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Pediatric cancer database
General information | Literature | Expression | Regulation | Variant | Interaction

Basic Information

Gene ID

8792

Name

TNFRSF11A

Synonymous

CD265|FEO|LOH18CR1|ODFR|OFE|OPTB7|OSTS|PDB2|RANK|TRANCER;tumor necrosis factor receptor superfamily, member 11a, NFKB activator;TNFRSF11A;tumor necrosis factor receptor superfamily, member 11a, NFKB activator

Definition

loss of heterozygosity, 18, chromosomal region 1|osteoclast differentiation factor receptor|receptor activator of NF-KB|receptor activator of nuclear factor-kappa B|tumor necrosis factor receptor superfamily member 11A|tumor necrosis factor receptor super

Position

18q22.1

Gene Type

protein-coding

Gene Mutation:

PCGP germline mutation
PCGP somatic mutation
COSMIC somatic mutation

PCGP germline mutation   [Top]

There is no record for TNFRSF11A

PCGP somatic mutation   [Top]

There is no record for TNFRSF11A

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

c.1193G>T; p.G398V;

livercarcinoma; hepatocellular_carcinoma

c.721G>A; p.A241T;

breastcarcinoma; HER-positive_carcinoma

c.1048A>C; p.M350L;

lungcarcinoma; adenocarcinoma

c.547G>C; p.E183Q;

lungcarcinoma; small_cell_carcinoma

c.1246A>G; p.M416V;

large_intestine; coloncarcinoma; adenocarcinoma

c.214G>T; p.G72C;

large_intestine; coloncarcinoma; adenocarcinoma

c.783+1G>A; p.?;

large_intestine; coloncarcinoma; adenocarcinoma

c.517A>G; p.T173A;

breastcarcinoma; ER-PR-positive_carcinoma

c.405G>A; p.P135P;

oesophaguscarcinoma; adenocarcinoma

c.233A>T; p.D78V;

upper_aerodigestive_tract; larynxcarcinoma; squamous_cell_carcinoma

c.1535G>A; p.G512E;

skin; head_neckmalignant_melanoma; superficial_spreading

c.1349G>A; p.R450Q;

lungcarcinoma; adenocarcinoma

c.577G>T; p.V193F;

lungcarcinoma; adenocarcinoma

c.964G>A; p.E322K;

central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastoma

c.1417G>A; p.A473T;

NSNS

c.1675G>T; p.A559S;

lungcarcinoma; small_cell_carcinoma

c.907G>T; p.D303Y;

breastcarcinoma

c.84G>A; p.L28L;

prostateadenoma

c.662C>T; p.A221V;

autonomic_ganglianeuroblastoma

c.337G>T; p.A113S;

lungcarcinoma; squamous_cell_carcinoma

c.220G>A; p.D74N;

ovarycarcinoma; serous_carcinoma

c.661G>A; p.A221T;

lungcarcinoma; squamous_cell_carcinoma

c.101G>A; p.C34Y;

lungcarcinoma; adenocarcinoma

c.1518G>T; p.R506S;

lung; right_upper_lobecarcinoma; adenocarcinoma

c.1239G>T; p.W413C;

lungcarcinoma; adenocarcinoma

c.1441G>A; p.E481K;

lungcarcinoma; adenocarcinoma

c.491C>T; p.S164F;

ovarycarcinoma; serous_carcinoma

c.756G>A; p.E252E;

large_intestine; caecumcarcinoma; adenocarcinoma

c.559A>G; p.T187A;

large_intestine; coloncarcinoma; adenocarcinoma

c.545T>C; p.V182A;

large_intestine; caecumcarcinoma; adenocarcinoma

c.214G>A; p.G72S;

breastcarcinoma

c.741G>A; p.W247*;

large_intestine; coloncarcinoma; adenocarcinoma

c.820G>A; p.A274T;

large_intestine; caecumcarcinoma; adenocarcinoma

c.132A>G; p.G44G;

large_intestine; rectumcarcinoma; adenocarcinoma

c.173C>A; p.S58Y;

large_intestine; rectumcarcinoma; adenocarcinoma

c.955G>A; p.A319T;

breastcarcinoma

c.1359T>C; p.P453P;

endometriumcarcinoma; endometrioid_carcinoma

c.1568G>T; p.G523V;

endometriumcarcinoma; endometrioid_carcinoma

c.1365G>T; p.E455D;

endometriumcarcinoma; endometrioid_carcinoma

c.421C>T; p.H141Y;

breastcarcinoma

c.219G>A; p.P73P;

cervixcarcinoma; squamous_cell_carcinoma

c.1568G>T; p.G523V;

endometriumcarcinoma; endometrioid_carcinoma

c.301G>A; p.V101M;

large_intestine; coloncarcinoma; adenocarcinoma

c.1702C>T; p.R568C;

endometriumcarcinoma; endometrioid_carcinoma

c.1115C>A; p.P372H;

endometriumcarcinoma; endometrioid_carcinoma

c.1584C>T; p.N528N;

large_intestine; caecumcarcinoma; adenocarcinoma

c.1293C>A; p.C431*;

skin; neckmalignant_melanoma

c.1295C>T; p.P432L;

skin; neckmalignant_melanoma

c.424C>T; p.P142S;

skin; facecarcinoma; squamous_cell_carcinoma

c.1556C>T; p.S519F;

skin; scalpcarcinoma; squamous_cell_carcinoma

c.584G>A; p.S195N;

kidneycarcinoma; clear_cell_renal_cell_carcinoma


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