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Paper Details

ActiveDriverDB: human disease mutations and genome variation in post-translational modification sites of proteins.
Nucleic Acids Res
59
2018
ActiveDriverDB, BRCA2, Cancer, PTM, SNVs, TP53, VHL, amino acid, amino acids, cancer, disease genes, human, human genome, human genomes, inherited disease, kinase-bound sequence motifs, protein sites, single nucleotide variants
Author NameAffiliation
Michal KrassowskiOntario Institute for Cancer Research
Michal KrassowskiUniversity of Warsaw
Marta PaczkowskaOntario Institute for Cancer Research
Kim CullionOntario Institute for Cancer Research
Irakli DzneladzeOntario Institute for Cancer Research
Irakli DzneladzeUniversity of Toronto
Bf Francis OuelletteOntario Institute for Cancer Research
Bf Francis OuelletteUniversity of Toronto
Bf Francis OuelletteOntario Institute for Cancer Research
Bf Francis OuelletteUniversity of Toronto
Joseph T YamadaOntario Institute for Cancer Research
J??ri ReimandOntario Institute for Cancer Research
J??ri ReimandUniversity of Toronto
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Datasets

ActiveDriverDBNo description suppliedLink
ActiveDriverDBNo description suppliedLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link