OncoSeq® C

OncoSeq® C offers a comprehensive range of molecular genetic
analysis reports that help identify genetic variations that could be
associated with cancer development.

The OncoSeq® C reports are only generated by accredited and approved
partner laboratories that follow strict international quality guidelines.

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OncoSeq® C Reports

OncoSeq®  C offers comprehensive clinical reports with clinically relevant findings for a variety of hereditary cancers.

Report Gene Cancer(s)
Oncoseq C Breast Covers 4304 hotspots over 20 genes: ATM, BARD1, BRCA1, BRCA2, BRIP1, C11orf65, CDH1, CHEK2, MUTYH, NBN, PALB2, PTEN, RAD50, RAD51C, RAD51D, RAD51L3-RFFL, TH2-LCR, TH2LCRR, TOE1, TP53,
  • Bilateral Breast Cancer
  • BRCA2-Related Disorders
  • Breast adenocarcinoma
  • Breast carcinoma
  • Breast lobular carcinoma
  • Breast neoplasm
  • BRIP1-associated familial cancer predisposition
  • Cowden syndrome
  • Ductal carcinoma in situ
  • Familial breast and ovarian cancer
  • Hereditary breast ovarian cancer syndrome
  • Li-Fraumeni syndrome
  • Malignant tumor of breast
  • Neoplasm of ovary
  • Neoplasm of uterine cervix
  • Ovarian carcinoma
  • Ovarian serous cystadenocarcinoma
  • Ovarian serous surface papillary adenocarcinoma
  • PALB2-Related Disorders
    •  .... Read More
Oncoseq C Colon Covers 1800 hotspots over 10 genes; APC, MLH1, MSH2, MSH6, MUTYH, PMS2, PTEN, STK11, TOE1, TP53
  • Adenomatous colonic polyposis
  • APC-related attenuated familial adenomatous polyposis
  • Colorectal cancer
  • Cowden syndrome
  • Endometrial cancer
  • Familial adenomatous polyposis 1
  • Hereditary nonpolyposis colon cancer
  • Hereditary nonpolyposis colorectal carcinoma
  • Li-Fraumeni-like syndrome
  • Li-Fraumeni syndrome
  • Lynch-like syndrome
  • Lynch syndrome
  • Mismatch repair cancer syndrome
  • Muir-Torré syndrome
  • Peutz-Jeghers syndrome
  • PTEN hamartoma tumor syndromes
  • Turcot syndrome
    •  .... Read More
Oncoseq C Prostate Covers 5137 hotspots over 13 genes; ATM, BRCA1, BRCA2, C11orf65, CHEK2, MLH1, MSH2, MSH6, PALB2, PMS2, RAD51D, RAD51L3-RFFL, TP53
  • Adrenal cortex carcinoma
  • Adrenocortical carcinoma, hereditary
  • BAP1-related tumor predisposition syndrome
  • BRCA2-Related Disorders
  • CHEK2-Related Cancer Susceptibility
  • Hereditary cancer-predisposing syndrome
  • Li-Fraumeni syndrome
  • Lymphoma
  • Lynch syndrome
  • Malignant tumor of prostate
  • Metastatic Prostate Small Cell Carcinoma
  • Mismatch repair cancer syndrome
  • PALB2-Related Disorders
  • Cancer of the pancreas
  • Prostate adenocarcinoma
  • Prostate cancer, somatic
  • Prostate cancer, susceptibility to
  • Sarcoma
  • Wilms tumor 1
    •  .... Read More
Oncoseq C Complete Covers 6920 hotspots over 125 genes; ALK, AOPEP, APC, ATM, BAP1, BARD1, BIVM-ERCC5, BLM, BMPR1A, BRAF, BRCA1, BRCA2, BRIP1, C11orf65, CBL, CDC73, CDH1, CDK4, CDKN1B, CDKN2A, CHEK2, CTNNA1, DDX41, DICER1, DIS3L2, DKC1, EGFR, ELANE, ERCC2, ERCC3, ERCC4, ERCC5, EXT1, EZH2, FANCA, FANCC, FANCD2, FANCF, FANCG, FANCI, FANCM, FH, FLCN, GALNT12, GPC3, HNF1A, HRAS, KIF1B, KIT, KRAS, LOC107303338, LOC107303340, LOC111811965, LRRC56, LZTR1, MAP2K1, MAP2K2, MAX, MEN1, MET, MITF, MLH1, MLH3, MRE11, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NF2, NRAS, NSD1, PALB2, PMS2, POLD1, POLE, PRF1, PRKAR1A, PTCH1, PTEN, PTPN11, RAD50, RAD51C, RAD51D, RAD51L3-RFFL, RAF1, RB1, RECQL4, RECQL, RET, RIT1, RUNX1, SBDS, SDHA, SDHAF2, SDHB, SDHC, SDHD, SHOC2, SLX4, SMAD4, SMARCA4, SMARCB1, SMARCE1, SOS1, SOS2, SPRED1, STK11, SUFU, TERT, TH2-LCR, TH2LCRR, TINF2, TMEM127, TOE1, TP53, TSC1, TSC2, VHL, WRN, WT1, XPC, XRCC2, ZNF276 .... Read More
  • Bone osteosarcoma
  • Breast and/or ovarian cancer
  • Breast lobular carcinoma
  • Cancer of the pancreas
  • Carcinoma of esophagus
  • CHEK2-Related Cancer Susceptibility
  • Clear cell carcinoma of kidney
  • Cowden syndrome
  • Endometrial cancer
  • Familial adenomatous polyposis 1
  • Familial medullary thyroid carcinoma
  • Gardner syndrome
  • Hereditary diffuse gastric adenocarcinoma
  • Hereditary leiomyomatosis and renal cell cancer
  • Hereditary nonpolyposis colon cancer
  • Hereditary pheochromocytoma-paraganglioma
  • Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome
  • Li-Fraumeni-like syndrome
  • Lung adenocarcinoma
  • Lynch-like syndrome
  • Lynch syndrome
  • Medulloblastoma
  • Muir-Torré syndrome
  • Multiple endocrine neoplasia
  • MUTYH-related attenuated familial adenomatous polyposis
  • Non-small cell lung carcinoma
  • PALB2-Related Disorders
  • Peutz-Jeghers syndrome
  • PTEN hamartoma tumor syndrome
  • Retinoblastoma
  • Squamous cell carcinoma of the head and neck
  • Von Hippel-Lindau syndrome
  • Wilms tumor 1
    •  .... Read More

Who should get OncoSeq® C Screening done?

  • An individual who is diagnosed with the cancer
  • When there is a family history of cancer
  • When there is an increased risk of cancer
  • When you are worried about the risk of cancer

Sample Requirement

  • Saliva or Buccal Swab
How it Work

For more details about each panel and a complete list of syndromes, please contact our partners