Epithelial-Mesenchymal Transition gene database (dbEMT) Home
dbEMT
dbEMT 2.0
General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

5110

Name

PCMT1

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.503C>T; p.A168V; 6:149796499-149796499

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.503C>T; p.A168V; 6:149796499-149796499

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.628G>A; p.G210R; 6:149802323-149802323

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.184C>A; p.P62T; 6:149773161-149773161

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.361A>C; p.N121H; 6:149793612-149793612

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.357A>C; p.S119S; 6:149793608-149793608

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.293G>A; p.R98H; 6:149790054-149790054

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.455C>A; p.P152H; 6:149796451-149796451

thyroidother; neoplasmSubstitution - Missense

c.615G>T; p.M205I; 6:149802310-149802310

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.561C>T; p.G187G; 6:149802256-149802256

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.168A>G; p.Q56Q; 6:149773145-149773145

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.362A>G; p.N121S; 6:149793613-149793613

livercarcinomaSubstitution - Missense

c.362A>G; p.N121S; 6:149793613-149793613

livercarcinomaSubstitution - Missense

c.401G>A; p.G134E; 6:149793652-149793652

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.82G>C; p.V28L; 6:149771188-149771188

breastcarcinomaSubstitution - Missense

c.375G>T; p.K125N; 6:149793626-149793626

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.241A>G; p.K81E; 6:149790002-149790002

central_nervous_system; braingliomaSubstitution - Missense

c.378C>T; p.D126D; 6:149793629-149793629

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.108C>T; p.D36D; 6:149771214-149771214

ovarycarcinoma; serous_carcinomaSubstitution - coding silent

c.251A>T; p.D84V; 6:149790012-149790012

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.251A>T; p.D84V; 6:149790012-149790012

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.358G>A; p.V120I; 6:149793609-149793609

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.562G>T; p.G188*; 6:149802257-149802257

prostateadenomaSubstitution - Nonsense

c.602G>A; p.G201D; 6:149802297-149802297

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.131A>T; p.N44I; 6:149771237-149771237

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense


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