Cell senescence gene database Home
Cell senescence database
General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

8342

Name

HIST1H2BM

Synonymous

histone cluster 1, H2bm;HIST1H2BM;histone cluster 1, H2bm

Definition

H2B histone family, member E|histone 1, H2bm|histone H2B type 1-M|histone H2B.e

Position

6p22.1

Gene Type

protein-coding

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.299G>A; p.R100H; 6:27815342-27815342

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.213T>C; p.F71F; 6:27815256-27815256

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.299G>A; p.R100H; 6:27815342-27815342

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.241C>T; p.L81L; 6:27815284-27815284

 livercarcinomaSubstitution - coding silent

c.241C>T; p.L81L; 6:27815284-27815284

 livercarcinomaSubstitution - coding silent

c.241C>T; p.L81L; 6:27815284-27815284

 livercarcinomaSubstitution - coding silent

c.245C>T; p.A82V; 6:27815288-27815288

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.259C>T; p.R87C; 6:27815302-27815302

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.171C>T; p.S57S; 6:27815214-27815214

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.171C>T; p.S57S; 6:27815214-27815214

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.100C>T; p.R34C; 6:27815143-27815143

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.366T>C; p.Y122Y; 6:27815409-27815409

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.199G>A; p.V67I; 6:27815242-27815242

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.67C>T; p.Q23*; 6:27815110-27815110

 breastcarcinomaSubstitution - Nonsense

c.117_118delTG; p.Y41fs*31; 6:27815160-27815161

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.177T>C; p.A59A; 6:27815220-27815220

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.177T>C; p.A59A; 6:27815220-27815220

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.77A>T; p.D26V; 6:27815120-27815120

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.291G>C; p.T97T; 6:27815334-27815334

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.239G>A; p.R80H; 6:27815282-27815282

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.249T>C; p.H83H; 6:27815292-27815292

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.249T>C; p.H83H; 6:27815292-27815292

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.238C>T; p.R80C; 6:27815281-27815281

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.158C>G; p.T53S; 6:27815201-27815201

 soft_tissue; blood_vesselangiosarcomaSubstitution - Missense

c.273T>C; p.T91T; 6:27815316-27815316

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.159C>T; p.T53T; 6:27815202-27815202

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.7G>C; p.E3Q; 6:27815050-27815050

 haematopoietic_and_lymphoid_tissue; lymph_nodelymphoid_neoplasm; diffuse_large_B_cell_lymphomaSubstitution - Missense

c.204C>T; p.N68N; 6:27815247-27815247

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.128A>G; p.Y43C; 6:27815171-27815171

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.128A>G; p.Y43C; 6:27815171-27815171

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.184A>G; p.I62V; 6:27815227-27815227

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.194C>G; p.S65C; 6:27815237-27815237

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.222C>T; p.I74I; 6:27815265-27815265

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.222C>T; p.I74I; 6:27815265-27815265

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.261C>T; p.R87R; 6:27815304-27815304

 skinmalignant_melanomaSubstitution - coding silent

c.260G>A; p.R87H; 6:27815303-27815303

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.276G>C; p.S92S; 6:27815319-27815319

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.276G>C; p.S92S; 6:27815319-27815319

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.101G>A; p.R34H; 6:27815144-27815144

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.219T>C; p.R73R; 6:27815262-27815262

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.117T>C; p.S39S; 6:27815160-27815160

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.328C>T; p.H110Y; 6:27815371-27815371

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.117T>C; p.S39S; 6:27815160-27815160

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.74_75insGGAT; p.K28fs*46; 6:27815117-27815118

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaInsertion - Frameshift

c.355G>A; p.V119I; 6:27815398-27815398

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.25C>T; p.P9S; 6:27815068-27815068

 skinmalignant_melanomaSubstitution - Missense

c.190A>C; p.N64H; 6:27815233-27815233

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.123T>C; p.Y41Y; 6:27815166-27815166

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.123T>C; p.Y41Y; 6:27815166-27815166

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.148C>T; p.H50Y; 6:27815191-27815191

 NSmalignant_melanomaSubstitution - Missense

c.371G>T; p.S124I; 6:27815414-27815414

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.278G>C; p.R93T; 6:27815321-27815321

 lungcarcinoma; adenocarcinomaSubstitution - Missense

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