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      "label": "ClinGen Severe Combined Immunodeficiency Disease  Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for IL2RG Version 1.0.0",
      "type": "VariantPathogenicityInterpretationGuideline",
      "version": "1.0.0"
    },
    "condition": {
      "@id": "https://api.monarchinitiative.org/api/bioentity/phenotype/MONDO:0010315",
      "id": "MONDO:0010315",
      "label": "T-B+ severe combined immunodeficiency due to gamma chain deficiency",
      "type": "GeneticCondition"
    },
    "evidenceLine": [
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                },
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                },
                "contributionRole": {
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                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
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            ],
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              "@id": "https://obofoundry.org/sepio/clingen/0017",
              "defaultStrength": {
                "@id": "https://obofoundry.org/sepio/SEPIO:0000220",
                "id": "SEPIO:0000220",
                "label": "Pathogenic Very Strong"
              },
              "id": "0017",
              "label": "PVS1",
              "type": "Criterion"
            },
            "evidenceLine": [
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                "@id": "https://genboree.org/evrepo/api/interpretation/CA413496915/MONDO:0010315/129/el/0/1594/1596",
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                        },
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                          "date": "2024/6/12",
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                      }
                    ],
                    "id": "CA413496915/MONDO:0010315/129/ci/CA413496915/MONDO:0010315/129.002",
                    "type": "InfFromBkgrndSciKnow"
                  }
                ],
                "id": "CG-PCER-VARINT:CA413496915/MONDO:0010315/129/0/1594/1596",
                "type": "EvidenceLine"
              }
            ],
            "id": "CG-PCER-VARINT:CA413496915/MONDO:0010315/129/1/1595",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA413496915/MONDO:0010315/129/0/1594",
        "type": "EvidenceLine"
      },
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        "evidenceItem": [
          {
            "@id": "https://genboree.org/evrepo/api/interpretation/CA413496915/MONDO:0010315/129/ei/1/1637",
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                "contributionDate": {
                  "date": "2024/6/12",
                  "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://genboree.org/evrepo/api/interpretation/CA413496915/MONDO:0010315/129/el/0/1636/1638",
                "evidenceItem": [
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                          "type": "Agent"
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                        "comments": "The variant is absent in gnomAD v4 (PM2_supporting). ",
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                          "description": "Date on which this evidence was provided"
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                    ],
                    "id": "CA413496915/MONDO:0010315/129/ci/CA413496915/MONDO:0010315/129.002",
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                ],
                "id": "CG-PCER-VARINT:CA413496915/MONDO:0010315/129/0/1636/1638",
                "type": "EvidenceLine"
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            ],
            "id": "CG-PCER-VARINT:CA413496915/MONDO:0010315/129/1/1637",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA413496915/MONDO:0010315/129/0/1636",
        "type": "EvidenceLine"
      },
      {
        "@id": "https://genboree.org/evrepo/api/interpretation/CA413496915/MONDO:0010315/129/el/0/1633",
        "evidenceItem": [
          {
            "@id": "https://genboree.org/evrepo/api/interpretation/CA413496915/MONDO:0010315/129/ei/1/1634",
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              {
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                  "@id": "https://genboree.org/evrepo/api//agent/CG_50091_EP170474609917003",
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                },
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                  "date": "2024/6/12",
                  "description": "Date on which this evidence was provided"
                },
                "contributionRole": {
                  "@id": "https://obofoundry.org/sepio/0000156",
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                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
              }
            ],
            "criterion": {
              "@id": "https://obofoundry.org/sepio/clingen/0063",
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                "@id": "https://obofoundry.org/sepio/SEPIO:0000329",
                "id": "SEPIO:0000329",
                "label": "Pathogenic Supporting"
              },
              "id": "0063",
              "label": "PP4",
              "type": "Criterion"
            },
            "evidenceLine": [
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                        },
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                          "description": "Date on which this evidence was provided"
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                        },
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                      }
                    ],
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                  }
                ],
                "id": "CG-PCER-VARINT:CA413496915/MONDO:0010315/129/0/1633/1635",
                "type": "EvidenceLine"
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            ],
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              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA413496915/MONDO:0010315/129/0/1633",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA413496915/MONDO:0010315/129",
    "metadata": {
      "created": "2024-09-23T22:25:31.160Z",
      "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": "Mon, 23 Sep 2024 22:25:31 -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": "c4092af2-9815-4b28-8afb-597deb955bd3",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA413496915",
      "id": "CAR:CA413496915",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_000206.3:c.281C>A"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_000206.3(IL2RG):c.281C>A (p.Ser94Ter)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://genboree.org/evrepo/api/summarysrvc",
      "when": "2026-06-21T04:59:53.662Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}