Gene: CTNNB1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913403
rs121913403
CTNNB1
G 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913403
rs121913403
CTNNB1
T 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913412
rs121913412
CTNNB1
G 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs28931588
rs28931588
CTNNB1
T 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs28931588
rs28931588
CTNNB1
A 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs28931588
rs28931588
CTNNB1
C 0.800 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913228
rs121913228
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs121913396
rs121913396
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs121913399
rs121913399
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs121913400
rs121913400
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs121913403
rs121913403
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs121913412
rs121913412
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs28931588
rs28931588
CTNNB1
0.800 GeneticVariation UNIPROT

dbSNP: rs28931589
rs28931589
CTNNB1
A 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs28931589
rs28931589
CTNNB1
C 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs28931589
rs28931589
CTNNB1
T 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs28931589
rs28931589
CTNNB1
0.710 GeneticVariation BEFREE Only three HCC cases (5.6%) were found mutated at residues (G34E, S45P, P44S, T41I) important for phosphorylation and ubiquitination of beta-catenin protein. 25536643

2015
dbSNP: rs28931589
rs28931589
CTNNB1
A 0.710 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs1057519886
rs1057519886
CTNNB1
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519886
rs1057519886
CTNNB1
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519886
rs1057519886
CTNNB1
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1413975856
rs1413975856
CTNNB1
0.700 GeneticVariation UNIPROT

dbSNP: rs1553631896
rs1553631896
CTNNB1
TA 0.700 CausalMutation CLINVAR

dbSNP: rs775104326
rs775104326
CTNNB1
T 0.700 CausalMutation CLINVAR

dbSNP: rs778624338
rs778624338
CTNNB1
A 0.700 CausalMutation CLINVAR