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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
ABL1ABL2
ABRAXAS1ACVR1
ACVR1BADGRA2
AKT1AKT2
AKT3ALK
ALOX12BAMER1
ANKRD11ANKRD26
APCAR
ARAFARFRP1
ARID1AARID1B
ARID2ARID5B
ASXL1ASXL2
ATMATR
ATRXAURKA
AURKBAXIN1
AXIN2AXL
B2MBAP1
BARD1BBC3
BCL10BCL2
BCL2L1BCL2L11
BCL2L2BCL6
BCORBCORL1
BCRBIRC3
BLMBMPR1A
BRAFBRCA1
BRCA2BRD4
BRIP1BTG1
BTKCALR
CARD11CASP8
CBFBCBL
CCN6CCND1
CCND2CCND3
CCNE1CD274
CD276CD74
CD79ACD79B
CDC73CDH1
CDK12CDK4
CDK6CDK8
CDKN1ACDKN1B
CDKN2ACDKN2B
CDKN2CCEBPA
CENPACHD2
CHD4CHEK1
CHEK2CIC
COP1CREBBP
CRKLCRLF2
CSF1RCSF3R
CSNK1A1CTCF
CTLA4CTNNA1
CTNNB1CUL3
CUX1CXCR4
CYLDDAXX
DCUN1D1DDR2
DDX41DHX15
DICER1DIS3
DNAJB1DNMT1
DNMT3ADNMT3B
DOT1LE2F3
EEDEGFL7
EGFREIF1AX
EIF4A2EIF4E
ELOCEML4
EMSYEP300
EPCAMEPHA3
EPHA5EPHA7
EPHB1ERBB2
ERBB3ERBB4
ERCC1ERCC2
ERCC3ERCC4
ERCC5ERG
ERRFI1ESR1
ETS1ETV1
ETV4ETV5
ETV6EWSR1
EZH2FANCA
FANCCFANCD2
FANCEFANCF
FANCGFANCI
FANCLFAS
FAT1FBXW7
FGF1FGF10
FGF14FGF19
FGF2FGF23
FGF3FGF4
FGF5FGF6
FGF7FGF8
FGF9FGFR1
FGFR2FGFR3
FGFR4FH
FLCNFLI1
FLT1FLT3
FLT4FOXA1
FOXL2FOXO1
FOXP1FRS2
FUBP1FYN
GABRA6GATA1
GATA2GATA3
GATA4GATA6
GEN1GID4
GLI1GNA11
GNA13GNAQ
GNASGPS2
GREM1GRIN2A
GRM3GSK3B
H1-2H2BC5
H3-3AH3-3B
H3-4H3-5
H3C1H3C10
H3C11H3C12
H3C13H3C14
H3C15H3C2
H3C3H3C4
H3C6H3C7
H3C8HGF
HNF1AHNRNPK
HOXB13HRAS
HSD3B1HSP90AA1
ICOSLGID3
IDH1IDH2
IFNGR1IGF1
IGF1RIGF2
IKBKEIKZF1
IL10IL7R
INHAINHBA
INPP4AINPP4B
INSRIRF2
IRF4IRS1
IRS2JAK1
JAK2JAK3
JUNKAT6A
KDM5AKDM5C
KDM6AKDR
KEAP1KEL
KIF5BKIT
KLF4KLHL6
KRASLAMP1
LATS1LATS2
LMO1LRP1B
LYNLZTR1
MAGI2MALT1
MAP2K1MAP2K2
MAP2K4MAP3K1
MAP3K13MAP3K14
MAP3K4MAPK1
MAPK3MAX
MCL1MDC1
MDM2MDM4
MED12MEF2B
MEN1MET
MGAMITF
MLH1MLL
MLLT3MPL
MRE11MSH2
MSH3MSH6
MST1MST1R
MTORMUTYH
MYBMYC
MYCLMYCN
MYD88MYOD1
NAB2NBN
NCOA3NCOR1
NEGR1NF1
NF2NFE2L2
NFKBIANKX2-1
NKX3-1NOTCH1
NOTCH2NOTCH3
NOTCH4NPM1
NRASNRG1
NSD1NTRK1
NTRK2NTRK3
NUP93NUTM1
PAK1PAK3
PAK5PALB2
PARP1PAX3
PAX5PAX7
PAX8PBRM1
PDCD1PDCD1LG2
PDGFRAPDGFRB
PDK1PDPK1
PGRPHF6
PHOX2BPIK3C2B
PIK3C2GPIK3C3
PIK3CAPIK3CB
PIK3CDPIK3CG
PIK3R1PIK3R2
PIK3R3PIM1
PLCG2PLK2
PMAIP1PMS1
PMS2PNRC1
POLD1POLE
PPARGPPM1D
PPP2R1APPP2R2A
PPP6CPRDM1
PREX2PRKAR1A
PRKCIPRKDC
PRKNPRSS8
PTCH1PTEN
PTPN11PTPRD
PTPRSPTPRT
QKIRAB35
RAC1RAD21
RAD50RAD51
RAD51BRAD51C
RAD51DRAD52
RAD54LRAF1
RANBP2RARA
RASA1RB1
RBM10RECQL4
RELRET
RHEBRHOA
RICTORRIT1
RNF43ROS1
RPS6KA4RPS6KB1
RPS6KB2RPTOR
RUNX1RUNX1T1
RYBPSDHA
SDHAF2SDHB
SDHCSDHD
SETBP1SETD2
SF3B1SH2B3
SH2D1ASHQ1
SLIT2SLX4
SMAD2SMAD3
SMAD4SMARCA4
SMARCB1SMARCD1
SMC1ASMC3
SMOSNCAIP
SOCS1SOX10
SOX17SOX2
SOX9SPEN
SPOPSPTA1
SRCSRSF2
STAG1STAG2
STAT3STAT4
STAT5ASTAT5B
STK11STK40
SUFUSUZ12
SYKTAF1
TBX3TCF3
TCF7L2TENT5C
TERCTERT Promoter
TET1TET2
TFE3TFRC
TGFBR1TGFBR2
TMEM127TMPRSS2
TNFAIP3TNFRSF14
TOP1TOP2A
TP53TP63
TRAF2TRAF7
TSC1TSC2
TSHRU2AF1
VEGFAVHL
VTCN1WT1
XIAPXPO1
XRCC2YAP1
YES1ZBTB2
ZBTB7AZFHX3
ZNF217ZNF703
ZRSR2
CNVs
AKT2ALKARATMBRAFBRCA1
BRCA2CCND1CCND3CCNE1CDK4CDK6
CDK8CHEK1CHEK2EGFRERBB2ERBB3
ERCC1ERCC2ESR1FGF1FGF10FGF14
FGF19FGF2FGF23FGF3FGF4FGF5
FGF6FGF7FGF8FGF9FGFR1FGFR2
FGFR3FGFR4JAK2KITKRASLAMP1
MDM2MDM4METMYCMYCLMYCN
NRASNRG1PDGFRAPDGFRBPIK3CAPIK3CB
PTENRAF1RETRICTORRPS6KB1TFRC
Genomic Signatures
MSITMB
Fusions
EGFR
RNA Sequencing
Fusions
ABL1AKT3ALKARAR-V7AXL
BCL2BRAFBRCA1BRCA2CDK4CSF1R
EML4ERBB2ERGESR1ETS1ETV1
ETV4ETV5EWSR1FGFR1FGFR2FGFR3
FGFR4FLI1FLT1FLT3JAK2KDR
KIF5BKITMETMLLMLLT3MSH2
MYCNOTCH1NOTCH2NOTCH3NRG1NTRK1
NTRK2NTRK3PAX3PAX7PDGFRAPDGFRB
PIK3CAPPARGRAF1RETROS1RPS6KB1
TMPRSS2
Splice Variant
ARAR-V7
EGFREGFRvIII
EGFRvIIIMET
MET exon 14 SkippingMET exon 14 Skipping

Last Updated: August 04, 2026

Get in touch

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