Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519992
rs1057519992
TP53
C 0.700 GeneticVariation CLINVAR Altered-function p53 missense mutations identified in breast cancers can have subtle effects on transactivation. 20407015

2010
dbSNP: rs1057519992
rs1057519992
TP53
C 0.700 GeneticVariation CLINVAR TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes. 20522432

2010
dbSNP: rs1057519992
rs1057519992
TP53
C 0.700 GeneticVariation CLINVAR Complex functions of mutant p53 alleles from human prostate cancer. 11920959

2002
dbSNP: rs1057519992
rs1057519992
TP53
C 0.700 GeneticVariation CLINVAR p53 status in multiple human urothelial cancers: assessment for clonality by the yeast p53 functional assay in combination with p53 immunohistochemistry. 10761705

2000
dbSNP: rs1057519992
rs1057519992
TP53
C 0.700 GeneticVariation CLINVAR Identification of human p53 mutations with differential effects on the bax and p21 promoters using functional assays in yeast. 9546439

1998
dbSNP: rs1057519992
rs1057519992
TP53
C 0.700 GeneticVariation CLINVAR Screening the p53 status of human cell lines using a yeast functional assay. 9290701

1997
dbSNP: rs1057519992
rs1057519992
TP53
C 0.700 GeneticVariation CLINVAR A simple p53 functional assay for screening cell lines, blood, and tumors. 7732013

1995