NEO PanTracer Tissue

PanTracer Tissue is a broad, next‑generation sequencing panel for pan‑solid tumor indications. The assay detects single nucleotide variants (SNV), insertions/deletions (InDels), copy number variants (CNV), and RNA fusions and splice variants across a comprehensive gene set, plus microsatellite instability (MSI) and tumor mutational burden (TMB).

NGS (517 total genes: DNA analysis across 517 genes; RNA fusion/splice analysis across 55 of these genes)

Immunotherapy Markers: MSI, TMB
* MSI-high is defined as ≥20% of loci showing instability; microsatellite-stable (MSS) is defined as <20% of loci showing instability.
* TMB-high is defined as ≥10.0 mutations per megabase (mut/Mb); TMB-low is defined as <10.0 mut/Mb

Legacy Test information:
As of May 29, 2025, this test serves as replacement for the following test:
* Neo Comprehensive – Solid Tumor

Specimen Requirements

A block is preferred for testing: >20% tumor and >5 mm2 of tissue surface area for NGS (~500 tumor cells)(additional 100 neoplastic cells for PD-L1). If submitting 5-micron unstained slides, the following number of slides are requested: Samples with >25 mm2 of tissue: 10 unstained slides (2 sections per slide preferred) Samples with 10-24 mm2 of tissue: 20 unstained slides (2 sections per slide preferred) Please submit 1 additional unstained slide for H&E and 3 additional unstained slides if performing PD-L1 testing.

Storage and Transportation

NYS clients please provide date and time of Collection. Use cold pack for transport, making sure cold pack is not in direct contact with specimen.

CPT Code(s)*

81459x1. Add 88360x1 for PD-L1 IHC.
Turnaround time
8-10 Days

Level of Service

  • Global

Integrations

  • Epic Aura

See all integrations →

New York Approved: Yes

*The CPT codes provided with our test descriptions are based on AMA guidelines and are for informational purposes only. Correct CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed.

Biomarkers

DNA Sequencing
SNVs + Indels
ABL1ABL2ABRAXAS1ACVR1ACVR1BADGRA2
AKT1AKT3ALOX12BAMER1ANKRD11ANKRD26
APCARAFARFRP1ARID1AARID1BARID2
ARID5BASXL1ASXL2ATRATRXAURKA
AURKBAXIN1AXIN2AXLB2MBAP1
BARD1BBC3BCL10BCL2BCL2L1BCL2L11
BCL2L2BCL6BCORBCORL1BCRBIRC3
BLMBMPR1ABRD4BRIP1BTG1BTK
CALRCARD11CASP8CBFBCBLCCN6
CCND2CD274CD276CD74CD79ACD79B
CDC73CDH1CDK12CDKN1ACDKN1BCDKN2A
CDKN2BCDKN2CCEBPACENPACHD2CHD4
CICCOP1CREBBPCRKLCRLF2CSF1R
CSF3RCSNK1A1CTCFCTLA4CTNNA1CTNNB1
CUL3CUX1CXCR4CYLDDAXXDCUN1D1
DDR2DDX41DHX15DICER1DIS3DNAJB1
DNMT1DNMT3ADNMT3BDOT1LE2F3EED
EGFL7EIF1AXEIF4A2EIF4EELOCEML4
EMSYEP300EPCAMEPHA3EPHA5EPHA7
EPHB1ERBB2ERBB4ERCC3ERCC4ERCC5
ERGERRFI1ETS1ETV1ETV4ETV5
ETV6EWSR1EZH2FANCAFANCCFANCD2
FANCEFANCFFANCGFANCIFANCLFAS
FAT1FBXW7FHFLCNFLI1FLT1
FLT3FLT4FOXA1FOXL2FOXO1FOXP1
FRS2FUBP1FYNGABRA6GATA1GATA2
GATA3GATA4GATA6GEN1GID4GLI1
GNA11GNA13GNAQGNASGPS2GREM1
GRIN2AGRM3GSK3BH1-2H2BC5H3-3A
H3-3BH3-4H3-5H3C1H3C10H3C11
H3C12H3C13H3C14H3C15H3C2H3C3
H3C4H3C6H3C7H3C8HGFHNF1A
HNRNPKHOXB13HRASHSD3B1HSP90AA1ICOSLG
ID3IDH1IDH2IFNGR1IGF1IGF1R
IGF2IKBKEIKZF1IL10IL7RINHA
INHBAINPP4AINPP4BINSRIRF2IRF4
IRS1IRS2JAK1JAK3JUNKAT6A
KDM5AKDM5CKDM6AKDRKEAP1KEL
KIF5BKLF4KLHL6KMT2AKMT2AT3LATS1
LATS2LMO1LRP1BLYNLZTR1MAGI2
MALT1MAP2K1MAP2K2MAP2K4MAP3K1MAP3K13
MAP3K14MAP3K4MAPK1MAPK3MAXMCL1
MDC1MED12MEF2BMEN1MGAMITF
MLH1MPLMRE11MSH2MSH3MSH6
MST1MST1RMTORMUTYHMYBMYD88
MYOD1NAB2NBNNCOA3NCOR1NEGR1
NF1NF2NFE2L2NFKBIANKX2-1NKX3-1
NOTCH1NOTCH2NOTCH3NOTCH4NPM1NSD1
NTRK1NTRK2NTRK3NUP93NUTM1PAK1
PAK3PAK5PALB2PARP1PAX3PAX5
PAX7PAX8PBRM1PDCD1PDCD1LG2PDGFRA
PDPK1PGRPHF6PHOX2BPIK3C2BPIK3C2G
PIK3C3PIK3CDPIK3CGPIK3R1PIK3R2PIK3R3
PIM1PLCG2PLK2PMAIP1PMS1PMS2
PNRC1POLD1POLEPPARGPPM1DPPP2R1A
PPP2R2APPP6CPRDM1PREX2PRKAR1APRKCI
PRKDCPRKNPRSS8PTCH1PTPN11PTPRD
PTPRSPTPRTQKIRAB35RAC1RAD21
RAD50RAD51RAD51BRAD51CRAD51DRAD52
RAD54LRANBP2RARARASA1RB1RBM10
RECQL4RELRHEBRHOARIT1RNF43
ROS1RPS6KA4RPS6KB2RPTORRUNX1RUNX1T1
RYBPSDHASDHAF2SDHBSDHCSDHD
SETBP1SETD2SF3B1SH2B3SH2D1ASHQ1
SLIT2SLX4SMAD2SMAD3SMAD4SMARCA4
SMARCB1SMARCD1SMC1ASMC3SMOSNCAIP
SOCS1SOX10SOX17SOX2SOX9SPEN
SPOPSPTA1SRCSRSF2STAG1STAG2
STAT3STAT4STAT5ASTAT5BSTK11STK40
SUFUSUZ12SYKTAF1TBX3TCF3
TCF7L2TENT5CTERCTERTTET1TET2
TFE3TGFBR1TGFBR2TMEM127TMPRSS2TNFAIP3
TNFRSF14TOP1TOP2ATP53TP63TRAF2
TRAF7TSC1TSC2TSHRU2AF1VEGFA
VHLVTCN1WT1XIAPXPO1XRCC2
YAP1YES1ZBTB2ZBTB7AZFHX3ZNF217
ZNF703ZRSR2
CNVs
AKT2ALKARATMBRAFBRCA1
BRCA2CCND1CCND3CCNE1CDK4CDK6
CDK8CHEK1CHEK2EGFRERBB2ERBB3
ERCC1ERCC2ESR1FGF1FGF10FGF14
FGF19FGF2FGF23FGF3FGF4FGF5
FGF6FGF7FGF8FGF9FGFR1FGFR2
FGFR3FGFR4JAK2KITKRASLAMP1
MDM2MDM4METMYCMYCL1MYCN
NRASNRG1PDGFRAPDGFRBPIK3CAPIK3CB
PTENRAF1RETRICTORRPS6KB1TFRC
Genomic Signatures
MSITMB
RNA Sequencing
Fusions
ABL1AKT3ALKAXLBRAFBRCA1
BRCA2CDK4CSF1REML4ERBB2ERG
ESR1ETS1ETV1ETV4ETV5ETV6
EWSR1FGFR1FGFR2FGFR3FGFR4FLI1
FLT1FLT3JAK2KDRKIF5BKIT
KMT2AKMT2AT3MSH2MYCNOTCH1NOTCH2
NOTCH3NRG1NTRK1NTRK2NTRK3PAX3
PAX7PDGFRAPDGFRBPIK3CAPPARGRAF1
RETROS1RPS6KB1TMPRSS2
Splice Variant
ARAR-V7
EGFREGFRvIII
METMET exon 14 Skipping

Last Updated: April 28, 2026

Get in touch

Our Client Services team is on hand to help. Please call us at 866.776.5907, Option 3.