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Condition
Test Name
Comprehensive Hereditary Cancer Gene panel (SNVs, small INDELs and CNVs)
Inclusive Genes
ABRAXAS1, AIP, ALK, APC, AR, ATM, AXIN2, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, BUB1B, CBL, CDC73, CDH1, CDK4, CDKN1B, CDKN1C, CDKN2A, CHEK2, CTNNA1, CYLD, DDB2, DICER1, DIS3L2, ELAC2, EPCAM, ERCC2, ERCC3, ERCC4, ERCC5, EXT1, EXT2, FAN1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FH, FLCN, GALNT12, GATA2, GPC3, HOXB13, HRAS, KIF1B, KIT, LZTR1, MAX, MEN1, MET, MITF, MLH1, MLH3, MRE11, MSH2, MSH3, MSH6, MSR1, MUTYH, NBN, NF1, NF2, NTHL1, PALB2, PAX5, PDGFRA, PHOX2B, PMS1, PMS2, POLD1, POLE, POT1, PRKAR1A, PRSS1, PTCH1, PTCH2, PTEN, RAD50, RAD51C, RAD51D, RB1, RECQL, RECQL4, RET, RHBDF2, RINT1, RNASEL, RNF43, RUNX1, SBDS, SDHA, SDHAF2, SDHB, SDHC, SDHD, SLC45A2, SLX4, SMAD4, SMARCB1, SMARCE1, SRGAP1, STK11, SUFU, TERT, TGFBR2, TMEM127, TP53, TSC1, TSC2, TYR, VHL, WRN, WT1, XPA, XPC, XRCC2, XRCC3, GREM2, SCG5
Specimen Type
Peripheral blood/purified genomic DNA