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Lab reportcohort · india-sim

10/30/2026, 1:56:59 PM · PharmCAT 3.4.0 · Research record, not medical advice

2
Genes standardised
2
Calls quoted
6
Coverage gaps
0
Identifiers removed
27.8s
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  1. Muse Sparkread 2 gene calls13.8s
  2. PharmCATstandardised 2 genes14.0s
  3. Rules6 coverage gaps

CallsMuse Spark each call quoted from the source, then standardised by PharmCAT

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GeneAs printedStandardisedPhenotype term
DPYD“DPYD. The patient carries DPYD c.85T>C (*9A) heterozygous. Predicted DPD phenotype: normal metabolizer (activity score 2).”Reference/c.85T>C (*9A)one copy *9ANormal Metabolizer · activity 2.0
UGT1A1“UGT1A1. Genotype *1/*1 (TA6/TA6), consistent with a normal metabolizer.”*1/*1Normal Metabolizer

Method as printed: Method: targeted genotyping by real-time PCR. Only the listed variants are assayed; variants outside this panel cannot be excluded.

Coveragedeterministic rules · which India-relevant variants this panel named

DPYDHapB3not in this panel

Most common Indian decreased-function DPYD variant (~3.3%, PMID 40810747)

DPYDc.85T>C (*9A)named on the report

~25% in Indians; toxicity signal in South Indian cohorts (PMC11300675)

DPYD*2Anot in this panel

European tier-1 variant; rare in Indians (PMID 40810747)

DPYD*13not in this panel

Tier-1 no-function variant (PMID 39032821)

DPYDc.2846A>Tnot in this panel

Tier-1 variant; near-absent in Indians (PMID 40810747)

UGT1A1*28not in this panel

TA-repeat allele, common in South Asians

UGT1A1*6not in this panel

East Asian allele; reported at low frequency in India

A variant the panel did not name is left out of cohort statistics for that variant, rather than counted as absent. Reader notes: 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.

Exportde-identified · the same record in three formats

Curator review

A curator checks each call against the source document before the record counts in a cohort, and Muse Spark web search finds published Indian frequency data for each variant. Both are written to the audit log. Reviewing is the one action that needs a curator code, because it is a claim that a person checked the page.

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Research tool, not medical advice. Pathya reads and standardises pharmacogenomic results; it makes no dose, drug or test recommendation. Audit log: data/cases/79d8fbba0108/audit.log.