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

Basic Information

Gene ID

7528

Name

YY1

Synonymous

YY1 transcription factor;YY1;YY1 transcription factor

Definition

INO80 complex subunit S|YY-1|Yin and Yang 1 protein|delta transcription factor|transcriptional repressor protein YY1

Position

14q

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.830C>A; p.A277E; 14:100262454-100262454

 adrenal_gland; adrenal_glandadrenal_cortical_carcinoma; functioningSubstitution - Missense

c.1115C>G; p.T372R; 14:100277470-100277470

 adrenal_gland; adrenal_glandadrenal_cortical_adenoma; aldosterone_producingSubstitution - Missense

c.1069T>C; p.F357L; 14:100277424-100277424

 bone; pelvischondrosarcomaSubstitution - Missense

c.869A>G; p.D290G; 14:100274724-100274724

 breastcarcinomaSubstitution - Missense

c.1032A>C; p.Q344H; 14:100276618-100276618

 breastcarcinomaSubstitution - Missense

c.1154G>T; p.C385F; 14:100277509-100277509

 central_nervous_system; braingliomaSubstitution - Missense

c.223C>G; p.H75D; 14:100239467-100239467

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.381C>T; p.F127F; 14:100239625-100239625

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.802A>G; p.I268V; 14:100262426-100262426

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.207_209delCCA; p.H80delH; 14:100239451-100239453

 endometriumcarcinoma; endometrioid_carcinomaDeletion - In frame

c.207_209delCCA; p.H80delH; 14:100239451-100239453

 endometriumcarcinoma; endometrioid_carcinomaDeletion - In frame

c.283_284delAC; p.T95fs*52; 14:100239527-100239528

 endometriumcarcinoma; endometrioid_carcinomaDeletion - Frameshift

c.1106A>G; p.N369S; 14:100277461-100277461

 genital_tract; extragonadalgerm_cell_tumour; yolk_sac_tumourSubstitution - Missense

c.1124G>A; p.R375Q; 14:100277479-100277479

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasmSubstitution - Missense

c.759A>G; p.E253E; 14:100262383-100262383

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.117A>G; p.T39T; 14:100239361-100239361

 kidneyother; neoplasmSubstitution - coding silent

c.72C>T; p.H24H; 14:100239316-100239316

 kidneyother; neoplasmSubstitution - coding silent

c.117A>G; p.T39T; 14:100239361-100239361

 kidneyother; neoplasmSubstitution - coding silent

c.72C>T; p.H24H; 14:100239316-100239316

 kidneyother; neoplasmSubstitution - coding silent

c.422G>A; p.G141D; 14:100239666-100239666

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.422G>A; p.G141D; 14:100239666-100239666

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1124G>A; p.R375Q; 14:100277479-100277479

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1128C>T; p.I376I; 14:100277483-100277483

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.941G>T; p.R314I; 14:100276527-100276527

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.127_129delGAG; p.E43delE; 14:100239371-100239373

 large_intestine; caecumcarcinoma; adenocarcinomaDeletion - In frame

c.13G>A; p.D5N; 14:100239257-100239257

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.225T>C; p.H75H; 14:100239469-100239469

 livercarcinomaSubstitution - coding silent

c.1225A>G; p.K409E; 14:100277580-100277580

 livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.1225A>G; p.K409E; 14:100277580-100277580

 livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.228C>T; p.H76H; 14:100239472-100239472

 livercarcinomaSubstitution - coding silent

c.228C>T; p.H76H; 14:100239472-100239472

 livercarcinomaSubstitution - coding silent

c.206_207insCCA; p.H80_P81insH; 14:100239450-100239451

 livercarcinomaInsertion - In frame

c.1154G>T; p.C385F; 14:100277509-100277509

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.528C>T; p.G176G; 14:100239772-100239772

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.682delG; p.E228fs*28; 14:100262306-100262306

 lungcarcinoma; squamous_cell_carcinomaDeletion - Frameshift

c.757G>A; p.E253K; 14:100262381-100262381

 lungcarcinoid-endocrine_tumour; typicalSubstitution - Missense

c.111G>C; p.E37D; 14:100239355-100239355

 oesophagus; middle_thirdcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.498G>T; p.S166S; 14:100239742-100239742

 oesophaguscarcinomaSubstitution - coding silent

c.1103T>A; p.F368Y; 14:100277458-100277458

 pancreascarcinomaSubstitution - Missense

c.367G>A; p.A123T; 14:100239611-100239611

 prostatecarcinomaSubstitution - Missense

c.127_129delGAG; p.E43delE; 14:100239371-100239373

 prostatecarcinomaDeletion - In frame

c.759A>G; p.E253E; 14:100262383-100262383

 prostatecarcinoma; adenocarcinomaSubstitution - coding silent

c.759A>G; p.E253E; 14:100262383-100262383

 prostatecarcinoma; adenocarcinomaSubstitution - coding silent

c.1154G>T; p.C385F; 14:100277509-100277509

 skinmalignant_melanomaSubstitution - Missense

c.785C>T; p.P262L; 14:100262409-100262409

 skinmalignant_melanomaSubstitution - Missense

c.108C>T; p.I36I; 14:100239352-100239352

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.1082G>A; p.G361E; 14:100277437-100277437

 skin; facecarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.422G>A; p.G141D; 14:100239666-100239666

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1135G>A; p.G379R; 14:100277490-100277490

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.806A>G; p.D269G; 14:100262430-100262430

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.740C>T; p.S247L; 14:100262364-100262364

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.783T>C; p.P261P; 14:100262407-100262407

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.755C>T; p.S252L; 14:100262379-100262379

 thyroidother; neoplasmSubstitution - Missense

c.313C>A; p.L105M; 14:100239557-100239557

 thyroidother; neoplasmSubstitution - Missense

c.756A>C; p.S252S; 14:100262380-100262380

 thyroidother; neoplasmSubstitution - coding silent

c.757G>T; p.E253*; 14:100262381-100262381

 thyroidother; neoplasmSubstitution - Nonsense