{
  "record": {
    "id": "dc893b814599",
    "label": "IndiPGx-Pop p115",
    "cohort": "india-sim",
    "source": "report",
    "createdAt": "2026-10-30T13:58:07.288Z"
  },
  "calls": [
    {
      "gene": "DPYD",
      "diplotype": "Reference/Reference",
      "phenotype": "Normal Metabolizer",
      "activityScore": "2.0",
      "source": "OUTSIDE"
    },
    {
      "gene": "UGT1A1",
      "diplotype": "*1/*28",
      "phenotype": "Intermediate Metabolizer",
      "source": "OUTSIDE"
    }
  ],
  "extract": {
    "genes": [
      {
        "activityScore": "",
        "diplotype": "Reference/Reference",
        "gene": "DPYD",
        "phenotype": "Normal metabolizer",
        "verbatim": "DPYD Phenotype: Normal metabolizer c.1905+1G>A (*2A) Not detected c.1679T>G (*13) Not detected c.2846A>T Not detected"
      },
      {
        "activityScore": "",
        "diplotype": "*1/*28",
        "gene": "UGT1A1",
        "phenotype": "Intermediate metabolizer",
        "verbatim": "UGT1A1 Phenotype: Intermediate metabolizer *28 Detected (heterozygous)"
      }
    ],
    "labName": "Example Pharmacogenomics Centre, Mumbai",
    "methodNotes": "Sample: peripheral blood (EDTA). Method: targeted genotyping by real-time PCR. Only the listed variants are assayed; DPYD tested for c.1905+1G>A (*2A), c.1679T>G (*13), c.2846A>T; UGT1A1 tested for *28; variants outside this panel cannot be excluded.",
    "patientRef": "",
    "reportDate": "28 Oct 2026",
    "testedVariants": [
      {
        "gene": "DPYD",
        "variant": "c.1905+1G>A (*2A)"
      },
      {
        "gene": "DPYD",
        "variant": "c.1679T>G (*13)"
      },
      {
        "gene": "DPYD",
        "variant": "c.2846A>T"
      },
      {
        "gene": "UGT1A1",
        "variant": "*28"
      }
    ],
    "warnings": [
      "Only the listed variants are assayed; variants outside this panel cannot be excluded.",
      "Synthetic document generated for software benchmarking. Not a real patient or laboratory."
    ]
  },
  "quality": {
    "identifierRemoved": true,
    "unread": [],
    "coverage": [
      {
        "gene": "DPYD",
        "variant": "HapB3",
        "stated": false,
        "why": "Most common Indian decreased-function DPYD variant (~3.3%, PMID 40810747)"
      },
      {
        "gene": "DPYD",
        "variant": "c.85T>C (*9A)",
        "stated": false,
        "why": "~25% in Indians; toxicity signal in South Indian cohorts (PMC11300675)"
      },
      {
        "gene": "DPYD",
        "variant": "*2A",
        "stated": true,
        "why": "European tier-1 variant; rare in Indians (PMID 40810747)"
      },
      {
        "gene": "DPYD",
        "variant": "*13",
        "stated": true,
        "why": "Tier-1 no-function variant (PMID 39032821)"
      },
      {
        "gene": "DPYD",
        "variant": "c.2846A>T",
        "stated": true,
        "why": "Tier-1 variant; near-absent in Indians (PMID 40810747)"
      },
      {
        "gene": "UGT1A1",
        "variant": "*28",
        "stated": true,
        "why": "TA-repeat allele, common in South Asians"
      },
      {
        "gene": "UGT1A1",
        "variant": "*6",
        "stated": false,
        "why": "East Asian allele; reported at low frequency in India"
      }
    ],
    "warnings": [
      "Only the listed variants are assayed; variants outside this panel cannot be excluded.",
      "Synthetic document generated for software benchmarking. Not a real patient or laboratory."
    ]
  },
  "review": null,
  "pharmcat": {
    "version": "3.4.0",
    "data": "2026-07-13-11-40"
  },
  "note": "Research record. Not medical advice."
}