Test 200.
Analysis of extended panel of genes for Family Oncology Diseases and Interpretation
Mutations in 233 genes associated with oncology diseases
BRCA1, BRCA2, MLH1, MSH2, MSH6, TP53, ATM, BMPR1A, CDH1, CHEK2, MUTYH, PTEN, STK11, BRIP1, NBN, PALB2, NF1, RAD51C, RAD51D, EPCAM, PMS2, APC, BUB1B, SMAD4, BLM, KIT, RET, MEN1, BAP1, CDKN2A, DICER1, EGFR, ERCC2, ERCC3, ERCC4, ERCC5, HOXB13, NSD1, PMS1, PRF1, PRKAR1A, EZH2, HRAS, CEBPA, GATA2, RUNX1, RB1, WT1, VHL, SDHD, MAX, SDHAF2, SDHB, SDHC, TMEM127, PTCH1, TSC1, TSC2, NF2, ALK, PHOX2B, SUFU, SMARCB1, CDKN1C, GPC3, CEP57, FANCD2, SLX4, XPA, FH, MET, CDC73, AIP, CYLD, DDB2, DIS3L2, EXT1, EXT2, FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FLCN, HNF1A, RECQL4, RHBDF2, SBDS, WRN, XPC