Entrez Gene

Basic Information
Gene ID	2056
Name	EPO

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.525C>T; p.F175F; 7:100723076-100723076	skin	malignant_melanoma	Substitution - coding silent
c.553G>A; p.G185R; 7:100723104-100723104	skin	malignant_melanoma	Substitution - Missense
c.246+10_246+12delTTT; p.?; 7:100722058-100722060	liver	carcinoma	Unknown
c.419G>A; p.G140E; 7:100722836-100722836	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.419G>A; p.G140E; 7:100722836-100722836	skin	malignant_melanoma	Substitution - Missense
c.522T>A; p.N174K; 7:100723073-100723073	skin	malignant_melanoma	Substitution - Missense
c.497G>A; p.R166H; 7:100723048-100723048	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.335C>T; p.S112F; 7:100722752-100722752	prostate	carcinoma	Substitution - Missense
c.513C>G; p.V171V; 7:100723064-100723064	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.530G>A; p.R177Q; 7:100723081-100723081	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.276G>T; p.Q92H; 7:100722693-100722693	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.429G>A; p.K143K; 7:100722980-100722980	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.466C>T; p.P156S; 7:100723017-100723017	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.441C>T; p.S147S; 7:100722992-100722992	skin	malignant_melanoma	Substitution - coding silent
c.69C>G; p.L23L; 7:100721613-100721613	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.252G>A; p.G84G; 7:100722669-100722669	skin	malignant_melanoma	Substitution - coding silent
c.351C>A; p.P117P; 7:100722768-100722768	skin	malignant_melanoma	Substitution - coding silent
c.492T>G; p.T164T; 7:100723043-100723043	prostate	carcinoma; adenocarcinoma	Substitution - coding silent
c.529C>T; p.R177W; 7:100723080-100723080	endometrium	carcinoma; serous_carcinoma	Substitution - Missense
c.529C>T; p.R177W; 7:100723080-100723080	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.529C>T; p.R177W; 7:100723080-100723080	skin	malignant_melanoma	Substitution - Missense
c.230C>A; p.A77D; 7:100722032-100722032	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.307C>T; p.R103W; 7:100722724-100722724	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.293C>T; p.S98L; 7:100722710-100722710	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.504C>G; p.L168L; 7:100723055-100723055	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.169G>T; p.A57S; 7:100721971-100721971	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.243G>A; p.M81I; 7:100722045-100722045	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.246G>T; p.E82D; 7:100722048-100722048	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.561C>A; p.A187A; 7:100723112-100723112	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.578G>A; p.R193K; 7:100723129-100723129	urinary_tract; bladder	carcinoma; transitional_cell_carcinoma	Substitution - Missense
c.578G>A; p.R193K; 7:100723129-100723129	urinary_tract; bladder	carcinoma	Substitution - Missense
c.472C>T; p.R158*; 7:100723023-100723023	skin	malignant_melanoma	Substitution - Nonsense
c.161C>T; p.T54M; 7:100721963-100721963	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.159G>A; p.T53T; 7:100721703-100721703	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.159G>A; p.T53T; 7:100721703-100721703	lung; right_lower_lobe	carcinoma; adenocarcinoma	Substitution - coding silent
c.206C>T; p.P69L; 7:100722008-100722008	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.533G>A; p.G178E; 7:100723084-100723084	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense

The somatic mutations from COSMIC database