{
  "data": {
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    "@id": "https://erepo.genome.network/evrepo/api/summary/classification/318690ae-2743-4195-8d9b-e2e84ff94494/doc/sepio/version/1.0.0",
    "assertionMethod": {
      "@id": "https://cspec.genome.network/cspec/SequenceVariantInterpretation/id/1527855755",
      "label": "ClinGen VHL Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for VHL Version 1.0.0",
      "type": "VariantPathogenicityInterpretationGuideline",
      "version": "1.0.0"
    },
    "condition": {
      "@id": "https://api.monarchinitiative.org/api/bioentity/phenotype/MONDO:0008667",
      "id": "MONDO:0008667",
      "label": "von Hippel-Lindau disease",
      "type": "GeneticCondition"
    },
    "evidenceLine": [
      {
        "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA020186/MONDO:0008667/078/el/0/1648",
        "evidenceItem": [
          {
            "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA020186/MONDO:0008667/078/ei/1/1649",
            "contribution": [
              {
                "agent": {
                  "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50036_EP171933178180385",
                  "id": "CG-PCER-AGENT:CG_50036_EP171933178180385",
                  "type": "Agent"
                },
                "contributionDate": {
                  "date": "2024/6/25",
                  "description": "Date on which this evidence was provided"
                },
                "contributionRole": {
                  "@id": "https://obofoundry.org/sepio/0000156",
                  "id": "SEPIO:0000516",
                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
              }
            ],
            "criterion": {
              "@id": "https://obofoundry.org/sepio/clingen/0023",
              "defaultStrength": {
                "@id": "https://obofoundry.org/sepio/SEPIO:0000330",
                "id": "SEPIO:0000330",
                "label": "Pathogenic Strong"
              },
              "id": "0023",
              "label": "PP1",
              "type": "Criterion"
            },
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA020186/MONDO:0008667/078/el/0/1648/1650",
                "evidenceItem": [
                  {
                    "@id": "CG-PCER:curatorInference/CA020186/MONDO:0008667/078/ci/CA020186/MONDO:0008667/078.002",
                    "contribution": [
                      {
                        "agent": {
                          "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50036_EP171933178180385",
                          "id": "CG-PCER-AGENT:CG_50036_EP171933178180385",
                          "type": "Agent"
                        },
                        "comments": "Two unrelated VHL families with a total of 12 affected individuals with this VHL variant. Detailed relationship not provided but this would meet \">7 meioses across >=2 families\" criteria for PP1_Strong.",
                        "contributionDate": {
                          "date": "2024/6/25",
                          "description": "Date on which this evidence was provided"
                        },
                        "contributionRole": {
                          "@id": "https://obofoundry.org/sepio/0000156",
                          "id": "SEPIO:0000516",
                          "label": "curator role",
                          "type": "ContributoryRole"
                        },
                        "type": "Contribution"
                      }
                    ],
                    "id": "CA020186/MONDO:0008667/078/ci/CA020186/MONDO:0008667/078.002",
                    "type": "InfFromBkgrndSciKnow"
                  }
                ],
                "id": "CG-PCER-VARINT:CA020186/MONDO:0008667/078/0/1648/1650",
                "type": "EvidenceLine"
              }
            ],
            "id": "CG-PCER-VARINT:CA020186/MONDO:0008667/078/1/1649",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA020186/MONDO:0008667/078/0/1648",
        "type": "EvidenceLine"
      },
      {
        "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA020186/MONDO:0008667/078/el/0/1636",
        "evidenceItem": [
          {
            "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA020186/MONDO:0008667/078/ei/1/1637",
            "contribution": [
              {
                "agent": {
                  "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50036_EP171933178180385",
                  "id": "CG-PCER-AGENT:CG_50036_EP171933178180385",
                  "type": "Agent"
                },
                "contributionDate": {
                  "date": "2024/6/25",
                  "description": "Date on which this evidence was provided"
                },
                "contributionRole": {
                  "@id": "https://obofoundry.org/sepio/0000156",
                  "id": "SEPIO:0000516",
                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
              }
            ],
            "criterion": {
              "@id": "https://obofoundry.org/sepio/clingen/0030",
              "defaultStrength": {
                "@id": "https://obofoundry.org/sepio/SEPIO:0000329",
                "id": "SEPIO:0000329",
                "label": "Pathogenic Supporting"
              },
              "id": "0030",
              "label": "PM2",
              "type": "Criterion"
            },
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA020186/MONDO:0008667/078/el/0/1636/1638",
                "evidenceItem": [
                  {
                    "@id": "CG-PCER:curatorInference/CA020186/MONDO:0008667/078/ci/CA020186/MONDO:0008667/078.002",
                    "contribution": [
                      {
                        "agent": {
                          "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50036_EP171933178180385",
                          "id": "CG-PCER-AGENT:CG_50036_EP171933178180385",
                          "type": "Agent"
                        },
                        "comments": "This variant is absent from gnomAD v4.1.0 (PM2_Supporting). ",
                        "contributionDate": {
                          "date": "2024/6/25",
                          "description": "Date on which this evidence was provided"
                        },
                        "contributionRole": {
                          "@id": "https://obofoundry.org/sepio/0000156",
                          "id": "SEPIO:0000516",
                          "label": "curator role",
                          "type": "ContributoryRole"
                        },
                        "type": "Contribution"
                      }
                    ],
                    "id": "CA020186/MONDO:0008667/078/ci/CA020186/MONDO:0008667/078.002",
                    "type": "InfFromBkgrndSciKnow"
                  }
                ],
                "id": "CG-PCER-VARINT:CA020186/MONDO:0008667/078/0/1636/1638",
                "type": "EvidenceLine"
              }
            ],
            "id": "CG-PCER-VARINT:CA020186/MONDO:0008667/078/1/1637",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA020186/MONDO:0008667/078/0/1636",
        "type": "EvidenceLine"
      },
      {
        "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA020186/MONDO:0008667/078/el/0/1735",
        "evidenceItem": [
          {
            "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA020186/MONDO:0008667/078/ei/1/1736",
            "contribution": [
              {
                "agent": {
                  "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50036_EP171933178180385",
                  "id": "CG-PCER-AGENT:CG_50036_EP171933178180385",
                  "type": "Agent"
                },
                "contributionDate": {
                  "date": "2024/6/25",
                  "description": "Date on which this evidence was provided"
                },
                "contributionRole": {
                  "@id": "https://obofoundry.org/sepio/0000156",
                  "id": "SEPIO:0000516",
                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
              }
            ],
            "criterion": {
              "@id": "https://obofoundry.org/sepio/clingen/0053",
              "defaultStrength": {
                "@id": "https://obofoundry.org/sepio/SEPIO:0000330",
                "id": "SEPIO:0000330",
                "label": "Pathogenic Strong"
              },
              "id": "0053",
              "label": "PS4",
              "type": "Criterion"
            },
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA020186/MONDO:0008667/078/el/0/1735/1737",
                "evidenceItem": [
                  {
                    "@id": "CG-PCER:curatorInference/CA020186/MONDO:0008667/078/ci/CA020186/MONDO:0008667/078.002",
                    "contribution": [
                      {
                        "agent": {
                          "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50036_EP171933178180385",
                          "id": "CG-PCER-AGENT:CG_50036_EP171933178180385",
                          "type": "Agent"
                        },
                        "comments": "At least 10 probands either meeting Danish criteria (1 point each) or minor features of VHL (0.5 points for consistent with VHL phenotype, and 0.25 points for nonspecific features). Total proband points reached is 7.5 (5-15 points = PS4)",
                        "contributionDate": {
                          "date": "2024/6/25",
                          "description": "Date on which this evidence was provided"
                        },
                        "contributionRole": {
                          "@id": "https://obofoundry.org/sepio/0000156",
                          "id": "SEPIO:0000516",
                          "label": "curator role",
                          "type": "ContributoryRole"
                        },
                        "type": "Contribution"
                      }
                    ],
                    "id": "CA020186/MONDO:0008667/078/ci/CA020186/MONDO:0008667/078.002",
                    "type": "InfFromBkgrndSciKnow"
                  }
                ],
                "id": "CG-PCER-VARINT:CA020186/MONDO:0008667/078/0/1735/1737",
                "type": "EvidenceLine"
              }
            ],
            "id": "CG-PCER-VARINT:CA020186/MONDO:0008667/078/1/1736",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA020186/MONDO:0008667/078/0/1735",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA020186/MONDO:0008667/078",
    "metadata": {
      "created": "2024-09-28T04:54:24.751Z",
      "note": "DISCLAIMER: While the data/content in this document is approved by ClinGen expert panel(s), the SEPIO schema presented here is an initial prototype and has not been reviewed nor finalized by the ClinGen Data Exchange Modeling Team. We expect it to differ significantly from the final schema.",
      "producedAtUTC": "Sat, 28 Sep 2024 04:54:24 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "1.0.0"
    },
    "statementOutcome": {
      "@id": "https://loinc.org/LA6668-3",
      "id": "LN:LA6668-3",
      "label": "Pathogenic"
    },
    "type": "VariantPathogenicityInterpretation",
    "uuid": "318690ae-2743-4195-8d9b-e2e84ff94494",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA020186",
      "id": "CAR:CA020186",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_000551.4:c.257C>T"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_000551.4(VHL):c.257C>T (p.Pro86Leu)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-03-15T23:48:09.786Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}