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      "label": "ClinGen Antibody Deficiencies Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for CTLA4 Version 1.0.0",
      "type": "VariantPathogenicityInterpretationGuideline",
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    },
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      "id": "MONDO:0014493",
      "label": "autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency",
      "type": "GeneticCondition"
    },
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                "@id": "https://obofoundry.org/sepio/SEPIO:0000327",
                "id": "SEPIO:0000327",
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              "id": "0080",
              "label": "BP4",
              "type": "Criterion"
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            "evidenceLine": [
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                    ],
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            ],
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            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Not Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
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        },
        "id": "CG-PCER-VARINT:CA2067131/MONDO:0014493/122/0/1684",
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      },
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                },
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                },
                "type": "Contribution"
              }
            ],
            "criterion": {
              "@id": "https://obofoundry.org/sepio/clingen/0087",
              "defaultStrength": {
                "@id": "https://obofoundry.org/sepio/SEPIO:0000325",
                "id": "SEPIO:0000325",
                "label": "Benign Stand Alone"
              },
              "id": "0087",
              "label": "BA1",
              "type": "Criterion"
            },
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA2067131/MONDO:0014493/122/el/0/1777/1779",
                "evidenceItem": [
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                          "type": "Agent"
                        },
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                          "description": "Date on which this evidence was provided"
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                      }
                    ],
                    "id": "CA2067131/MONDO:0014493/122/ci/CA2067131/MONDO:0014493/122.002",
                    "type": "InfFromBkgrndSciKnow"
                  }
                ],
                "id": "CG-PCER-VARINT:CA2067131/MONDO:0014493/122/0/1777/1779",
                "type": "EvidenceLine"
              }
            ],
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            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
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          }
        ],
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        },
        "id": "CG-PCER-VARINT:CA2067131/MONDO:0014493/122/0/1777",
        "type": "EvidenceLine"
      },
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                  "description": "Date on which this evidence was provided"
                },
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                  "@id": "https://obofoundry.org/sepio/0000156",
                  "id": "SEPIO:0000516",
                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
              }
            ],
            "criterion": {
              "@id": "https://obofoundry.org/sepio/clingen/0062",
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                "@id": "https://obofoundry.org/sepio/SEPIO:0000329",
                "id": "SEPIO:0000329",
                "label": "Pathogenic Supporting"
              },
              "id": "0062",
              "label": "PP3",
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            },
            "evidenceLine": [
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                        },
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                      }
                    ],
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                  }
                ],
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            ],
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              "@id": "SEPIO:0000224",
              "label": "Not Met"
            },
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          }
        ],
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          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA2067131/MONDO:0014493/122/0/1747",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA2067131/MONDO:0014493/122",
    "metadata": {
      "created": "2026-09-14T22:25:16.698Z",
      "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, 14 Sep 2026 22:25:16 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "1.3.0"
    },
    "statementOutcome": {
      "@id": "https://loinc.org/LA6675-8",
      "id": "LN:LA6675-8",
      "label": "Benign"
    },
    "type": "VariantPathogenicityInterpretation",
    "uuid": "a0b3a8d5-92e4-4678-a5f0-1e6bc6e1162f",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA2067131",
      "id": "CAR:CA2067131",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_005214.5:c.563A>G"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_005214.5:c.563A>G"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-10-16T23:17:06.889Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}