A; p.Q290K; 3:13819126-13819126 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.934G>A; p.G312S; 3:13819060-13819060 |
skin | malignant_melanoma | Substitution - Missense |
c.934G>A; p.G312S; 3:13819060-13819060 |
skin | malignant_melanoma | Substitution - Missense |
c.282delG; p.K95fs*34; 3:13874963-13874963 |
breast | carcinoma | Deletion - Frameshift |
c.117C>A; p.N39K; 3:13875128-13875128 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.208C>T; p.L70L; 3:13875037-13875037 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.700G>A; p.E234K; 3:13819294-13819294 |
breast | carcinoma | Substitution - Missense |
c.944C>T; p.T315I; 3:13819050-13819050 |
skin | malignant_melanoma | Substitution - Missense |
c.280G>A; p.G94R; 3:13874965-13874965 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - Missense |