Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 324
Gene Symbol: APC
APC 		0.110 CausalMutation group CLINVAR Screening for germ-line mutations in familial adenomatous polyposis patients: 61 new patients and a summary of 150 unrelated patients. 1338764 1992
Entrez Id: 5925
Gene Symbol: RB1
RB1 		0.100 CausalMutation group CLINVAR Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype. 1352883 1992
Entrez Id: 5979
Gene Symbol: RET
RET 		0.200 GeneticVariation group BEFREE Prediction of affected MEN2A gene carriers by DNA linkage analysis for early total thyroidectomy: a progress in clinical screening program for children with hereditary cancer syndrome. 1355790 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 GeneticVariation group CLINVAR TP53 tumor suppressor gene: a model for investigating human mutagenesis. 1377002 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 CausalMutation group CLINVAR Germ-line splicing mutation of the p53 gene in a cancer-prone family. 1467311 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 GeneticVariation group CLINVAR Constitutional p53 mutation in a non-Li-Fraumeni cancer family. 1562462 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 CausalMutation group CLINVAR Prevalence and spectrum of germline mutations of the p53 gene among patients with sarcoma. 1565143 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 GeneticVariation group CLINVAR Prevalence and spectrum of germline mutations of the p53 gene among patients with sarcoma. 1565143 1992
Entrez Id: 5925
Gene Symbol: RB1
RB1 		0.100 CausalMutation group CLINVAR Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresis. 1577465 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 GeneticVariation group CLINVAR Inherited p53 gene mutations in breast cancer. 1581912 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 GeneticVariation group CLINVAR Screening for germ line TP53 mutations in breast cancer patients. 1591732 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 CausalMutation group CLINVAR Screening for germ line TP53 mutations in breast cancer patients. 1591732 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 GeneticVariation group CLINVAR Germ-line mutations of the p53 tumor suppressor gene in patients with high risk for cancer inactivate the p53 protein. 1631137 1992
Entrez Id: 324
Gene Symbol: APC
APC 		0.110 CausalMutation group CLINVAR Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. 1651563 1991
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 GeneticVariation group CLINVAR TP53 gene mutations and 17p deletions in human astrocytomas. 1686725 1991
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 GeneticVariation group CLINVAR Hereditary and acquired p53 gene mutations in childhood acute lymphoblastic leukemia. 1737852 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 CausalMutation group CLINVAR A germ line mutation in exon 5 of the p53 gene in an extended cancer family. 1933902 1991
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 CausalMutation group CLINVAR Inactivation of the p53 gene expression by a splice donor site mutation in a human T-cell leukemia cell line. 1961027 1991
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 CausalMutation group CLINVAR Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. 1978757 1990
Entrez Id: 4763
Gene Symbol: NF1
NF1 		0.100 CausalMutation group CLINVAR A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations. 2114220 1990
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.130 GeneticVariation group CLINVAR Misdiagnosis of the Zollinger-Ellison syndrome due to hyperlipidemia. 2210261 1990
Entrez Id: 7157
Gene Symbol: TP53
TP53 		0.170 CausalMutation group CLINVAR Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome. 2259385 1991
Entrez Id: 4286
Gene Symbol: MITF
MITF 		0.100 CausalMutation group CLINVAR Conformation of cytoplasmic segments of acetylcholine receptor alpha- and beta-subunits probed by monoclonal antibodies: sensitivity of the antibody competition approach. 2440678 1987
Entrez Id: 472
Gene Symbol: ATM
ATM 		0.100 CausalMutation group CLINVAR ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome. 2491181 1989
Entrez Id: 5925
Gene Symbol: RB1
RB1 		0.100 CausalMutation group CLINVAR Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling. 2594029 1989