- A
- Acral melanoma - Common cancer
-
MET
- Acute lymphoblastic leukaemia - Rare cancer
-
ABL1, ALK, CD19, CD20, DHFR, ERBB2, FGFR1, JAK2, KMT2A, XPO1
- Acute myeloid leukaemia - Rare cancer
-
ABL1, BRAF, CD33, ERBB2, FGFR1, FLT3, IDH1, IDH2, KIT, KMT2A, KRAS, NF1, NRAS, PTEN, PTPN11, RAD21, SF3B1, SMC3, SRSF2, STAG2, TP53, U2AF1
- Acute promyelocytic leukaemia - Rare cancer
-
XPO1
- Adenoid cystic carcinoma - Rare cancer
-
KIT, MYB, NOTCH1
- Aggressive fibromatosis - Rare cancer
-
APC, CTNNB1
- Ampullary carcinoma - Rare cancer
-
ERBB2
- Anal cancer - Rare cancer
-
HPV genotype
- Anaplastic astrocytoma - Rare cancer
-
IDH1, Mismatch repair, Tumour Mutational Burden
- Anaplastic ganglioglioma - Rare cancer
-
BRAF
- Anaplastic large cell lymphoma - Rare cancer
-
ALK, CD30
- Anaplastic pleomorphic xanthoastrocytoma - Rare cancer
-
RAF1
- Anaplastic thyroid cancer - Rare cancer
-
BRAF, MTOR, TSC2
- Appendiceal cancer - Rare cancer
-
GNAS, KRAS
- Appendiceal carcinoma - Rare cancer
-
KRAS
- Atypical teratoid rhabdoid tumor - Rare cancer
-
EZH2, RB1, SMARCB1
- B
- Basal cell carcinoma - Common cancer
-
GLI1, GLI2, PTCH1, SMO, SUFU
- Biliary tract cancer - Rare cancer
-
BRAF, CDKN2A, ERBB2
- Biliary tract cancers - Rare cancer
-
BRAF, CD274, ERBB2
- Bladder cancer - Common cancer
-
ERBB2
- Blastic plasmacytoid dendritic cell neoplasm - Rare cancer
-
CD123
- Breast adenocarcinoma - Common cancer
-
KRAS
- Breast cancer - Common cancer
-
AKT1, AKT3, ALK, AR, AR+ESR1, ARID1A, ATM, BARD1, BCL2, BCL6, BRCA1, BRCA1+ERBB2, BRCA2, CCNE1, CDH1, CDK4, CDK6, CHEK2, EIF4EBP1, ERBB2, ERBB2+ERBB3, ERBB2+ESR1, ERBB3, ESR1, ESR1+CCNE1, ESR1+ERBB2, ESR1+ERBB2+PIK3CA, ESR1+MDM2, ESR1+PIK3CA, ESR1+TP53, FAM175A, FGFR1, FGFR2, HRAS, Homologous Recombination Deficiency Score, Intrinsic subtype, KAT6A, KRAS+NRAS+BRAF, MAP3K1+PIK3CA, MRE11A, MTOR, NRAS, NRG1, PALB2, PAXIP1, PGR, PIK3CA, PIK3CA+ESR1+ERBB2, PIK3CA+FGFR1, PIK3CA+FGFR2, PTEN, PTEN+ERBB2, RAD50, RAD51C, RB1, RIF1, SPEN, TACSTD2, TOP1, TP53BP1, Tumour Mutational Burden, XRCC2
- Breast secretory carcinoma - Common cancer
-
NTRK1, NTRK2, NTRK3
- C
- Cancer of unknown primary - Rare cancer
-
FGFR2, KRAS, NRAS, Tumour Mutational Burden
- Central nervous system cancer - Rare cancer
-
NTRK1, NTRK2, NTRK3
- Cervical cancer - Uncommon cancer
-
CD274, EGFR, ERBB2, ERCC1, FGFR2, FGFR2 , FGFR3, HPV genotype, NECTIN4, Tumour Mutational Burden
- Cholangiocarcinoma - Rare cancer
-
BAP1, BRAF, CDKN2A, ERBB2, ERRFI1, FGFR2, FGFR3, IDH1, IDH2, KRAS, MDM2+TP53, NRAS, NRG1
- Chondrosarcoma - Rare cancer
-
IDH1, IDH2
- Chordoma - Rare cancer
-
SMARCB1
- Chronic eosinophilic leukaemia - Rare cancer
-
JAK2, PDGFRA
- Chronic lymphocytic leukaemia - Rare cancer
-
ATM, ATR, BCL2, CD20, TP53
- Chronic myelogenous leukaemia - Rare cancer
-
ABL1, BAP1, LZTR1, NF1, PTPN11, WT1, XPO1
- Chronic myelomonocytic leukaemia - Rare cancer
-
SF3B1, SRSF2
- Clear cell renal cell carcinoma - Rare cancer
-
BAP1
- Colon adenocarcinoma - Common cancer
-
KRAS
- Colorectal adenocarcinoma - Common cancer
-
ALK, APC, APC+PIK3CA, ARID1A, ATM, ATR, B2M, BRAF, BRAF+KRAS, BRAF+MAP2K1, BRAF+MET, BRAF+NRAS, Consensus molecular subtype, EGFR, ERBB2, ERBB2+KRAS, ERBB3, FBXW7, FLT3, HRAS, IRS2, IRS2+BRAF, IRS2+KRAS, Immunoscore IC, KRAS, KRAS+ERBB3, KRAS+Microsatellite Instability, KRAS+Mismatch repair, KRAS+NRAS, MAP2K1, MET, MGMT, MLH1, MYB, MYC, Microsatellite Instability, Microsatellite instability+Mismatch repair, Mismatch repair, NF1, NRAS, PIK3CA, PIK3R2, POLD1, POLE, PTEN, RET, RNF43, ROS1, RSPO1, TP53, TP53+KRAS, Tumour Mutational Burden, Tumour Mutational Burden+Microsatellite, Tumour Mutational Burden+Mismatch repair
- Colorectal cancer - Common cancer
-
CEACAM5, EGFR, ERBB2, ERBB2+KRAS, FGFR1, KRAS, POLD1, POLE
- Colorectal neuroendocrine carcinoma - Common cancer
-
BRAF
- Cutaneous T-cell lymphoma - Rare cancer
-
CCR4, CD30
- E
- Endometrial cancer - Uncommon cancer
-
AKT1, ARID1A, BRAF, CCNE1, ERBB2, ESR1, FGFR1, FGFR2, FGFR2 , FGFR3, Homologous Recombination Deficiency Score, KRAS, MCL1, Microsatellite Instability, Microsatellite instability+Mismatch repair, Mismatch repair, PGR, PIK3CA, PIK3R1, PTEN, TP53, Tumour Mutational Burden
- Endometrial carcinoma - Uncommon cancer
-
KRAS, MET
- Endometrioid endometrial cancer - Uncommon cancer
-
ERBB2, ESR1, PGR
- Ependymoma - Rare cancer
-
NF2, NTRK2
- Epithelial-myoepithelial carcinoma - Rare cancer
-
HRAS
- Epithelioid haemangioendothelioma - Rare cancer
-
CAMTA1, IDH2, WWTR1, YAP1
- Epithelioid hemangioendothelioma - Rare cancer
-
IDH1, IDH2
- Epithelioid sarcoma - Rare cancer
-
EZH2, RB1, SMARCB1
- Erdheim-Chester disease - Rare cancer
-
BRAF
- Ewing sarcoma - Rare cancer
-
FLI1
- Extramammary Paget’s disease - Rare cancer
-
ERBB2, ERBB2+PTEN, ERBB3, MET
- Extrapulmonary neuroendocrine carcinoma - Rare cancer
-
DLL3
- G
- Gallbladder cancer - Common cancer
-
ATM, CDKN2A, ERBB2, MTAP
- Gastric cancer - Common cancer
-
ARID1A, BRAF, CCND1, CD274, CLDN18, CLDN18+ERBB2, CLDN6, EGFR, ERBB2, ERBB2+CD274, ERBB3, FGFR2, FGFR3, HGF, KRAS, MET, Microsatellite Instability, PIK3CA, PTEN, RICTOR, TP53, Tumour Mutational Burden
- Gastroesophageal junction adenocarcinoma - Common cancer
-
CCND1, CD274, CLDN18, CLDN18+ERBB2, EGFR, ERBB2, ERBB2+CD274, FGFR2, KRAS, MET, Microsatellite Instability, PIK3CA, PTEN, TP53
- Gastrointestinal neuroendocrine carcinoma - Rare cancer
-
BRAF
- Gastrointestinal stromal tumour - Rare cancer
-
CDKN2A, KIT, NF1+KIT, PDGFRA
- Gastrooesophageal carcinoma - Uncommon cancer
-
Tumour Mutational Burden
- Glioblastoma - Rare cancer
-
ABL1, ATM, BRAF, CDK4, CDKN2A, EGFR, FGFR1, FGFR3, IDH1, IDH2, KIT, MDM2+TP53+IDH1, MET, MGMT, MSH2, Mismatch repair, NF1, NOTCH2, PIK3CA, PIK3R1, PMS2, PTEN, Tumour Mutational Burden
- Glioma - Rare cancer
-
AR, BRAF, EGFR, IDH1, IDH2
- Gliomas - Rare cancer
-
BRAF
- Glioneuronal tumour - Rare cancer
-
BRAF
- Granulosa cell tumour - Rare cancer
-
PGR
- H
- H3K27M-mutant glioma - Rare cancer
-
H3F3A
- Hairy cell leukaemia - Rare cancer
-
BRAF
- Head and neck squamous cell carcinoma - Rare cancer
-
AKT1, BRCA1, CD274, EGFR, ERBB4, FANCC, HPV genotype, HRAS, Human Papillomavirus Status, MAPK1, MET, RB1
- Hemangioblastoma - Rare cancer
-
VHL
- Hepatobiliary cancers - Rare cancer
-
Tumour Mutational Burden
- Hepatocellular carcinoma - Rare cancer
-
CD274, CRKL, FGF19, FGFR4, GPC3
- High-grade glioma - Rare cancer
-
BRAF
- High-grade gliomas - Rare cancer
-
ALK, BRAF, H3F3A, IDH1, KRAS, Mismatch repair, NF1, NTRK1, NTRK2, NTRK3, Tumour Mutational Burden
- High-grade well-differentiated neuroendocrine tumour - Rare cancer
-
SEZ6
- Histiocytic sarcoma - Rare cancer
-
MET
- Histiocytosis - Rare cancer
-
ALK, ARAF, BRAF, KRAS, MAP2K1, MAP2K2, NRAS, PTPN11, RAF1
- Hodgkin’s lymphoma - Rare cancer
-
CD20, CD30
- HPV16-positive cancers - Rare cancer
-
HPV genotype
- L
- Langerhans cell histiocytosis - Rare cancer
-
BRAF
- Langerhans cell sarcoma - Rare cancer
-
RASA1
- Liposarcoma - Rare cancer
-
FRS2
- Liquid cancers - Rare cancer
-
BCL2, IDH2, JAK1, JAK2, MYC, MYCN, SF3B1, SLC1A5, TP53
- Low-grade glioma - Rare cancer
-
BRAF, CDKN2A, EGFR, IDH1, IDH2
- Low-grade gliomas - Rare cancer
-
BRAF, IDH1, IDH2, NTRK1, NTRK2, NTRK3, RAF1
- Low-grade serous ovarian cancer - Uncommon cancer
-
BRAF, KRAS, MAP2K1
- Low-grade serous ovarian carcinoma - Uncommon cancer
-
PGR
- Low-grade spindle cell neoplasm - Rare cancer
-
BRAF, CDKN2A
- Lung adenocarcinoma - Common cancer
-
BRAF, ERBB2, FGFR1, KRAS, MET, RET
- Lung squamous cell carcinoma - Common cancer
-
ATM, ATR, BRCA1, BRCA2, CCND1, CCND2, CCND3, CDK4, CDK6, CHEK1, ERBB2, FANCC, FANCM, FGFR1, FGFR2, FGFR3, MET, NRG1, PALB2, PIK3CA, TP63
- M
- Malignant peripheral nerve sheath tumor - Rare cancer
-
MTAP, NF1, NF1+MET, NF1+SUZ12
- Malignant peripheral nerve sheath tumour - Rare cancer
-
CD274
- Malignant rhabdoid tumor - Rare cancer
-
SMARCA4
- Mammary analogue secretory carcinoma - Rare cancer
-
NTRK1, NTRK2, NTRK3
- Mantle cell lymphoma - Rare cancer
-
CD20
- Marginal zone lymphoma - Rare cancer
-
CD20
- Mastocytosis - Rare cancer
-
KIT, PDGFRA
- Medullary thyroid cancer - Rare cancer
-
BRAF, FGFR1, MET, RET
- Medulloblastoma - Rare cancer
-
NTRK3, PTCH1, SMO
- Melanoma - Common cancer
-
ARID2, B2M, BRAF, BRCA2, BRD7, CTNNB1+KIT, ERBB4, FBXW7, HLA-A+PMEL, HLA-A2, HLA-A2+PRAME, JAK1, JAK2, KIT, KRAS, MAP2K1, MAP2K1+BRAF, MAP2K2, MAPK1, MAPK3, NF1, NRAS, PBRM1, RAF1
- Meningioma - Rare cancer
-
CDKN2A, NF2
- Merkel cell carcinoma - Rare cancer
-
TP53
- Mesothelioma - Rare cancer
-
BAP1, BRCA1, CDKN2A, ERCC1, MRE11A, MSLN, MTAP, NF2
- Metaplastic breast carcinoma - Common cancer
-
PIK3CA
- Mixed phenotype acute leukaemia - Rare cancer
-
KMT2A
- Multiple myeloma - Rare cancer
-
BRAF, CD38, KDM6A, SLAMF7, TNFRSF17
- Mycosis fungoides - Rare cancer
-
CCR4
- Myelodysplastic/myeloproliferative diseases - Rare cancer
-
FGFR1, PDGFRA, PDGFRB
- Myelodysplastic syndrome - Rare cancer
-
IDH2, RAD21, SF3B1, SMC3, SRSF2, STAG2, TP53
- Myelofibrosis - Rare cancer
-
JAK2
- Myeloproliferative diseases - Rare cancer
-
FGFR1
- Myxoid liposarcoma - Rare cancer
-
CTAG1B
- N
- Nasopharyngeal carcinoma - Rare cancer
-
CD276
- Neuroblastoma - Rare cancer
-
ALK, ATRX, BARD1, DLK1, MYC, MYCN, NRAS
- Neuroendocrine carcinoma - Rare cancer
-
BRAF, DLL3, SEZ6, Tumour Mutational Burden
- Neuroendocrine tumour - Rare cancer
-
SSTR2, Tumour Mutational Burden
- Non-clear cell renal cell carcinoma - Rare cancer
-
SETD2
- Non-Hodgkin’s lymphoma - Common cancer
-
CD20, EZH2
- Non-melanoma skin cancer - Common cancer
-
Tumour Mutational Burden
- Nonseminoma - Rare cancer
-
Chromosome
- Non-small cell lung cancer - Common cancer
-
ALK, ARAF, ATM, BCL2L11, BRAF, BRAF+EGFR, BRAF+KRAS, BRAF+MAP2K1, BRAF+NRAS, BRAF+PTEN, BRCA1, BRCA2, CD274, CD274+EGFR+ALK, CD276, CDKN2A, CEACAM5, CLDN6, CRKL, DNMT3A, EGFR, EGFR+ALK, EGFR+BRAF, EGFR+CD274, EGFR+EGFR, EGFR+ERBB2, EGFR+MET, EGFR+MET+ALK, EGFR+MET+BRAF, EGFR+MET+KRAS, EGFR+RB1, EGFR+RBM10, EGFR+RET, EGFR+ROS1, EGFR+TP53, ERBB2, ERBB3, ERBB4, FANCD2, FBXW7, FGFR2, FGFR3, GNAS, KEAP1, KEAP1+KRAS, KRAS, KRAS+ERBB3, KRAS+MET, KRAS+NRAS+BRAF, KRAS+STK11, KRAS+TP53, Loss-of-heterozygosity score, MAP2K1, MET, MET+TP53, MRAS, MTAP, NF1, NOTCH3, NRAS, NRG1, PIK3CA, RASA1, RB1, RBM10, RET, ROS1, ROS1+MET, SMARCA4, STK11, STK11+KRAS, TOP1, Tumour Mutational Burden
- Non-small cell lung carcinoma - Common cancer
-
CD274
- Non-vestibular schwannoma - Rare cancer
-
NF2
- NUT carcinoma - Rare cancer
-
BRD3, BRD4, NUTM1
- O
- Oesophageal adenocarcinoma - Uncommon cancer
-
CD274, ERBB2, FGFR2, KRAS, MET
- Oesophageal cancer - Uncommon cancer
-
CD274, NECTIN4
- Oesophageal squamous cell carcinoma - Uncommon cancer
-
CD274, LGALS1, NTRK1
- Osteosarcoma - Rare cancer
-
Mutational signature
- Ovarian cancer - Uncommon cancer
-
ARID1A, ATM, BRAF, BRCA1, BRCA1+BRCA2, BRCA2, CCNE1, CD274, CDH6, CDK12, CLDN6, EMSY, ERBB2, ERCC1, FGFR2, FOLR1, Homologous Recombination Deficiency Score, KRAS, KRAS+NRAS+BRAF, Loss-of-heterozygosity score, MSLN, NRG1, PALB2, RAD50, RAD51C, RAD51D, ROS1, SETD2
- Ovarian clear cell carcinoma - Uncommon cancer
-
ARID1A
- Ovarian mucinous carcinoma - Uncommon cancer
-
ERBB2
- Ovarian small cell carcinoma - Uncommon cancer
-
SMARCA2, SMARCA2+SMARCA4, SMARCA4
- P
- Paediatric low grade gliomas - Rare cancer
-
BRAF
- Pancreatic acinar cell carcinoma - Rare cancer
-
KRAS, RAF1
- Pancreatic adenocarcinoma - Uncommon cancer
-
ARID1A, ARID1B, ATM, BRAF, BRCA1, BRCA2, CCL11, CDKN2A, CLDN18, EGFR, ERBB2, FANCD2, FANCG, FGFR1, FGFR2, KDM6A, KRAS, MDM2+TP53, Mismatch repair, NOTCH3, NRG1, NTRK1, PALB2, PBRM1, PTEN, RAD51C, RNF43, ROS1, SF3B1, SMARCA4, SMARCB1, STK11, TP53
- Pancreatic cancer - Rare cancer
-
BRCA1, BRCA2, PALB2, RAD51C, RAD51D, Tumour Mutational Burden
- Pancreatic neuroendocrine tumour - Rare cancer
-
MGMT, SSTR2, VHL
- Papillary craniopharyngioma - Rare cancer
-
BRAF
- Papillary renal cell carcinoma - Rare cancer
-
FH, HGF, MET, NF2
- Papillary thyroid cancer - Rare cancer
-
BRAF, ROS1
- Paraganglioma - Rare cancer
-
EPAS1, RET, SDHA, SDHB
- Penile cancer - Rare cancer
-
EGFR
- Peritoneal mucinous carcinomatosis - Uncommon cancer
-
GNAS
- Peritoneal serous carcinoma - Uncommon cancer
-
BRCA1, BRCA2, FOLR1, Homologous Recombination Deficiency Score, Loss-of-heterozygosity score
- Perivascular epithelioid cell tumour - Rare cancer
-
TSC1, TSC2
- Phaeochromocytoma - Rare cancer
-
RET, SDHA, SDHB
- Pilocytic astrocytoma - Rare cancer
-
RAF1
- Pituitary adenoma - Rare cancer
-
STK11
- Polycythemia vera - Rare cancer
-
EPAS1, JAK2
- Prostate cancer - Common cancer
-
AR, ATM, AURKA, BARD1, BRCA1, BRCA2, BRIP1, CD276, CDK12, CHEK1, CHEK2, ERBB3, FANCA, FANCG, FANCI, FANCL, FGFR2, MYCN, Microsatellite Instability, Mismatch repair, NBN, PALB2, PIK3R1, PPP2R2A, PSMA, PTEN, RAD51B, RAD51C, RAD51D, RAD54L, RB1, STEAP1, TP53, TP53+RB1, Tumour Mutational Burden, Tumour Mutational Burden+Microsatellite Instability, Tumour Mutational Burden+Mismatch repair
- Prostate small cell carcinoma - Common cancer
-
ALK, DLL3
- R
- Renal cell carcinoma - Uncommon cancer
-
ALK, CDH6, FLCN, MTOR, PBRM1, PTEN, TSC1, TSC2, VHL
- Rhabdoid tumors - Rare cancer
-
SMARCB1
- Rhabdomyosarcoma - Rare cancer
-
CDK4, KRAS, NRAS
- Round cell liposarcoma - Rare cancer
-
CTAG1B
- S
- Salivary duct carcinoma - Rare cancer
-
HRAS
- Salivary gland cancer - Rare cancer
-
ERBB2
- Salivary gland cancers - Rare cancer
-
AR, BRAF, ERBB2, HRAS, Tumour Mutational Burden
- Sarcoma - Rare cancer
-
BRAF, NF2, PDGFRA, Tumour Mutational Burden
- Sarcomatoid renal cell carcinoma - Rare cancer
-
NF2
- Seminoma - Rare cancer
-
Chromosome
- Small-cell lung cancer - Common cancer
-
BCL2, CD276, CHEK1, DLL3, IRS2, MET, MYC, MYCL, MYCN, POU2F3, SEZ6, Tumour Mutational Burden
- Small intestine adenocarcinoma - Rare cancer
-
BRAF
- SMARCA4-deficient thoracic sarcoma - Rare cancer
-
SMARCA4
- Soft tissue sarcomas - Rare cancer
-
PDGFRA
- Solid tumour - Rare cancer
-
AKT1, ATM, ATR, BRAF, BRCA1, BRCA2, BRIP1, CCND1, CCND2, CCND3, CD8, CDK4, CDK6, CDKN2A, CHEK2, EGFR, ERBB2, ERBB3, FGFR1, FGFR2, FGFR3, GNA11, GNAQ, HRAS, KRAS, MET, MTAP, NF1, NRAS, PTEN, RAD50, RET, ROS1, SEZ6, TP53
- Solid tumours - Rare cancer
-
AKT1, AKT2, ALK, AR, ARAF, ARID1A, ARID2, ATM, ATM+TP53, ATRX, BAP1, BARD1, BCL2, BCL2L1, BRAF, BRCA1, BRCA2, BRD4, CCND1, CCND2, CCND3, CCNE1, CD274, CD276, CDK12, CDK4, CDK6, CDKN2A, CDKN2A+MTAP, CEACAM5, CHEK1, CLDN18, CLDN6, DAXX, EGFR, EGFR+ERBB3, EGFR+ERRFI1, EPHA7, ERBB2, ERBB2+KRAS, ERBB3, EZH2, F3, FANCA, FAT1, FBXW7, FGFR1, FGFR2, FGFR3, FGFR4, FOLR1, GNA11, GNAQ, Globo H, HLA-A, HRAS, IDH1, IDH2, KIT, KRAS, LRP1B, MAP2K1, MAP2K4, MAP3K1, MCL1, MDM2, MET, MET+KRAS, MGMT, MLH1, MSH2, MSH6, MSLN, MTAP, MTORC1, MUC1, MYB, MYC, MYCN, Microsatellite Instability, Mismatch repair, NECTIN4, NF1, NF2, NOTCH1, NRAS, NRG1, NTRK1, NTRK2, NTRK3, PBRM1, PDCD1LG2, PIK3CA, PIK3R1, PMS2, POLD1, POLE, PRKCA, PRKCB, PRKDC, PTCH1, PTEN, PTPN11, RAC1, RAD51C, RAD51D, RAF1, RB1, RET, RIT1, RNF43, ROS1, SF3B1, SLC1A5, SLC39A6, SLX4, SMARCA4, SMARCB1, SMO, SUZ12, TACSTD2, TP53, TSC1, TSC2, Tumour Mutational Burden, VCTN1
- Solitary fibrous tumour - Rare cancer
-
FGFR1, FGFR2
- Somatostatinoma - Rare cancer
-
EPAS1
- Spindle cell sarcoma - Rare cancer
-
RAF1
- Subependymal giant cell astrocytoma - Rare cancer
-
TSC1, TSC2
- Synovial sarcoma - Rare cancer
-
CTAG1B, SS18
- Sézary syndrome - Rare cancer
-
CCR4
- T
- T-cell acute lymphoblastic leukaemia - Rare cancer
-
ABL1
- Tenosynovial giant cell tumor - Rare cancer
-
CSF1
- Testicular cancer - Rare cancer
-
CLDN6
- Thymic carcinoma - Rare cancer
-
CD274, KIT, PBRM1
- Thymic neuroendocrine carcinoma - Rare cancer
-
KIT
- Thymoma - Rare cancer
-
PBRM1
- Thyroid cancer - Rare cancer
-
EIF1AX, EIF1AX+NRAS, RET, Tumour Mutational Burden
- Triple-negative breast cancer - Common cancer
-
AKT1, AR, ATM, BRAF, BRCA1, BRCA1+BRCA2, BRCA2, CCNE1, CD274, CDK12, DAXX, EGFR, ERBB2, ESR1+ERBB2, MET, Molecular subtype, NECTIN4, NF1, NOTCH2, PIK3CA, PTEN, RAD51, RB1, TACSTD2, Tumour microenvironment
- Type 1 neurofibromatosis - Rare cancer
-
NF1
- Type 2 neurofibromatosis - Rare cancer
-
NF2
- U
- Urothelial carcinoma - Common cancer
-
ARID1A, ATM, BARD1, BRCA1, BRCA2, BRIP1, CD274, CDK12, CDKN2A, CXCL13, EGFR+ERBB3, ERBB2, ERBB3, ERCC2, FGFR1, FGFR2, FGFR3, HRAS, KMT2C, MTOR, NECTIN4, NF2, RAD51C, TSC1
- Uterine carcinosarcoma - Rare cancer
-
ERBB2, POLE
- Uterine leiomyosarcoma - Rare cancer
-
BRCA2, BRCA2+PTEN, RAD51
- Uterine serous carcinoma - Rare cancer
-
BRIP1, ERBB2, Homologous Recombination Deficiency Score, TP53
- Uveal melanoma - Common cancer
-
BAP1, GNA11, GNAQ, HLA-A+PMEL, HLA-A2
include('common-tail.php') ;
?>