Cancer-NGS

Câncer hereditário: sequenciamento - 120 genes

Painel ampliado para a investigação de genes previamente associados a diferentes tipos de síndromes de câncer hereditário: câncer de mama e/ou ovário, câncer colorretal, câncer gástrico, polipose adenomatosa familial, síndrome de Lynch, síndrome de Li-Fraumeni, neurofibromatose, esclerose tuberosa, melanoma, síndrome de Von Hippel-Lindau, retinoblastoma, neoplasia endócrina múltipla, anemia de Fanconi, entre outros.

Contém os genes APC, ATM, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, FANCA, FANCG, FANCC, FACND2, FANCB, FACD1 (BRCA2), FANCN (PALB2), FANCO (RAD51C) e FANCP (SLX4), MEN1, MEN2A, MLH1, MSH2, MSH6, MUTYH, PALB2, PMS2, PTCH1, PTEN, RAD51C, RAD51D, RB1, SMAD4, STK11, TP53, VHL, que possuem cobertura pela ANS

AIP, ALK, APC, ATM, AXIN2, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, BUB1B, CASR, CDC73, CDH1, CDK4, CDKN1B, CDKN1C, CDKN2A, CEBPA, CEP57, CHEK2, CTNNA1, CYLD, DDB2, DICER1, DIS3L2, DLST, EGFR, EPCAM, ERCC2, ERCC3, ERCC4, ERCC5, EXT1, EXT2, EZH2, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FH, FLCN, GATA2, GPC3, GREM1, HNF1A, HOXB13, HRAS, KIT, MAX, MEN1, MET, MITF, MLH1, MRE11, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NF2, NSD1, NTHL1, PALB2, PDGFRA, PHOX2B, PIK3CA, PMS1, PMS2, POLD1, POLE, POT1, PPM1D, PRF1, PRKAR1A, PTCH1, PTEN, RAD50, RAD51C, RAD51D, RB1, RECQL4, RET (MEN2A), RHBDF2, RUNX1, SBDS, SDHA, SDHAF2, SDHB, SDHC, SDHD, SLC25A11, SLX4, SMAD4, SMARCA4, SMARCB1, SMARCE1, STK11, SUFU, TERC, TERT, TMEM127, TP53, TSC1, TSC2, VHL, WRN, WT1, XPA, XPC, XRCC2

40503801

40 a 60 dias úteis

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