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

Basic Information

Gene ID

23492

Name

CBX7

Synonymous

chromobox homolog 7;CBX7;chromobox homolog 7

Definition

chromobox protein homolog 7

Position

22q13.1

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.211A>C; p.K71Q; 22:39138671-39138671

 breastcarcinomaSubstitution - Missense

c.622C>G; p.P208A; 22:39134025-39134025

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.419G>A; p.R140H; 22:39134580-39134580

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.215G>T; p.R72I; 22:39138667-39138667

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.196_197insGAGC; p.A66fs*6; 22:39138685-39138686

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaInsertion - Frameshift

c.197_198insGAGC; p.G68fs*4; 22:39138684-39138685

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaInsertion - Frameshift

c.214_216AGA>G; p.R72fs*43; 22:39138666-39138668

 kidneycarcinoma; clear_cell_renal_cell_carcinomaComplex - frameshift

c.214_216AGA>G; p.R72fs*43; 22:39138666-39138668

 kidneycarcinoma; clear_cell_renal_cell_carcinomaComplex - frameshift

c.214_216AGA>G; p.R72fs*43; 22:39138666-39138668

 kidneycarcinoma; clear_cell_renal_cell_carcinomaComplex - frameshift

c.214_216AGA>G; p.R72fs*43; 22:39138666-39138668

 kidneycarcinoma; clear_cell_renal_cell_carcinomaComplex - frameshift

c.214_216AGA>G; p.R72fs*43; 22:39138666-39138668

 kidneycarcinoma; clear_cell_renal_cell_carcinomaComplex - frameshift

c.214_216AGA>G; p.R72fs*43; 22:39138666-39138668

 kidneycarcinoma; clear_cell_renal_cell_carcinomaComplex - frameshift

c.214_216AGA>G; p.R72fs*43; 22:39138666-39138668

 kidneycarcinoma; clear_cell_renal_cell_carcinomaComplex - frameshift

c.214_216AGA>G; p.R72fs*43; 22:39138666-39138668

 kidneycarcinoma; clear_cell_renal_cell_carcinomaComplex - frameshift

c.733C>T; p.R245*; 22:39133914-39133914

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.555G>A; p.A185A; 22:39134444-39134444

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.458G>A; p.R153H; 22:39134541-39134541

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.544G>A; p.V182I; 22:39134455-39134455

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.317C>T; p.T106M; 22:39134682-39134682

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.428G>A; p.R143Q; 22:39134571-39134571

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.105G>A; p.W35*; 22:39149797-39149797

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.476G>A; p.R159H; 22:39134523-39134523

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.689T>C; p.I230T; 22:39133958-39133958

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.678C>T; p.T226T; 22:39133969-39133969

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.561C>T; p.G187G; 22:39134438-39134438

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.232C>T; p.R78W; 22:39138650-39138650

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.38T>C; p.V13A; 22:39152407-39152407

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.194G>A; p.R65Q; 22:39138688-39138688

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.419G>A; p.R140H; 22:39134580-39134580

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.663C>A; p.T221T; 22:39133984-39133984

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.508C>T; p.R170W; 22:39134491-39134491

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.418C>T; p.R140C; 22:39134581-39134581

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.615C>T; p.A205A; 22:39134032-39134032

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.294G>T; p.K98N; 22:39134705-39134705

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.628C>T; p.P210S; 22:39134019-39134019

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.264C>A; p.D88E; 22:39134735-39134735

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.615C>A; p.A205A; 22:39134032-39134032

 ovarycarcinoma; serous_carcinomaSubstitution - coding silent

c.673A>G; p.I225V; 22:39133974-39133974

 prostateadenomaSubstitution - Missense

c.227C>G; p.P76R; 22:39138655-39138655

 prostateadenomaSubstitution - Missense

c.586C>T; p.P196S; 22:39134413-39134413

 skin; scalpcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.586C>T; p.P196S; 22:39134413-39134413

 skinmalignant_melanomaSubstitution - Missense

c.469C>T; p.P157S; 22:39134530-39134530

 skinmalignant_melanomaSubstitution - Missense

c.136G>A; p.E46K; 22:39141414-39141414

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.650C>T; p.S217L; 22:39133997-39133997

 skinmalignant_melanomaSubstitution - Missense

c.222G>A; p.P74P; 22:39138660-39138660

 skinmalignant_melanomaSubstitution - coding silent

c.629C>T; p.P210L; 22:39134018-39134018

 skinmalignant_melanomaSubstitution - Missense

c.686C>T; p.S229F; 22:39133961-39133961

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.468C>T; p.F156F; 22:39134531-39134531

 skinmalignant_melanomaSubstitution - coding silent

c.233G>A; p.R78Q; 22:39138649-39138649

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.739C>T; p.R247C; 22:39133908-39133908

 stomachcarcinoma; adenocarcinomaSubstitution - Missense