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Precision Oncology Tests

Comprehensive precision medicine solutions for solid tumors

Quest Diagnostics offers a comprehensive menu of solid tumor testing solutions comprising panels and individually orderable components.

Comprehensive genomic profiling

With just one test, an expanded comprehensive genomic profiling (CGP) panel detects information across hundreds of genes. Tumor testing with CGP provides you with the most up-to-date information to help you navigate emerging therapies beyond the current standard of care. 

LiquidSEQTM

Test Code

ABL1, ABL2, ABRAXAS1, ACVR1, ACVR1B, ADGRA2, AKT1, AKT2, AKT3, ALK, ALOX12B, ANKRD11, ANKRD26, APC, AR, ARAF, ARFRP1, ARID1A, ARID1B, ARID2, ARID5B, ASXL1, ASXL2, ATM, ATR, ATRX, AURKA, AURKB, AXIN1, AXIN2, AXL, B2M, BAP1, BARD1, BBC3, BCL10, BCL2, BCL2L1, BCL2L11, BCL2L2, BCL6, BCOR, BCORL1, BCR, BIRC3, BLM, BMPR1A, BRAF, BRCA1, BRCA2, BRD4, BRIP1, BTG1, BTK, CALR, CARD11, CASP8, CBFB, CBL, CCN6, CCND1, CCND2, CCND3, CCNE1, CD274, CD276, CD74, CD79A, CD79B, CDC73, CDH1, CDK12, CDK4, CDK6, CDK8, CDKN1A, CDKN1B, CDKN2A, CDKN2B, CDKN2C, CEBPA, CENPA, CHD2, CHD4, CHEK1, CHEK2, CIC, COP1, CREBBP, CRKL, CRLF2, CSF1R, CSF3R, CSNK1A1, CTCF, CTLA4, CTNNA1, CTNNB1, CUL3, CUX1, CXCR4, CYLD, DAXX, DCUN1D1, DDR2, DDX41, DHX15, DICER1, DIS3, DNAJB1, DNMT1, DNMT3A, DNMT3B, DOT1L, E2F3, EED, EGFL7, EGFR, EIF1AX, EIF4A2, EIF4E, ELOC, EML4, EMSY, EP300, EPCAM, EPHA3, EPHA5, EPHA7, EPHB1, ERBB2, ERBB3, ERBB4, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, ERG, ERRFI1, ESR1, ETS1, ETV1, ETV4, ETV5, ETV6, EWSR1, EZH2, FAM123B, FANCA, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FAS, FAT1, FBXW7, FGF1, FGF10, FGF14, FGF19, FGF2, FGF23, FGF3, FGF4, FGF5, FGF6, FGF7, FGF8, FGF9, FGFR1, FGFR2, FGFR3, FGFR4, FH, FLCN, FLI1, FLT1, FLT3, FLT4, FOXA1, FOXL2, FOXO1, FOXP1, FRS2, FUBP1, FYN, GABRA6, GATA1, GATA2, GATA3, GATA4, GATA6, GEN1, GID4, GLI1, GNA11, GNA13, GNAQ, GNAS, GPS2, GREM1, GRIN2A, GRM3, GSK3B, H1-2, H2BC5, H3-3A, H3-3B, H3-4, H3-5, H3C1, H3C2, H3C3, H3C4, H3C6, H3C7, H3C8, H3C10, H3C11, H3C12, H3C13, H3C14, H3C15, HGF, HLA-A, HLA-B, HLA-C, HNF1A, HNRNPK, HOXB13, HRAS, HSD3B1, HSP90AA1, ICOSLG, ID3, IDH1, IDH2, IFNGR1, IGF1, IGF1R, IGF2, IKBKE, IKZF1, IL10, IL7R, INHA, INHBA, INPP4A, INPP4B, INSR, IRF2, IRF4, IRS1, IRS2, JAK1, JAK2, JAK3, JUN, KAT6A, KDM5A, KDM5C, KDM6A, KDR, KEAP1, KEL, KIF5B, KIT, KLF4, KLHL6, KMT2B, KMT2C, KMT2D, KRAS, LAMP1, LATS1, LATS2, LMO1, LRP1B, LYN, LZTR1, MAGI2, MALT1, MAP2K1, MAP2K2, MAP2K4, MAP3K1, MAP3K13, MAP3K14, MAP3K4, MAPK1, MAPK3, MAX, MCL1, MDC1, MDM2, MDM4, MED12, MEF2B, MEN1, MET, MGA, MITF, MLH1, MLL, MLLT3, MPL, MRE11, MSH2, MSH3, MSH6, MST1, MST1R, MTOR, MUTYH, MYB, MYC, MYCL, MYCN, MYD88, MYOD1, NAB2, NBN, NCOA3, NCOR1, NEGR1, NF1, NF2, NFE2L2, NFKBIA, NKX2-1, NKX3-1, NOTCH1, NOTCH2, NOTCH3, NOTCH4, NPM1, NRAS, NRG1, NSD1, NTRK1, NTRK2, NTRK3, NUP93, NUTM1, PAK1, PAK3, PAK5, PALB2, PARP1, PAX3, PAX5, PAX7, PAX8, PBRM1, PDCD1, PDCD1LG2, PDGFRA, PDGFRB, PDK1, PDPK1, PGR, PHF6, PHOX2B, PIK3C2B, PIK3C2G, PIK3C3, PIK3CA, PIK3CB, PIK3CD, PIK3CG, PIK3R1, PIK3R2, PIK3R3, PIM1, PLCG2, PLK2, PMAIP1, PMS1, PMS2, PNRC1, POLD1, POLE, PPARG, PPM1D, PPP2R1A, PPP2R2A, PPP6C, PRDM1, PREX2, PRKAR1A, PRKCI, PRKDC, PRKN, PRSS8, PTCH1, PTEN, PTPN11, PTPRD, PTPRS, PTPRT, QKI, RAB35, RAC1, RAD21, RAD50, RAD51, RAD51B, RAD51C, RAD51D, RAD52, RAD54L, RAF1, RANBP2, RARA, RASA1, RB1, RBM10, RECQL4, REL, RET, RHEB, RHOA, RICTOR, RIT1, RNF43, ROS1, RPS6KA4, RPS6KB1, RPS6KB2, RPTOR, RUNX1, RUNX1T1, RYBP, SDHA, SDHAF2, SDHB, SDHC, SDHD, SETBP1, SETD2, SF3B1, SH2B3, SH2D1A, SHQ1, SLIT2, SLX4, SMAD2, SMAD3, SMAD4, SMARCA4, SMARCB1, SMARCD1, SMC1A, SMC3, SMO, SNCAIP, SOCS1, SOX10, SOX17, SOX2, SOX9, SPEN, SPOP, SPTA1, SRC, SRSF2, STAG1, STAG2, STAT3, STAT4, STAT5A, STAT5B, STK11, STK40, SUFU, SUZ12, SYK, TAF1, TBX3, TCF3, TCF7L2, TENT5C, TERC, TERT, TET1, TET2, TFE3, TFRC, TGFBR1, TGFBR2, TMEM127, TMPRSS2, TNFAIP3, TNFRSF14, TOP1, TOP2A, TP53, TP63, TRAF2, TRAF7, TSC1, TSC2, TSHR, U2AF1, VEGFA, VHL, VTCN1, WT1, XIAP, XPO1, XRCC2, YAP1, YES1, ZBTB2, ZBTB7A, ZFHX3, ZNF217, ZNF703, and ZRSR2. Includes TMB and MSI analysis.

14308

Solid TumorSEQTM

Test Code

Includes assessment of all DNA variant types for all genes listed for LiquidSEQ™ above, with additional testing of 55 genes for RNA fusions

ABL1, AKT3, ALK, AR, AXL, BCL2, BRAF, BRCA1, BRCA2, CDK4, CSF1R, EGFR, EML4, ERBB2, ERG, ESR1, ETS1, ETV1, ETV4, ETV5, EWSR1, FGFR1, FGFR2, FGFR3, FGFR4, FLI1, FLT1, FLT3, JAK2, KDR, KIF5B, KIT, MET, MLL, MLLT3, MSH2, MYC, NOTCH1, NOTCH2, NOTCH3, NRG1, NTRK1, NTRK2, NTRK3, PAX3, PAX7, PDGFRA, PDGFRB, PIK3CA, PPARG, RAF1, RET, ROS1, RPS6KB1, and TMPRSS2 (splice site analysis also performed for AR, EGFR, and MET). Includes TMB and MSI analysis

 

143089

Disease-specific panels

Quest offers a range of disease-specific molecular genotyping panels to help prioritize treatment.

Test name

Test Code

LungSEQ Panel

Includes KT1, ALK, BRAF, EGFR, ERBB2, KRAS, MAP2K1, NRAS,
PIK3CA,
and PTEN

36915

LungSEQ Concurrent Panel, without PD-L1a

Includes LK, AKT1, BRAF, EGFR, ERBB2, KRAS, MAP2K1, NRAS, PIK3CA, and PTEN. Also includes: ALK Rearrangement, RET Rearrangement, ROS1 Rearrangement, and MET Amplification

12184

ColonSEQ Panel

Includes BRAF, KRAS, NRAS, MSI (PCR), PIK3CA, PTEN

36918

ColonSEQPlus Panel

Includes APC, BRAF, CTNNB1, EGFR, ERBB2 (HER2), FBXW7, KRAS, MET, NRAS, PIK3CA, PTEN, SMAD4, TP53 with microsatellite instability (MSI)

36919

MelanomaSEQ Panel

Includes BRAF, c-KIT, NRAS

36914

MelanomaSEQPlus Panel

Includes BRAF, c-KIT, CTNNB1, GNA11, GNAQ, GNAS, HRAS, KRAS, NRAS, PIK3CA, PTEN

36912

Thyroid Mutation Cancer Panel

 

Includes BRAF Mutation Analysis, RAS Mutation Analysis, RET/PTC Rearrangement, PAX8/PPAR[gamma] Translocation

90469

Somatic solid tumor single-gene tests

We offer a range of individually orderable components for somatic genes to allow greater insight for specific targets.

Test name

Test Code

c-KIT Mutation Analysis, PCR

19961

PIK3CA Mutation Analysis

16897

NRAS Mutation Analysis (exons 1&2 - DNA sequencing)

16818

KRAS Mutation Analysis (exons 1&2 - DNA

16510

BRAF Mutation Analysis

16767

BRAF Mutation Analysis, Papillary Thyroid Cancer

90477

RAS MUTATION ANALYSIS, THYROID CANCER

90479

RET/PTC Rearrangement Thyroid Cancer

90473

PAX8/PPAR[gamma] Translocation, Thyroid Cancer

90474

MELANOMA, BRAF V600 MUTATION, COBAS

90956

EGFR MUTATION, COBAS V2, LIQUID BIOPSY

94718

Epidermal Growth Factor Receptor (EGFR) Mutation, Cobas V2, Solid Tumor

94719

PDGFRA Mutation Analysis

16859

Hereditary cancer testing

We offer advanced hereditary cancer testing so that you and your patients can understand their potential risk for cancer and, in some cases, inform treatment and prognosis. From comprehensive panels to single-gene tests, our complete portfolio of hereditary cancer tests delivers accessible, actionable insights efficiently and affordably. 

Comprehensive Hereditary Cancer Panel

Test Code

APC, ATM, AXIN2, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN1B, CDKN2A (p16, p14), CHEK2, DICER1, EGFR, EPCAM, FANCA, FANCC, FANCM, FH, FLCN, GALNT12, GREM1, HOXB13, MAX, MEN1, MET, MITF, MLH1, MRE11, (MRE11A), MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NTHL1, PALB2, PMS2, POLD1, POLE, POT1, PTCH1, PTEN, RAD50, RAD51C, RAD51D, RECQL, RET, SDHA, SDHAF2, SDHB, SDHC, SDHD, SMARCA4, SMAD4, STK11, SUFU, TMEM127, TP53, TSC1, TSC2, VHL, XRCC2

 

38600

Guideline Based Hereditary Cancer Panel

Test Code

APC, ATM, AXIN2, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A (p16, p14), CHEK2, EPCAM, GREM1, HOXB13, MLH1, MSH2, MSH3, MSH6, MUTYH, NF1, NTHL1, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53

 

38611

Hereditary Breast Cancer Panel

Test Code

ATM, BARD1, BRCA1, BRCA2, CHEK2, CDH1, EPCAM, MLH1, MSH2, MSH6, NF1, PALB2, PMS2, PTEN, RAD51C, RAD51D, STK11, TP53

 

38621

Hereditary Colorectal Cancer Panel

Test Code

APC, AXIN2, BMPR1A, CDH1, CHEK2, EPCAM, GREM1, MLH1, MSH2, MSH3, MSH6, MUTYH, NTHL1, PMS2, POLD1, POLE, PTEN, SMAD4, STK11, TP53

 

38631

Individually orderable hereditary testing components

We offer a range of individually orderable components for hereditary genes to allow greater insight for specific targets.

Test name

Test code

APC Sequencing and Deletion/Duplication

93797

ATM Sequencing and Deletion/Duplication

38802

BAP1 Sequencing and Deletion/Duplication

38803

BLM Sequencing and Deletion/Duplication

38804

CDH1 Sequencing and Deletion/Duplication

92568

CDKN2A Sequencing and Deletion/Duplication

93939

CHEK2 Sequencing and Deletion/Duplication

93940

Lynch Syndrome, MSH2 Sequencing and Deletion/Duplication (Including EPCAM)

91471

FH Gene Sequencing and Deletion/Duplication

38805

FLCN Sequencing and Deletion/Duplication

38806

HOXB13 Sequencing and Deletion/Duplication

38807

MEN1 Sequencing and Deletion/Duplication

93942

MITF Gene Analysis

38808

Lynch Syndrome, MLH1 Sequencing and Deletion/Duplication

91460

Lynch Syndrome, MSH6 Sequencing and Deletion/Duplication

91458

MUTYH Sequencing and Deletion/Duplication

93944

NF1 Sequencing and Deletion/Duplication

93941

PALB2 Sequencing and Deletion/Duplication

92571

Lynch Syndrome, PMS2 Sequencing and Deletion/Duplication

91457

PTEN Sequencing and Deletion/Duplication

92566

RET Sequencing and Deletion/Duplication

93796

SMARCA4 Sequencing and Deletion/Duplication

38809

STK11 Sequencing and Deletion/Duplication

92565

Li-Fraumeni Syndrome, TP53 Sequencing and Deletion/Duplication

92560

VHL Sequencing and Deletion/Duplication

93943

Pharmacogenomics

Our pharmacogenomics offerings analyze genes with clinically actionable pharmacogenetic associations supported by insights from expert groups like the Clinical Pharmacogenetics Implementation Consortium (CPIC) and ClinPGx. A single test can inform decisions across a broad range of clinical areas. 

Pharmacogenomics Panel with Coriell Life Sciences (CLS) Report

Test Code

ABCG2, CYP2B6, CYP2C9, CYP2C19, CYP2D6, CYP3A4, CYP3A5, CYP4F2, DPYD F5, HLA-A*31:01, HLA-B*15:02, HLA-B*57:01, HLA-B*58:01, IFNL3, NAT2, NUDT15, SLCO1B1, TPMT, UGT1A1, VKORC1

 

14271

 

DPYD Genotype

Test Code

c.1905+1G>A, c.295_298delTCAT, c.703C>T, c.2983G>T, c.1156G>T, c.1679T>G, c.557A>G, c.2846A>T, c.61C>T, c.1129-5923C>G, c.2279C>T, c.868A>G

 

18753

 

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