Entrez Gene

Basic Information
Gene ID	347736
Name	NME9
Synonymous	NME/NM23 family member 9;NME9;NME/NM23 family member 9
Definition	NME family member 9\|NME gene family member 9\|thioredoxin domain containing 6\|thioredoxin domain-containing protein 6\|thioredoxin-like 2\|thioredoxin-like protein 2
Position	3q22.3
Gene Type	protein-coding

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
COSMIC somatic mutation [Top]
c.74G>T; p.S25I; 3:138324890-138324890	liver	carcinoma	Substitution - Missense
c.123C>A; p.P41P; 3:138319550-138319550	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.690G>A; p.L230L; 3:138304974-138304974	skin	malignant_melanoma	Substitution - coding silent
c.814G>T; p.E272*; 3:138303621-138303621	large_intestine	carcinoma; adenocarcinoma	Substitution - Nonsense
c.109G>A; p.G37S; 3:138319564-138319564	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.679_680insA; p.S227fs*10; 3:138304984-138304985	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Insertion - Frameshift
c.641C>T; p.A214V; 3:138305023-138305023	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.251C>A; p.T84N; 3:138318164-138318164	central_nervous_system; brain	primitive_neuroectodermal_tumour-medulloblastoma	Substitution - Missense
c.720C>T; p.D240D; 3:138304944-138304944	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.474G>A; p.R158R; 3:138306467-138306467	skin	malignant_melanoma	Substitution - coding silent
c.208C>T; p.R70C; 3:138318207-138318207	skin	malignant_melanoma	Substitution - Missense
c.688C>T; p.L230L; 3:138304976-138304976	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.868G>A; p.E290K; 3:138303567-138303567	liver	carcinoma	Substitution - Missense
c.61G>A; p.E21K; 3:138324903-138324903	skin	malignant_melanoma	Substitution - Missense
c.162C>T; p.I54I; 3:138319511-138319511	skin	malignant_melanoma	Substitution - coding silent
c.737G>A; p.R246Q; 3:138304927-138304927	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.701G>A; p.R234K; 3:138304963-138304963	skin	malignant_melanoma	Substitution - Missense
c.223G>A; p.E75K; 3:138318192-138318192	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.793C>T; p.L265F; 3:138303642-138303642	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.608G>A; p.R203Q; 3:138306032-138306032	skin	malignant_melanoma	Substitution - Missense
c.562G>C; p.E188Q; 3:138306078-138306078	urinary_tract; bladder	carcinoma	Substitution - Missense
c.761C>T; p.P254L; 3:138304903-138304903	skin	malignant_melanoma	Substitution - Missense
c.250A>G; p.T84A; 3:138318165-138318165	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.838G>A; p.G280R; 3:138303597-138303597	skin	malignant_melanoma	Substitution - Missense
c.674G>A; p.G225E; 3:138304990-138304990	skin	malignant_melanoma	Substitution - Missense
c.742G>A; p.V248I; 3:138304922-138304922	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense

COSMIC somatic mutation [Top]