{
  "data": [
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      "@id": "https://erepo.genome.network/evrepo/api/summary/classification/c4aa1004-6cff-4317-b302-93c0aeff6eea/doc/sepio/version/1.0.0",
      "assertionMethod": {
        "@id": "https://cspec.genome.network/cspec/SequenceVariantInterpretation/id/1576926543",
        "label": "ClinGen Hereditary Hemorrhagic Telangiectasia Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for ENG Version 1.1.0",
        "type": "VariantPathogenicityInterpretationGuideline",
        "version": "1.1.0"
      },
      "condition": {
        "@id": "https://api.monarchinitiative.org/api/bioentity/phenotype/MONDO:0008535",
        "id": "MONDO:0008535",
        "label": "telangiectasia, hereditary hemorrhagic, type 1",
        "type": "GeneticCondition"
      },
      "evidenceLine": [
        {
          "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/el/0/1765",
          "evidenceItem": [
            {
              "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/ei/1/1766",
              "contribution": [
                {
                  "agent": {
                    "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50037_EP171050563120248",
                    "id": "CG-PCER-AGENT:CG_50037_EP171050563120248",
                    "type": "Agent"
                  },
                  "contributionDate": {
                    "date": "2025/3/25",
                    "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"
                }
              ],
              "evidenceLine": [
                {
                  "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/el/0/1765/1767",
                  "evidenceItem": [
                    {
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                            "id": "CG-PCER-AGENT:CG_50037_EP171050563120248",
                            "type": "Agent"
                          },
                          "comments": "Another missense variant, c.1517T>C, p.Leu506Pro (PMID: 24196379, 30073140; ClinVar Variation ID: 1774348), in the same codon has been classified as likely pathogenic for autosomal dominant Hereditary Hemorrhagic Telangiectasia by the ClinGen Hereditary Hemorrhagic Telangiectasia Variant Curation Expert Panel (PM5).",
                          "contributionDate": {
                            "date": "2025/3/25",
                            "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": "CA5252743/MONDO:0008535/136/ci/CA5252743/MONDO:0008535/136.002",
                      "type": "InfFromBkgrndSciKnow"
                    }
                  ],
                  "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/0/1765/1767",
                  "type": "EvidenceLine"
                }
              ],
              "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/1/1766",
              "statementOutcome": {
                "@id": "SEPIO:0000224",
                "label": "Met"
              },
              "type": "CriterionAssessment"
            }
          ],
          "evidenceStrength": {
            "@id": "https://obofoundry.org/sepio"
          },
          "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/0/1765",
          "type": "EvidenceLine"
        },
        {
          "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/el/0/1699",
          "evidenceItem": [
            {
              "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/ei/1/1700",
              "contribution": [
                {
                  "agent": {
                    "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50037_EP171050563120248",
                    "id": "CG-PCER-AGENT:CG_50037_EP171050563120248",
                    "type": "Agent"
                  },
                  "contributionDate": {
                    "date": "2025/3/25",
                    "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"
                }
              ],
              "evidenceLine": [
                {
                  "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/el/0/1699/1701",
                  "evidenceItem": [
                    {
                      "@id": "CG-PCER:curatorInference/CA5252743/MONDO:0008535/136/ci/CA5252743/MONDO:0008535/136.002",
                      "contribution": [
                        {
                          "agent": {
                            "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50037_EP171050563120248",
                            "id": "CG-PCER-AGENT:CG_50037_EP171050563120248",
                            "type": "Agent"
                          },
                          "comments": "This variant has been reported in 2 probands with a phenotype consistent with HHT (PS4_Moderate; Internal lab contributors).",
                          "contributionDate": {
                            "date": "2025/3/25",
                            "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": "CA5252743/MONDO:0008535/136/ci/CA5252743/MONDO:0008535/136.002",
                      "type": "InfFromBkgrndSciKnow"
                    }
                  ],
                  "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/0/1699/1701",
                  "type": "EvidenceLine"
                }
              ],
              "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/1/1700",
              "statementOutcome": {
                "@id": "SEPIO:0000224",
                "label": "Met"
              },
              "type": "CriterionAssessment"
            }
          ],
          "evidenceStrength": {
            "@id": "https://obofoundry.org/sepio"
          },
          "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/0/1699",
          "type": "EvidenceLine"
        },
        {
          "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/el/0/1747",
          "evidenceItem": [
            {
              "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/ei/1/1748",
              "contribution": [
                {
                  "agent": {
                    "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50037_EP171050563120248",
                    "id": "CG-PCER-AGENT:CG_50037_EP171050563120248",
                    "type": "Agent"
                  },
                  "contributionDate": {
                    "date": "2025/3/25",
                    "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"
                }
              ],
              "evidenceLine": [
                {
                  "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/el/0/1747/1749",
                  "evidenceItem": [
                    {
                      "@id": "CG-PCER:curatorInference/CA5252743/MONDO:0008535/136/ci/CA5252743/MONDO:0008535/136.002",
                      "contribution": [
                        {
                          "agent": {
                            "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50037_EP171050563120248",
                            "id": "CG-PCER-AGENT:CG_50037_EP171050563120248",
                            "type": "Agent"
                          },
                          "comments": "The computational predictor REVEL gives a score of 0.88, which is above the threshold of ≥0.644, evidence that correlates with impact to ENG function (PP3).",
                          "contributionDate": {
                            "date": "2025/3/25",
                            "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": "CA5252743/MONDO:0008535/136/ci/CA5252743/MONDO:0008535/136.002",
                      "type": "InfFromBkgrndSciKnow"
                    }
                  ],
                  "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/0/1747/1749",
                  "type": "EvidenceLine"
                }
              ],
              "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/1/1748",
              "statementOutcome": {
                "@id": "SEPIO:0000224",
                "label": "Met"
              },
              "type": "CriterionAssessment"
            }
          ],
          "evidenceStrength": {
            "@id": "https://obofoundry.org/sepio"
          },
          "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/0/1747",
          "type": "EvidenceLine"
        },
        {
          "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/el/0/1636",
          "evidenceItem": [
            {
              "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/ei/1/1637",
              "contribution": [
                {
                  "agent": {
                    "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50037_EP171050563120248",
                    "id": "CG-PCER-AGENT:CG_50037_EP171050563120248",
                    "type": "Agent"
                  },
                  "contributionDate": {
                    "date": "2025/3/25",
                    "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"
                }
              ],
              "evidenceLine": [
                {
                  "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA5252743/MONDO:0008535/136/el/0/1636/1638",
                  "evidenceItem": [
                    {
                      "@id": "CG-PCER:curatorInference/CA5252743/MONDO:0008535/136/ci/CA5252743/MONDO:0008535/136.002",
                      "contribution": [
                        {
                          "agent": {
                            "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50037_EP171050563120248",
                            "id": "CG-PCER-AGENT:CG_50037_EP171050563120248",
                            "type": "Agent"
                          },
                          "comments": "The overall minor allele frequency in gnomAD v2.1.1 is 0.000004 (1/250772 alleles), which is lower than the ClinGen Hereditary Hemorrhagic Telangiectasia VCEP threshold (<6 total alleles) for PM2_Supporting, meeting this criterion (PM2_Supporting). ",
                          "contributionDate": {
                            "date": "2025/3/25",
                            "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": "CA5252743/MONDO:0008535/136/ci/CA5252743/MONDO:0008535/136.002",
                      "type": "InfFromBkgrndSciKnow"
                    }
                  ],
                  "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/0/1636/1638",
                  "type": "EvidenceLine"
                }
              ],
              "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/1/1637",
              "statementOutcome": {
                "@id": "SEPIO:0000224",
                "label": "Met"
              },
              "type": "CriterionAssessment"
            }
          ],
          "evidenceStrength": {
            "@id": "https://obofoundry.org/sepio"
          },
          "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136/0/1636",
          "type": "EvidenceLine"
        }
      ],
      "id": "CG-PCER-VARINT:CA5252743/MONDO:0008535/136",
      "metadata": {
        "created": "2025-04-01T16:27:34.325Z",
        "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": "Tue, 01 Apr 2025 16:27:34 -0000",
        "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
        "version": "1.0.0"
      },
      "statementOutcome": {
        "@id": "https://loinc.org/LA26332-9",
        "id": "LN:LA26332-9",
        "label": "Likely Pathogenic"
      },
      "type": "VariantPathogenicityInterpretation",
      "uuid": "c4aa1004-6cff-4317-b302-93c0aeff6eea",
      "variant": {
        "@id": "https://reg.genome.network/allele/CA5252743",
        "id": "CAR:CA5252743",
        "relatedContextualAllele": [
          {
            "alleleName": [
              {
                "name": "NM_001114753.3:c.1517T>A"
              }
            ],
            "preferred": true
          }
        ],
        "relatedIdentifier": [
          {
            "label": "NM_001114753.3(ENG):c.1517T>A (p.Leu506His)"
          }
        ],
        "type": "CAR"
      }
    }
  ],
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-04-05T07:12:36.827Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}