Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
0.820 | GeneticVariation | UNIPROT | |||||||
|
T | 0.820 | CausalMutation | CLINVAR | ||||||
|
0.810 | GeneticVariation | UNIPROT | |||||||
|
C | 0.810 | CausalMutation | CLINVAR | ||||||
|
0.810 | GeneticVariation | UNIPROT | |||||||
|
0.800 | GeneticVariation | UNIPROT | |||||||
|
0.800 | GeneticVariation | UNIPROT | |||||||
|
0.800 | GeneticVariation | UNIPROT | |||||||
|
0.800 | GeneticVariation | UNIPROT | |||||||
|
0.800 | GeneticVariation | UNIPROT | |||||||
|
0.800 | GeneticVariation | UNIPROT | |||||||
|
0.800 | GeneticVariation | UNIPROT | |||||||
|
0.700 | GeneticVariation | UNIPROT | |||||||
|
TA | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.710 | GeneticVariation | CLINVAR | Prospective enterprise-level molecular genotyping of a cohort of cancer patients. | 25157968 | 2014 |
|||
|
0.810 | 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 |
||||
|
0.810 | 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 |
||||
|
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 |
||||
|
G | 0.820 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 |
|||
|
T | 0.820 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 |
|||
|
A | 0.820 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 |
|||
|
C | 0.810 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 |
|||
|
A | 0.810 | GeneticVariation | CLINVAR | Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. | 26619011 | 2016 |