Pediatric cancer gene database (Pedican) Home
Pedican
Pediatric cancer database
General information | Literature | Expression | Regulation | Variant | Interaction

Basic Information

Gene ID

7132

Name

TNFRSF1A

Synonymous

CD120a|FPF|TBP1|TNF-R|TNF-R-I|TNF-R55|TNFAR|TNFR1|TNFR55|TNFR60|p55|p55-R|p60;tumor necrosis factor receptor superfamily, member 1A;TNFRSF1A;tumor necrosis factor receptor superfamily, member 1A

Definition

TNF-R1|TNF-RI|TNFR-I|tumor necrosis factor binding protein 1|tumor necrosis factor receptor 1A isoform beta|tumor necrosis factor receptor superfamily member 1A|tumor necrosis factor receptor type 1|tumor necrosis factor-alpha receptor

Position

12p13.2

Gene Type

protein-coding

Gene Mutation:

PCGP germline mutation
PCGP somatic mutation
COSMIC somatic mutation

PCGP germline mutation   [Top]

There is no record for TNFRSF1A

PCGP somatic mutation   [Top]

Variant (Variant; Chr; Position)

Genotype (MutationType; MutationClass; ReferenceAllele; Genotype; Origin)

Disease (CancerType; ValidationStatus; SequencingType)

TNFRSF1A_E10_UTR_3; chr12; 6438273

SUB; UTR_3; C; C/T; SOMATICRHB; VALID; WGS

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

c.1026G>T; p.E342D;

large_intestine; coloncarcinoma; adenocarcinoma

c.961G>A; p.A321T;

large_intestine; coloncarcinoma; adenocarcinoma

c.985C>A; p.L329I;

large_intestine; coloncarcinoma; adenocarcinoma

c.237G>A; p.T79T;

lungcarcinoma; adenocarcinoma

c.955C>T; p.Q319*;

lungcarcinoma; squamous_cell_carcinoma

c.1275C>T; p.L425L;

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma

c.734C>T; p.S245F;

haematopoietic_and_lymphoid_tissue; lymph_nodelymphoid_neoplasm; diffuse_large_B_cell_lymphoma

c.625+5G>A; p.?;

stomachcarcinoma; adenocarcinoma

c.740-9T>C; p.?;

stomachcarcinoma; adenocarcinoma

c.236C>T; p.T79M;

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinoma

c.955C>T; p.Q319*;

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinoma

c.760G>A; p.E254K; 12:6309702-6309702

skinmalignant_melanoma

c.842_843insT; p.T282fs*22;

autonomic_ganglianeuroblastoma

c.147T>C; p.Y49Y;

bonechondrosarcoma

c.432C>G; p.F144L;

ovarycarcinoma; serous_carcinoma

c.1368A>T; p.*456C;

ovarycarcinoma; serous_carcinoma

c.1070C>T; p.A357V;

lungcarcinoma; squamous_cell_carcinoma

c.567G>T; p.L189L;

lungcarcinoma; squamous_cell_carcinoma

c.619G>A; p.D207N;

lungcarcinoma; squamous_cell_carcinoma

c.36A>G; p.P12P;

breastcarcinoma

c.531C>T; p.N177N;

large_intestine; coloncarcinoma; adenocarcinoma

c.47T>C; p.L16P;

large_intestine; caecumcarcinoma; adenocarcinoma

c.167C>T; p.S56L;

endometriumcarcinoma; endometrioid_carcinoma

c.457A>G; p.T153A;

endometriumcarcinoma; endometrioid_carcinoma

c.213C>T; p.D71D;

endometriumcarcinoma; endometrioid_carcinoma

c.167C>T; p.S56L;

large_intestine; caecumcarcinoma; adenocarcinoma

c.46C>T; p.L16L;

kidneycarcinoma; clear_cell_renal_cell_carcinoma

c.841C>A; p.P281T;

endometriumcarcinoma; endometrioid_carcinoma

c.212A>G; p.D71G;

endometriumcarcinoma; endometrioid_carcinoma

c.362G>A; p.R121Q;

breastcarcinoma

c.623C>T; p.S208L;

kidneycarcinoma; clear_cell_renal_cell_carcinoma

c.168G>A; p.S56S;

endometriumcarcinoma; endometrioid_carcinoma

c.74C>T; p.S25L;

breastcarcinoma

c.106G>T; p.D36Y;

kidneycarcinoma; clear_cell_renal_cell_carcinoma

c.681C>A; p.L227L;

kidneycarcinoma; clear_cell_renal_cell_carcinoma

c.526G>T; p.E176*;

endometriumcarcinoma; endometrioid_carcinoma

c.79delG; p.V27fs*8;

large_intestine; coloncarcinoma; adenocarcinoma

c.68A>G; p.Y23C;

large_intestine; coloncarcinoma; adenocarcinoma

c.217C>T; p.P73S;

skinmalignant_melanoma


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