GENE
AKT1, APC, ATM, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EGFR, EPCAM, GREM1, HOXB13, MEN1, MITF, MLH1, MRE11A, MSH2, MSH6, MUTYH, NBN, NF1, PALB2, PIK3CA, PMS2, POLD1, POLE, PTEN, RAD50, RAD51, RAD51C, RAD51D, RB1, RECQL, RET, SMAD4, STK11, TP53, VHL e XRCC2 + Análise de CNVs
PARA QUE SERVE?
Avaliar as principais síndrome genéticas associadas ao câncer hereditário. Painel de 37 genes: APC, ATM, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EGFR, EPCAM, FANCC, FANCM, MEN1, MET, MLH1, MSH2, MSH3, MSH6, MUTYH, NBN, NTHL1, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, RECQL, RET, STK11, TP53.
MÉTODO
NGS
AMOSTRAS BIOLÓGICAS
Sangue Periférico (4 ml)
Saliva (1 ml)
ANTICOAGULANTE
EDTA (tampa roxa)
Kit coleta saliva
PRAZO
35 dias úteis
CÓDIGO MANTIS
BM083
CÓDIGO TUSS
40503801