Entrez Gene

Basic Information
Gene ID	362
Name	AQP5

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.572G>A; p.G191D; 12:49964135-49964135	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.633C>T; p.I211I; 12:49965012-49965012	skin	malignant_melanoma	Substitution - coding silent
c.137C>T; p.A46V; 12:49962154-49962154	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.793C>A; p.R265S; 12:49965172-49965172	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma	Substitution - Missense
c.607C>T; p.H203Y; 12:49964170-49964170	oesophagus; lower_third	carcinoma; adenocarcinoma	Substitution - Missense
c.78C>T; p.F26F; 12:49962095-49962095	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.365T>G; p.L122R; 12:49963493-49963493	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.177C>T; p.A59A; 12:49962194-49962194	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.488T>C; p.L163P; 12:49963616-49963616	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.766C>T; p.R256W; 12:49965145-49965145	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.275C>T; p.A92V; 12:49962292-49962292	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.275C>T; p.A92V; 12:49962292-49962292	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.783G>A; p.E261E; 12:49965162-49965162	ovary	other; neoplasm	Substitution - coding silent
c.578C>T; p.A193V; 12:49964141-49964141	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.578C>T; p.A193V; 12:49964141-49964141	thyroid	carcinoma	Substitution - Missense
c.582G>A; p.V194V; 12:49964145-49964145	skin	malignant_melanoma	Substitution - coding silent
c.653C>T; p.A218V; 12:49965032-49965032	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.403G>C; p.E135Q; 12:49963531-49963531	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.22G>T; p.V8L; 12:49962039-49962039	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.304G>A; p.A102T; 12:49962321-49962321	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.380C>T; p.T127M; 12:49963508-49963508	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma	Substitution - Missense
c.595T>C; p.F199L; 12:49964158-49964158	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.40G>A; p.V14M; 12:49962057-49962057	urinary_tract; bladder	carcinoma	Substitution - Missense
c.767G>A; p.R256Q; 12:49965146-49965146	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.549C>A; p.S183S; 12:49964112-49964112	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.92C>G; p.S31W; 12:49962109-49962109	breast	carcinoma	Substitution - Missense
c.194G>A; p.G65D; 12:49962211-49962211	large_intestine; colon	carcinoma	Substitution - Missense
c.194G>A; p.G65D; 12:49962211-49962211	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.574C>T; p.P192S; 12:49964137-49964137	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.426G>C; p.L142L; 12:49963554-49963554	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.211G>T; p.A71S; 12:49962228-49962228	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.45C>T; p.F15F; 12:49962062-49962062	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - coding silent
c.27C>T; p.A9A; 12:49962044-49962044	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.46G>A; p.A16T; 12:49962063-49962063	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.292G>A; p.A98T; 12:49962309-49962309	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.107C>T; p.P36L; 12:49962124-49962124	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.739G>A; p.E247K; 12:49965118-49965118	urinary_tract; bladder	carcinoma; transitional_cell_carcinoma	Substitution - Missense
c.739G>A; p.E247K; 12:49965118-49965118	urinary_tract; bladder	carcinoma	Substitution - Missense
c.602C>A; p.P201H; 12:49964165-49964165	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.109T>C; p.S37P; 12:49962126-49962126	urinary_tract; bladder	carcinoma	Substitution - Missense

The somatic mutations from COSMIC database