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

Basic Information

Gene ID

6659

Name

SOX4

Synonymous

SRY (sex determining region Y)-box 4;SOX4;SRY (sex determining region Y)-box 4

Definition

SRY-related HMG-box gene 4|ecotropic viral integration site 16|transcription factor SOX-4

Position

6p22.3

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.320C>T; p.P107L; 6:21594854-21594854

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.320C>T; p.P107L; 6:21594854-21594854

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.73G>T; p.G25C; 6:21594607-21594607

 central_nervous_system; braingliomaSubstitution - Missense

c.277C>T; p.L93L; 6:21594811-21594811

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.205T>G; p.W69G; 6:21594739-21594739

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.27G>C; p.E9D; 6:21594561-21594561

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.262G>A; p.E88K; 6:21594796-21594796

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.1157C>T; p.S386F; 6:21595691-21595691

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.82C>G; p.L28V; 6:21594616-21594616

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.812C>T; p.A271V; 6:21595346-21595346

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1203C>T; p.F401F; 6:21595737-21595737

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.1209C>A; p.D403E; 6:21595743-21595743

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.75C>T; p.G25G; 6:21594609-21594609

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.1192_1193GA>TC; p.D398S; 6:21595726-21595727

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.123C>A; p.S41S; 6:21594657-21594657

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.299T>G; p.L100R; 6:21594833-21594833

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.160A>C; p.T54P; 6:21594694-21594694

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.968_969insG; p.L324fs*92; 6:21595502-21595503

 lungcarcinoma; adenocarcinomaInsertion - Frameshift

c.1193A>T; p.D398V; 6:21595727-21595727

 lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.1203C>G; p.F401L; 6:21595737-21595737

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1110C>T; p.A370A; 6:21595644-21595644

 oesophagus; lower_thirdcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.71C>G; p.A24G; 6:21594605-21594605

 pancreascarcinomaSubstitution - Missense

c.187A>G; p.M63V; 6:21594721-21594721

 prostatecarcinomaSubstitution - Missense

c.1253C>T; p.S418F; 6:21595787-21595787

 skinmalignant_melanomaSubstitution - Missense

c.960C>T; p.D320D; 6:21595494-21595494

 skinmalignant_melanomaSubstitution - coding silent

c.331G>A; p.E111K; 6:21594865-21594865

 skinmalignant_melanomaSubstitution - Missense

c.902G>A; p.G301D; 6:21595436-21595436

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.446C>A; p.S149Y; 6:21594980-21594980

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.393G>T; p.R131S; 6:21594927-21594927

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.4G>C; p.V2L; 6:21594538-21594538

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.4G>C; p.V2L; 6:21594538-21594538

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.1376C>G; p.S459W; 6:21595910-21595910

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.1376C>G; p.S459W; 6:21595910-21595910

 urinary_tract; bladdercarcinomaSubstitution - Missense