API

Introduction

The OncoKB™ data can be accessed through a REST API (Swagger Page). The API is defined and organized using swagger annotation. MAF file annotation is also possible by using OncoKB™ Annotator which is fully supported by using OncoKB™ REST APIs.

When you send API requests, you need a token before accessing the OncoKB™ data via its web API. Please visit OncoKB™ Data Access Page for more information about how to register an account and get an OncoKB™ API token.

Authentication

We are using standard Spring Security to protect all our services. In order to access the OncoKB™ data via its REST API, you need to specify your API token in the request header with

Authorization: Bearer [your token]

Your token will be available under your Account Settings after getting a license from the OncoKB™ Team.

OncoKB™ Instances

https://www.oncokb.org

This is the main instance and authenticated. If you have gotten a license from OncoKB™. Please use this instance for most accurate results.

https://demo.oncokb.org

Before committing to our license, you can use this website to test the API and other services freely. We included the full information of BRAF, TP53 and ROS1. The instance is not authenticated.

Annotation API Examples

If you have the access token and like to play around with our endpoints, please see the Swagger page. We only list GET methods here. They all have corresponding POST method available. Please see the Swagger page for more details.

Annotate Mutations by Protein Change

GET https://www.oncokb.org/api/v1/annotate/mutations/byProteinChange

Query Parameters

Headers

{
  "query": {
    "id": null,
    "type": "regular",
    "hugoSymbol": "BRAF",
    "entrezGeneId": 673,
    "alteration": "V600E",
    "alterationType": null,
    "svType": null,
    "tumorType": "Melanoma",
    "consequence": "missense_variant",
    "proteinStart": 600,
    "proteinEnd": 600,
    "hgvs": null
  },
  "geneExist": true,
  "variantExist": true,
  "alleleExist": true,
  "oncogenic": "Predicted Oncogenic",
  "mutationEffect": {
    "knownEffect": "Unknown",
    "description": "",
    "citations": {
      "pmids": [],
      "abstracts": []
    }
  },
  "highestSensitiveLevel": null,
  "highestResistanceLevel": null,
  "highestDiagnosticImplicationLevel": null,
  "highestPrognosticImplicationLevel": null,
  "otherSignificantSensitiveLevels": [],
  "otherSignificantResistanceLevels": [],
  "hotspot": true,
  "geneSummary": "BRAF, an intracellular kinase, is frequently mutated in melanoma, thyroid and lung cancers among others.",
  "variantSummary": "The BRAF V600E mutation is known to be oncogenic.",
  "tumorTypeSummary": "",
  "prognosticSummary": "",
  "diagnosticSummary": "",
  "diagnosticImplications": null,
  "prognosticImplications": null,
  "treatments": [],
  "dataVersion": "v2.1",
  "lastUpdate": "06/04/2018",
  "vus": false
}

Curl Example

www.oncokb

curl -X GET "https://www.oncokb.org/api/v1/annotate/mutations/byProteinChange?hugoSymbol=BRAF&alteration=V600E&tumorType=Melanoma" -H "accept: application/json" -H "Authorization: Bearer [your personal token]"

demo.oncokb

curl -X GET "https://demo.oncokb.org/api/v1/annotate/mutations/byProteinChange?hugoSymbol=BRAF&alteration=V600E&tumorType=Melanom"  -H "accept: application/json"

Typical Use Cases

Missense mutation in an oncogene: BRAF, V600E, Melanoma

https://demo.oncokb.org/api/v1/annotate/mutations/byProteinChange?hugoSymbol=BRAF&alteration=V600E&tumorType=Melanom

Missense mutation in a tumor suppressor: TP53, R273C, Colon Adenocarcinoma

https://demo.oncokb.org/api/v1/annotate/mutations/byProteinChange?hugoSymbol=TP53&alteration=R273C&tumorType=Colon%20Adenocarcinoma

In-frame deletion: BRAF, N486_P490del, Histiocytosis

https://demo.oncokb.org/api/v1/annotate/mutations/byProteinChange?hugoSymbol=BRAF&alteration=N486_P490del&tumorType=Histiocytosis

Fusion: ROS1, CD74-ROS1 fusion, Lung Adenocarcinoma

https://demo.oncokb.org/api/v1/annotate/structuralVariants?hugoSymbolA=CD74&hugoSymbolB=ROS1&structuralVariantType=FUSION&isFunctionalFusion=true&tumorType=Lung%20Adenocarcinoma

Atypical Alterations

For atypical alterations, please also use this endpoint. For instance, but not limited to

  • vII

  • vIII

  • vV

  • CTD or C-terminal domain

  • KDD or Kinase Domain Duplication

  • ITD or Internal Tandem Duplication

  • MSI-H or Microsatellite Instability-High

  • TMB-H or Tumor Mutational Burden-High

Demo site does not have atypical alteration. Please use your authentication token for the following examples

EGFR vIII

curl -X 'GET' \
  'https://www.oncokb.org/api/v1/annotate/mutations/byProteinChange?hugoSymbol=EGFR&alteration=vIII' \
  -H 'accept: application/json' \
  -H 'Authorization: Bearer [your token]'

MSI-H

curl -X 'GET' \
  'https://www.oncokb.org/api/v1/annotate/mutations/byProteinChange?alteration=MSI-H' \
  -H 'accept: application/json' \
  -H 'Authorization: Bearer [your token]'

Annotate Copy Number Alterations

GET https://www.oncokb.org/api/v1/annotate/copyNumberAlterations

Query Parameters

Headers

{
  "query": {
    "id": null,
    "type": "regular",
    "hugoSymbol": "BRAF",
    "entrezGeneId": 673,
    "alteration": "Amplification",
    "alterationType": null,
    "svType": null,
    "tumorType": "melanoma",
    "consequence": null,
    "proteinStart": null,
    "proteinEnd": null,
    "hgvs": null
  },
  "geneExist": true,
  "variantExist": true,
  "alleleExist": false,
  "oncogenic": "Oncogenic",
  "mutationEffect": {
    "knownEffect": "Gain-of-function",
    "description": "",
    "citations": {
      "pmids": [
        "24055054",
        "25618114",
        "22395615",
        "21098728",
        "15467732"
      ],
      "abstracts": []
    }
  },
  "highestSensitiveLevel": null,
  "highestResistanceLevel": null,
  "highestDiagnosticImplicationLevel": null,
  "highestPrognosticImplicationLevel": null,
  "otherSignificantSensitiveLevels": [],
  "otherSignificantResistanceLevels": [],
  "hotspot": false,
  "geneSummary": "BRAF, an intracellular kinase, is frequently mutated in melanoma, thyroid and lung cancers among others.",
  "variantSummary": "BRAF amplification is known to be oncogenic.",
  "tumorTypeSummary": "There are no FDA-approved or NCCN-compendium listed treatments specifically for patients with BRAF-amplified melanoma.",
  "prognosticSummary": "",
  "diagnosticSummary": "",
  "diagnosticImplications": [],
  "prognosticImplications": [],
  "treatments": [],
  "dataVersion": "v2.1",
  "lastUpdate": "07/20/2019",
  "vus": false
}

Curl Example

curl -X GET "https://www.oncokb.org/api/v1/annotate/copyNumberAlterations?hugoSymbol=BRAF&copyNameAlterationType=AMPLIFICATION&tumorType=MEL" -H "accept: application/json" -H "Authorization: Bearer [your personal token]"

Annotate Structural Variants

GET ttps://www.oncokb.org/api/v1/annotate/structuralVariants

Query Parameters

Headers

{
  "query": {
    "id": null,
    "type": "regular",
    "hugoSymbol": "ABL1",
    "entrezGeneId": 25,
    "alteration": "truncating mutation",
    "alterationType": "STRUCTURAL_VARIANT",
    "svType": "DELETION",
    "tumorType": "Melanoma",
    "consequence": "feature_truncation",
    "proteinStart": null,
    "proteinEnd": null,
    "hgvs": null
  },
  "geneExist": true,
  "variantExist": false,
  "alleleExist": false,
  "oncogenic": "",
  "mutationEffect": {
    "knownEffect": "Unknown",
    "description": "",
    "citations": {
      "pmids": [],
      "abstracts": []
    }
  },
  "highestSensitiveLevel": null,
  "highestResistanceLevel": null,
  "highestDiagnosticImplicationLevel": null,
  "highestPrognosticImplicationLevel": null,
  "otherSignificantSensitiveLevels": [],
  "otherSignificantResistanceLevels": [],
  "hotspot": false,
  "geneSummary": "",
  "variantSummary": "",
  "tumorTypeSummary": "",
  "prognosticSummary": "",
  "diagnosticSummary": "",
  "diagnosticImplications": null,
  "prognosticImplications": null,
  "treatments": [],
  "dataVersion": "v2.1",
  "lastUpdate": "02/12/2020",
  "vus": false
}

Curl Example

curl -X GET "https://www.oncokb.org/api/v1/annotate/structuralVariants?hugoSymbolA=ABL1&hugoSymbolB=BCR&structuralVariantType=DELETION&isFunctionalFusion=true&tumorType=Melanoma" -H "accept: application/json" -H "Authorization: Bearer [your personal token]"

Annotate Mutations by Genomic Change

GET https://www.oncokb.org/api/v1/annotate/mutations/byGenomicChange

Query Parameters

Headers

{
  "query": {
    "id": null,
    "type": "regular",
    "hugoSymbol": "BRAF",
    "entrezGeneId": 673,
    "alteration": "V600E",
    "alterationType": null,
    "svType": null,
    "tumorType": "Melanoma",
    "consequence": "missense_variant",
    "proteinStart": 600,
    "proteinEnd": 600,
    "hgvs": null
  },
  "geneExist": true,
  "variantExist": true,
  "alleleExist": true,
  "oncogenic": "Oncogenic",
  "mutationEffect": {
    "knownEffect": "Unknown",
    "description": "",
    "citations": {
      "pmids": [],
      "abstracts": []
    }
  },
  "highestSensitiveLevel": null,
  "highestResistanceLevel": null,
  "highestDiagnosticImplicationLevel": null,
  "highestPrognosticImplicationLevel": null,
  "otherSignificantSensitiveLevels": [],
  "otherSignificantResistanceLevels": [],
  "hotspot": true,
  "geneSummary": "",
  "variantSummary": "",
  "tumorTypeSummary": "",
  "prognosticSummary": "",
  "diagnosticSummary": "",
  "diagnosticImplications": null,
  "prognosticImplications": null,
  "treatments": [],
  "dataVersion": "v2.1",
  "lastUpdate": "04/24/2017",
  "vus": false
}

Curl Example

curl -X GET "https://www.oncokb.org/api/v1/annotate/mutations/byGenomicChange?genomicLocation=7%2C140453136%2C140453136%2CA%2CT&tumorType=Melanoma" -H "accept: application/json" -H "Authorization: Bearer [your personal token]"

Annotate Mutations by HGVSg

GET ttps://www.oncokb.org/api/v1/annotate/mutations/byHGVSg

Query Parameters

Headers

{
  "query": {
    "id": null,
    "type": "regular",
    "hugoSymbol": null,
    "entrezGeneId": null,
    "alteration": "",
    "alterationType": null,
    "svType": null,
    "tumorType": "Melanoma",
    "consequence": null,
    "proteinStart": null,
    "proteinEnd": null,
    "hgvs": "g.140453136A>T"
  },
  "geneExist": false,
  "variantExist": null,
  "alleleExist": null,
  "oncogenic": "",
  "mutationEffect": {
    "knownEffect": "Unknown",
    "description": "",
    "citations": {
      "pmids": [],
      "abstracts": []
    }
  },
  "highestSensitiveLevel": null,
  "highestResistanceLevel": null,
  "highestDiagnosticImplicationLevel": null,
  "highestPrognosticImplicationLevel": null,
  "otherSignificantSensitiveLevels": [],
  "otherSignificantResistanceLevels": [],
  "hotspot": null,
  "geneSummary": "",
  "variantSummary": "",
  "tumorTypeSummary": "",
  "prognosticSummary": "",
  "diagnosticSummary": "",
  "diagnosticImplications": null,
  "prognosticImplications": null,
  "treatments": [],
  "dataVersion": "v2.1",
  "lastUpdate": "02/12/2020",
  "vus": null
}

Curl Example

curl -X GET "https://www.oncokb.org/api/v1/annotate/mutations/byHGVSg?hgvsg=7g.140453136A%3ET&tumorType=Melanoma" -H "accept: application/json" -H "Authorization: Bearer [your personal token]"

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