Entrez Gene

Basic Information
Gene ID	27035
Name	NOX1

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.153C>A; p.A51A; 23:100863584-100863584	pancreas	carcinoma	Substitution - coding silent
c.211G>A; p.V71M; 23:100863526-100863526	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.449A>G; p.K150R; 23:100862709-100862709	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.128G>C; p.R43T; 23:100870732-100870732	skin	malignant_melanoma	Substitution - Missense
c.240G>C; p.R80S; 23:100863497-100863497	skin	malignant_melanoma	Substitution - Missense
c.444G>A; p.E148E; 23:100862714-100862714	skin; head_neck	malignant_melanoma; superficial_spreading	Substitution - coding silent
c.218G>A; p.R73H; 23:100863519-100863519	cervix	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.105G>A; p.K35K; 23:100870755-100870755	skin	malignant_melanoma	Substitution - coding silent
c.389G>A; p.R130Q; 23:100862769-100862769	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.321G>A; p.M107I; 23:100863175-100863175	skin	malignant_melanoma	Substitution - Missense
c.73C>T; p.L25L; 23:100870787-100870787	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.27G>A; p.W9*; 23:100874113-100874113	large_intestine	carcinoma; adenocarcinoma	Substitution - Nonsense
c.300C>A; p.F100L; 23:100863196-100863196	skin; trunk	malignant_melanoma	Substitution - Missense
c.106G>A; p.A36T; 23:100870754-100870754	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.136C>T; p.L46F; 23:100870724-100870724	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.136C>T; p.L46F; 23:100870724-100870724	skin	malignant_melanoma	Substitution - Missense
c.286C>T; p.H96Y; 23:100863210-100863210	skin	malignant_melanoma	Substitution - Missense
c.263G>A; p.R88H; 23:100863233-100863233	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.263G>A; p.R88H; 23:100863233-100863233	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.251C>T; p.S84L; 23:100863486-100863486	urinary_tract; bladder	carcinoma	Substitution - Missense
c.94A>C; p.K32Q; 23:100870766-100870766	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.390A>G; p.R130R; 23:100862768-100862768	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.135C>T; p.I45I; 23:100870725-100870725	skin	malignant_melanoma	Substitution - coding silent
c.285T>C; p.D95D; 23:100863211-100863211	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.46-1G>T; p.?; 23:100870815-100870815	lung	carcinoma; adenocarcinoma	Unknown
c.209C>A; p.P70H; 23:100863528-100863528	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.241G>A; p.G81S; 23:100863496-100863496	skin	malignant_melanoma	Substitution - Missense
c.134T>A; p.I45N; 23:100870726-100870726	lung	carcinoid-endocrine_tumour; atypical	Substitution - Missense
c.213G>C; p.V71V; 23:100863524-100863524	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.421C>A; p.L141I; 23:100862737-100862737	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.394G>A; p.A132T; 23:100862764-100862764	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.50T>C; p.V17A; 23:100870810-100870810	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.195G>A; p.T65T; 23:100863542-100863542	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.408C>T; p.S136S; 23:100862750-100862750	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - coding silent
c.139G>A; p.G47R; 23:100870721-100870721	skin	malignant_melanoma	Substitution - Missense
c.388C>A; p.R130R; 23:100862770-100862770	ovary	carcinoma; serous_carcinoma	Substitution - coding silent
c.388C>A; p.R130R; 23:100862770-100862770	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.476+6G>A; p.?; 23:100862676-100862676	lung	carcinoma; small_cell_carcinoma	Unknown
c.534C>T; p.S178S; 23:100843390-100843390	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent

The somatic mutations from COSMIC database