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IndiPGx-Read D-r04

Lab reportcohort · demo

10/30/2026, 6:25:53 AM · PharmCAT 3.4.0 · Research record, not medical advice

3
Genes standardised
3
Calls quoted
0
Coverage gaps
1
Identifiers removed
28.7s
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  1. Muse Sparkread 3 gene calls14.9s
  2. PharmCATstandardised 3 genes13.8s
  3. Rules0 coverage gaps

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

Synthetic Genomics Lab (Kochi) · 13 Oct 2026 · open original photo

Uploaded lab report photo
GeneAs printedStandardisedPhenotype term
CYP2C19“*1/*1 / Normal metabolizer”*1/*1Normal Metabolizer
DPYD“c.1905+1G>A (*2A) heterozygous / Intermediate metabolizer (activity score 1)”Reference/c.1905+1G>A (*2A)Intermediate Metabolizer · activity 1.0
TPMT“*3A/*3C (*3B + *3C in cis) / Poor metabolizer”*3A/*3CPoor 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

DPYDHapB3named on the report

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*2Anamed on the report

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

DPYD*13named on the report

Tier-1 no-function variant (PMID 39032821)

DPYDc.2846A>Tnamed on the report

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

TPMT*3Cnamed on the report

Most common TPMT variant in South Asians

CYP2C19*2named on the report

Common no-function allele in South Asians

CYP2C19*17named on the report

Increased-function allele

A variant the panel did not name is left out of cohort statistics for that variant, rather than counted as absent. A patient or lab reference printed on the report was removed before storage. Reader notes: Only the listed variants are assayed; variants outside this panel cannot be excluded. CYP2C19 *1/*1 reflects only *2, *3, *17 tested; untested variants cannot be excluded.

Exportde-identified · the same record in three formats

Curator review

This is a read-only sample. In the pilot, 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.

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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/ad9c56a60ce0/audit.log.