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Gene information | Literature | Expression | lncRNA | Mutation | Homolog

Basic Information

Gene ID

51053

Name

GMNN

Synonymous

geminin, DNA replication inhibitor;GMNN;geminin, DNA replication inhibitor

Definition

geminin

Position

6p22.3

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.352G>C; p.E118Q; 6:24784164-24784164

 breastcarcinomaSubstitution - Missense

c.558G>T; p.V186V; 6:24785727-24785727

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.310G>C; p.E104Q; 6:24784122-24784122

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.479G>A; p.G160D; 6:24785648-24785648

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.295T>C; p.W99R; 6:24784107-24784107

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.296G>A; p.W99*; 6:24784108-24784108

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.296G>A; p.W99*; 6:24784108-24784108

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.51+2T>C; p.?; 6:24777299-24777299

 large_intestine; coloncarcinoma; adenocarcinomaUnknown

c.579G>A; p.T193T; 6:24785748-24785748

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.609G>A; p.T203T; 6:24785778-24785778

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.58T>C; p.S20P; 6:24780669-24780669

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.58T>C; p.S20P; 6:24780669-24780669

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.31G>T; p.E11*; 6:24777277-24777277

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.469-1G>T; p.?; 6:24785637-24785637

 large_intestine; coloncarcinoma; adenocarcinomaUnknown

c.567A>C; p.S189S; 6:24785736-24785736

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.198G>T; p.G66G; 6:24781545-24781545

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.18G>A; p.K6K; 6:24777264-24777264

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.296G>T; p.W99L; 6:24784108-24784108

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.230A>G; p.N77S; 6:24781577-24781577

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.605C>T; p.S202F; 6:24785774-24785774

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.119G>A; p.R40K; 6:24780730-24780730

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.188C>G; p.S63C; 6:24781535-24781535

 oesophagus; lower_thirdcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.297G>T; p.W99C; 6:24784109-24784109

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.293A>T; p.Y98F; 6:24784105-24784105

 pancreasother; pancreatoblastomaSubstitution - Missense

c.130C>T; p.L44L; 6:24781477-24781477

 pancreascarcinoma; ductal_carcinomaSubstitution - coding silent

c.310G>C; p.E104Q; 6:24784122-24784122

 prostatecarcinomaSubstitution - Missense

c.445C>T; p.Q149*; 6:24784531-24784531

 skin; extremitymalignant_melanomaSubstitution - Nonsense

c.207C>T; p.V69V; 6:24781554-24781554

 skinmalignant_melanomaSubstitution - coding silent

c.52-1G>C; p.?; 6:24780662-24780662

 skin; head_neckcarcinoma; squamous_cell_carcinomaUnknown

c.367G>T; p.E123*; 6:24784453-24784453

 stomachcarcinoma; adenocarcinomaSubstitution - Nonsense

c.178T>C; p.S60P; 6:24781525-24781525

 stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.53A>C; p.N18T; 6:24780664-24780664

 thyroidother; neoplasmSubstitution - Missense