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

Basic Information

Gene ID

3021

Name

H3F3B

Synonymous

H3 histone, family 3B (H3.3B);H3F3B;H3 histone, family 3B (H3.3B)

Definition

histone H3.3

Position

17q25.1

Gene Type

protein-coding

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.358A>G; p.I120V; 17:75778648-75778648

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.128G>A; p.R43K; 17:75779047-75779047

skin; extremitymalignant_melanomaSubstitution - Missense

c.91C>T; p.P31S; 17:75779084-75779084

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.52_53insC; p.R18fs*80; 17:75779122-75779123

ovarycarcinoma; serous_carcinomaInsertion - Frameshift

c.128+1G>T; p.?; 17:75779046-75779046

endometriumcarcinoma; endometrioid_carcinomaUnknown

c.52_53insC; p.R18fs*80; 17:75779122-75779123

large_intestine; coloncarcinoma; adenocarcinomaInsertion - Frameshift

c.111G>C; p.K37N; 17:75779064-75779064

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.315C>G; p.F105L; 17:75778691-75778691

ovarycarcinoma; clear_cell_carcinomaSubstitution - Missense

c.400G>C; p.E134Q; 17:75778606-75778606

urinary_tract; bladdercarcinomaSubstitution - Missense

c.260G>T; p.S87I; 17:75778832-75778832

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.92C>T; p.P31L; 17:75779083-75779083

skin; mucosalmalignant_melanomaSubstitution - Missense

c.79A>G; p.R27G; 17:75779096-75779096

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.204C>T; p.F68F; 17:75778888-75778888

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.32_33CC>TT; p.S11F; 17:75779142-75779143

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.204C>T; p.F68F; 17:75778888-75778888

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.50C>T; p.P17L; 17:75779125-75779125

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.50C>T; p.P17L; 17:75779125-75779125

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.197_275del79; p.L66fs*>45; 17:75778817-75778895

stomachcarcinoma; intestinal_adenocarcinomaDeletion - Frameshift

c.149G>C; p.R50P; 17:75778943-75778943

urinary_tract; bladdercarcinomaSubstitution - Missense

c.97A>T; p.T33S; 17:75779078-75779078

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.262G>A; p.A88T; 17:75778830-75778830

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.270C>A; p.I90I; 17:75778822-75778822

urinary_tract; bladdercarcinomaSubstitution - coding silent

c.270C>A; p.I90I; 17:75778822-75778822

urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - coding silent

c.110A>T; p.K37M; 17:75779065-75779065

bone; humerusother; chondroblastomaSubstitution - Missense

c.110A>T; p.K37M; 17:75779065-75779065

bone; femurother; chondroblastomaSubstitution - Missense

c.110A>T; p.K37M; 17:75779065-75779065

bone; femurother; chondroblastomaSubstitution - Missense

c.110A>T; p.K37M; 17:75779065-75779065

bone; humerusother; chondroblastomaSubstitution - Missense

c.163T>A; p.Y55N; 17:75778929-75778929

skinmalignant_melanomaSubstitution - Missense

c.319G>A; p.D107N; 17:75778687-75778687

skinmalignant_melanomaSubstitution - Missense


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