Quest Diagnostics offers a comprehensive menu of solid tumor testing solutions comprising panels and individually orderable components.
Quest Diagnostics offers a comprehensive menu of solid tumor testing solutions comprising panels and individually orderable components.
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. |
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
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Quest offers a range of disease-specific molecular genotyping panels to help prioritize treatment.
Test name | Test Code |
LungSEQ Panel | |
LungSEQ Concurrent Panel, without PD-L1a | |
ColonSEQ Panel | |
ColonSEQPlus Panel | |
MelanomaSEQ Panel | |
MelanomaSEQPlus Panel | |
Thyroid Mutation Cancer Panel
Includes BRAF Mutation Analysis, RAS Mutation Analysis, RET/PTC Rearrangement, PAX8/PPAR[gamma] Translocation |
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 | |
PIK3CA Mutation Analysis | |
NRAS Mutation Analysis (exons 1&2 - DNA sequencing) | |
KRAS Mutation Analysis (exons 1&2 - DNA | |
BRAF Mutation Analysis | |
BRAF Mutation Analysis, Papillary Thyroid Cancer | |
RAS MUTATION ANALYSIS, THYROID CANCER | |
RET/PTC Rearrangement Thyroid Cancer | |
PAX8/PPAR[gamma] Translocation, Thyroid Cancer | |
MELANOMA, BRAF V600 MUTATION, COBAS | |
EGFR MUTATION, COBAS V2, LIQUID BIOPSY | |
Epidermal Growth Factor Receptor (EGFR) Mutation, Cobas V2, Solid Tumor | |
PDGFRA Mutation Analysis |
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
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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
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Hereditary Breast Cancer Panel | Test Code |
ATM, BARD1, BRCA1, BRCA2, CHEK2, CDH1, EPCAM, MLH1, MSH2, MSH6, NF1, PALB2, PMS2, PTEN, RAD51C, RAD51D, STK11, TP53
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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
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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 | |
ATM Sequencing and Deletion/Duplication | |
BAP1 Sequencing and Deletion/Duplication | |
BLM Sequencing and Deletion/Duplication | |
CDH1 Sequencing and Deletion/Duplication | |
CDKN2A Sequencing and Deletion/Duplication | |
CHEK2 Sequencing and Deletion/Duplication | |
Lynch Syndrome, MSH2 Sequencing and Deletion/Duplication (Including EPCAM) | |
FH Gene Sequencing and Deletion/Duplication | |
FLCN Sequencing and Deletion/Duplication | |
HOXB13 Sequencing and Deletion/Duplication | |
MEN1 Sequencing and Deletion/Duplication | |
MITF Gene Analysis | |
Lynch Syndrome, MLH1 Sequencing and Deletion/Duplication | |
Lynch Syndrome, MSH6 Sequencing and Deletion/Duplication | |
MUTYH Sequencing and Deletion/Duplication | |
NF1 Sequencing and Deletion/Duplication | |
PALB2 Sequencing and Deletion/Duplication | |
Lynch Syndrome, PMS2 Sequencing and Deletion/Duplication | |
PTEN Sequencing and Deletion/Duplication | |
RET Sequencing and Deletion/Duplication | |
SMARCA4 Sequencing and Deletion/Duplication | |
STK11 Sequencing and Deletion/Duplication | |
Li-Fraumeni Syndrome, TP53 Sequencing and Deletion/Duplication | |
VHL Sequencing and Deletion/Duplication |
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
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| 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
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