Compendium of Cancer Genome Aberrations

Volunteer Assignments and Opportunities: Difference between revisions

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!'''Date of Last Editor Review'''
!'''Date of Last Editor Review'''
!'''Notes'''
!'''Notes'''
|- |Astrocytoma, IDH-mutant||Disease||
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|Oligodendroglioma, IDH-mutant and 1p/19q-codeleted||Disease||
|Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted||Disease||
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Line 2,598: Line 2,590:
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|Glioblastoma, IDH-wildtype||Disease||
|Glioblastoma, IDH-Wildtype||Disease||
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Line 2,607: Line 2,599:
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|Diffuse astrocytoma, MYB- or MYBL1-altered||Disease||
|Diffuse Astrocytoma, MYB- or MYBL1-Altered||Disease||
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Line 2,616: Line 2,608:
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|Angiocentric glioma||Disease||
|Angiocentric Glioma||Disease||
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Line 2,625: Line 2,617:
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|Polymorphous low-grade neuroepithelial tumour of the young||Disease||
|Polymorphous Low-Grade Neuroepithelial Tumour of the Young||Disease||
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Line 2,634: Line 2,626:
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|Diffuse low-grade glioma, MAPK pathway-altered||Disease||
|Diffuse Low-Grade Glioma, MAPK Pathway-Altered||Disease||
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Line 2,643: Line 2,635:
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|Diffuse midline glioma, H3 K27-altered||Disease||
|Diffuse Midline Glioma, H3 K27-Altered||Disease||
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Line 2,652: Line 2,644:
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|Diffuse hemispheric glioma, H3 G34-mutant||Disease||
|Diffuse Hemispheric Glioma, H3 G34-Mutant||Disease||
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Line 2,661: Line 2,653:
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|Diffuse paediatric-type high-grade glioma, H3-wildtype and IDH-wildtype||Disease||
|Diffuse Paediatric-Type High-Grade Glioma, H3-Wildtype and IDH-Wildtype||Disease||
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Line 2,670: Line 2,662:
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|Infant-type hemispheric glioma||Disease||
|Infant-Type Hemispheric  Glioma||Disease||
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Line 2,679: Line 2,671:
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|Pilocytic astrocytoma||Disease||
|Pilocytic Astrocytoma||Disease||
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Line 2,688: Line 2,680:
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|High-grade astrocytoma with piloid features||Disease||
|High-Grade Astrocytoma with Piloid Features||Disease||
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Line 2,697: Line 2,689:
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|Pleomorphic xanthoastrocytoma||Disease||
|Pleomorphic Xanthoastrocytoma||Disease||
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Line 2,706: Line 2,698:
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|Subependymal giant cell astrocytoma||Disease||
|Subependymal Giant Cell Astrocytoma||Disease||
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Line 2,715: Line 2,707:
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|Chordoid glioma||Disease||
|Chordoid Glioma||Disease||
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Line 2,724: Line 2,716:
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|Astroblastoma, MN1-altered||Disease||
|Astroblastoma, MN1-Altered||Disease||
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Line 2,751: Line 2,743:
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|Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma||Disease||
|Desmoplastic Infantile  Ganglioglioma/Desmoplastic Infantile Astrocytoma||Disease||
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Line 2,760: Line 2,752:
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|Dysembryoplastic neuroepithelial tumour||Disease||
|Dysembryoplastic Neuroepithelial Tumour||Disease||
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Line 2,769: Line 2,761:
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|Diffuse glioneuronal tumour with oligodendroglioma-like features and nuclear clusters||Disease||
|Diffuse Glioneuronal Tumour with Oligodendroglioma-Like Features and Nuclear Clusters||Disease||
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Line 2,778: Line 2,770:
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|Papillary glioneuronal tumour||Disease||
|Papillary Glioneuronal Tumour||Disease||
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Line 2,787: Line 2,779:
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|Rosette-forming glioneuronal tumour||Disease||
|Rosette-Forming Glioneuronal Tumour||Disease||
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Line 2,796: Line 2,788:
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|Myxoid glioneuronal tumour||Disease||
|Myxoid Glioneuronal Tumour||Disease||
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Line 2,805: Line 2,797:
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|Diffuse leptomeningeal glioneuronal tumour||Disease||
|Diffuse Lptomeningeal Glioneuronal Tumour||Disease||
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Line 2,814: Line 2,806:
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|Multinodular and vacuolating neuronal tumour||Disease||
|Multinodular and Vacuolating Neuronal Tumour||Disease||
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Line 2,823: Line 2,815:
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|Dysplastic cerebellar gangliocytoma (Lhermitte-Duclos disease)||Disease||
|Dysplastic Cerebellar Gangliocytoma (Lhermitte-Duclos Disease)||Disease||
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Line 2,832: Line 2,824:
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|Central neurocytoma||Disease||
|Central Neurocytoma||Disease||
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Line 2,841: Line 2,833:
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|Extraventricular neurocytoma||Disease||
|Extraventricular Neurocytoma||Disease||
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Line 2,850: Line 2,842:
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|Cerebellar liponeurocytoma||Disease||
|Cerebellar Liponeurocytoma||Disease||
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Line 2,859: Line 2,851:
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|Supratentorial ependymoma||Disease||
|Supratentorial Ependymoma||Disease||
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Line 2,868: Line 2,860:
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|Supratentorial ependymoma, ZFTA fusion-positive||Disease||
|Supratentorial Ependymoma, ZFTA Fusion-Positive||Disease||
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Line 2,877: Line 2,869:
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|Supratentorial ependymoma, YAP1 fusion-positive||Disease||
|Supratentorial Ependymoma, YAP1 Fusion-Positive||Disease||
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Line 2,886: Line 2,878:
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|Posterior fossa ependymoma||Disease||
|Posterior Fossa Ependymoma||Disease||
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Line 2,895: Line 2,887:
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|Posterior fossa group A (PFA) ependymoma||Disease||
|Posterior Fossa Group A (PFA) Ependymoma||Disease||
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Line 2,904: Line 2,896:
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|Posterior fossa group B (PFB) ependymoma||Disease||
|Posterior Fossa Group B (PFB) Ependymoma||Disease||
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Line 2,913: Line 2,905:
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|Spinal ependymoma||Disease||
|Spinal Ependymoma||Disease||
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Line 2,922: Line 2,914:
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|Spinal ependymoma, MYCN-amplified||Disease||
|Spinal Ependymoma, MYCN-Amplified||Disease||
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Line 2,931: Line 2,923:
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|Myxopapillary ependymoma||Disease||
|Myxopapillary Ependymoma||Disease||
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Line 2,949: Line 2,941:
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|Choroid plexus papilloma||Disease||
|Choroid Plexus Papilloma||Disease||
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Line 2,958: Line 2,950:
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|Atypical choroid plexus papilloma||Disease||
|Atypical Choroid Plexus Papilloma||Disease||
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Line 2,967: Line 2,959:
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|Choroid plexus carcinoma||Disease||
|Choroid Plexus Carcinoma||Disease||
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Line 2,976: Line 2,968:
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|Medulloblastoma, WNT-activated||Disease||
|Medulloblastoma, WNT-Activated||Disease||
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Line 2,985: Line 2,977:
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|Medulloblastoma, SHH-activated and TP53-wildtype||Disease||
|Medulloblastoma, SHH-Activated and TP53-Wildtype||Disease||
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Line 2,994: Line 2,986:
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|Medulloblastoma, SHH-activated and TP53-mutant||Disease||
|Medulloblastoma, SHH-Activated and TP53-Mutant||Disease||
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Line 3,003: Line 2,995:
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|Medulloblastoma, non-WNT/non-SHH||Disease||
|Medulloblastoma, Non-WNT/Non-SHH||Disease||
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Line 3,012: Line 3,004:
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|Medulloblastoma, histologically defined||Disease||
|Medulloblastoma, Histologically Defined||Disease||
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Line 3,021: Line 3,013:
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|Atypical teratoid/rhabdoid tumour||Disease||
|Atypical Teratoid/Rhabdoid Tumour||Disease||
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Line 3,030: Line 3,022:
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|Cribriform neuroepithelial tumour||Disease||
|Cribriform Neuroepithelial Tumour||Disease||
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Line 3,039: Line 3,031:
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|Embryonal tumour with multilayered rosettes||Disease||
|Embryonal Tumour with Multilayered Rosettes||Disease||
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Line 3,048: Line 3,040:
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|CNS neuroblastoma, FOXR2-activated||Disease||
|CNS Neuroblastoma, FOXR2-Activated||Disease||
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Line 3,057: Line 3,049:
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|CNS tumour with BCOR internal tandem duplication||Disease||
|CNS Tumour with BCOR Internal Tandem Duplication||Disease||
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Line 3,066: Line 3,058:
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|CNS embryonal tumour NEC/NOS||Disease||
|CNS Embryonal Tumour NEC/NOS||Disease||
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Line 3,084: Line 3,076:
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|Pineal parenchymal tumour of intermediate differentiation||Disease||
|Pineal Parenchymal Tumour of Intermediate Differentiation||Disease||
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Line 3,102: Line 3,094:
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|Papillary tumour of the pineal region||Disease||
|Papillary Tumour of the Pineal Region||Disease||
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Line 3,111: Line 3,103:
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|Desmoplastic myxoid tumour of the pineal region, SMARCB1-mutant||Disease||
|Desmoplastic Myxoid Tumour of the Pineal Region, SMARCB1-Mutant||Disease||
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Line 3,147: Line 3,139:
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|Hybrid nerve sheath tumours||Disease||
|Hybrid Nerve Sheath Tumours||Disease||
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Line 3,156: Line 3,148:
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|Malignant melanotic nerve sheath tumour||Disease||
|Malignant Melanotic Nerve Sheath Tumour||Disease||
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Line 3,165: Line 3,157:
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|Malignant peripheral nerve sheath tumour||Disease||
|Malignant Peripheral Nerve Sheath Tumour||Disease||
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Line 3,174: Line 3,166:
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|Cauda equina neuroendocrine tumour (previously paraganglioma)||Disease||
|Cauda Equina Neuroendocrine Tumour (Previously Paraganglioma)||Disease||
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Line 3,192: Line 3,184:
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|Solitary fibrous tumour||Disease||
|Solitary Fibrous Tumour||Disease||
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Line 3,201: Line 3,193:
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|Haemangiomas and vascular malformations||Disease||
|Haemangiomas and Vascular Malformations||Disease||
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Line 3,228: Line 3,220:
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|Intracranial mesenchymal tumour, FET::CREB fusion-positive||Disease||
|Intracranial Mesenchymal  Tumour, FET::CREB Fusion-Positive||Disease||
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Line 3,237: Line 3,229:
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|CIC-rearranged sarcoma||Disease||
|CIC-Rearranged Sarcoma||Disease||
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Line 3,246: Line 3,238:
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|Primary intracranial sarcoma, DICER1-mutant||Disease||
|Primary Intracranial  Sarcoma, DICER1-Mutant||Disease||
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Line 3,255: Line 3,247:
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|Ewing sarcoma||Disease||
|Ewing Sarcoma||Disease||
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Line 3,264: Line 3,256:
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|Mesenchymal chondrosarcoma||Disease||
|Mesenchymal Chondrosarcoma||Disease||
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Line 3,291: Line 3,283:
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|Diffuse meningeal melanocytic neoplasms: Melanocytosis and melanomatosis||Disease||
|Diffuse Meningeal Melanocytic Neoplasms: Melanocytosis and Melanomatosis||Disease||
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Line 3,300: Line 3,292:
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|Circumscribed meningeal melanocytic neoplasms: Melanocytoma and melanoma||Disease||
|Circumscribed Meningeal Melanocytic Neoplasms: Melanocytoma and Melanoma||Disease||
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Line 3,309: Line 3,301:
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|Primary diffuse large B-cell lymphoma of the CNS||Disease||
|Primary Diffuse Large B-cell Lymphoma of the CNS||Disease||
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Line 3,318: Line 3,310:
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|Immunodeficiency-associated CNS lymphomas||Disease||
|Immunodeficiency-Associated CNS Lymphomas||Disease||
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Line 3,327: Line 3,319:
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|Lymphomatoid granulomatosis||Disease||
|Lymphomatoid Granulomatosis||Disease||
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Line 3,336: Line 3,328:
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|Intravascular large B-cell lymphoma||Disease||
|Intravascular Large B-cell Lymphoma||Disease||
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Line 3,345: Line 3,337:
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|MALT lymphoma of the dura||Disease||
|MALT Lymphoma of the Dura||Disease||
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Line 3,354: Line 3,346:
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|Other low-grade B-cell lymphomas of the CNS||Disease||
|Other Low-Grade B-cell Lymphomas of the CNS||Disease||
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Line 3,363: Line 3,355:
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|Anaplastic large cell lymphoma (ALK+/ALK−)||Disease||
|Anaplastic Large Cell Lymphoma (ALK+/ALK−)||Disease||
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Line 3,372: Line 3,364:
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|T-cell and NK/T-cell lymphomas||Disease||
|T-cell and NK/T-cell Lymphomas||Disease||
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Line 3,381: Line 3,373:
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|Erdheim-Chester disease||Disease||
|Erdheim-Chester Disease||Disease||
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Line 3,390: Line 3,382:
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|Rosai-Dorfman disease||Disease||
|Rosai-Dorfman Disease||Disease||
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Line 3,399: Line 3,391:
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|Juvenile xanthogranuloma||Disease||
|Juvenile Xanthogranuloma||Disease||
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Line 3,408: Line 3,400:
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|Langerhans cell histiocytosis||Disease||
|Langerhans Cell Histiocytosis||Disease||
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Line 3,417: Line 3,409:
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|Histiocytic sarcoma||Disease||
|Histiocytic Sarcoma||Disease||
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Line 3,426: Line 3,418:
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|Germ cell tumours of the CNS||Disease||
|Germ Cell Tumours of the CNS||Disease||
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Line 3,435: Line 3,427:
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|Adamantinomatous craniopharyngioma||Disease||
|Adamantinomatous Craniopharyngioma||Disease||
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Line 3,444: Line 3,436:
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|Papillary craniopharyngioma||Disease||
|Papillary Craniopharyngioma||Disease||
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Line 3,453: Line 3,445:
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|Pituicytoma, granular cell tumour of the sellar region, and spindle cell oncocytoma||Disease||
|Pituicytoma, Granular Cell Tumour of the Sellar Region, and Spindle Cell Oncocytoma||Disease||
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Line 3,462: Line 3,454:
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|Pituitary adenoma / pituitary neuroendocrine tumour||Disease||
|Pituitary Adenoma/Pituitary Neuroendocrine Tumour||Disease||
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Line 3,471: Line 3,463:
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|Pituitary blastoma||Disease||
|Pituitary Blastoma||Disease||
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Line 3,480: Line 3,472:
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|Metastases to the brain and spinal cord parenchyma||Disease||
|Metastases to the Brain and Spinal Cord Parenchyma||Disease||
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Line 3,489: Line 3,481:
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|Metastases to the meninges||Disease||
|Metastases to the Meninges||Disease||
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Line 3,498: Line 3,490:
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|Neurofibromatosis type 1||Disease||
|Neurofibromatosis Type 1||Disease||
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Line 3,507: Line 3,499:
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|Neurofibromatosis type 2||Disease||
|Neurofibromatosis Type 2||Disease||
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Line 3,525: Line 3,517:
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|Von Hippel-Lindau syndrome||Disease||
|Von Hippel-Lindau Syndrome||Disease||
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Line 3,534: Line 3,526:
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|Tuberous sclerosis||Disease||
|Tuberous Sclerosis||Disease||
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Line 3,543: Line 3,535:
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|Li-Fraumeni syndrome||Disease||
|Li-Fraumeni Syndrome||Disease||
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Line 3,552: Line 3,544:
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|Cowden syndrome||Disease||
|Cowden Syndrome||Disease||
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Line 3,561: Line 3,553:
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|Constitutional mismatch repair deficiency syndrome||Disease||
|Constitutional Mismatch Repair Deficiency Syndrome||Disease||
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Line 3,570: Line 3,562:
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|Familial adenomatous polyposis 1||Disease||
|Familial Adenomatous Polyposis 1||Disease||
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Line 3,579: Line 3,571:
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|Naevoid basal cell carcinoma syndrome||Disease||
|Naevoid Basal Cell Carcinoma Syndrome||Disease||
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Line 3,588: Line 3,580:
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|Rhabdoid tumour predisposition syndrome||Disease||
|Rhabdoid Tumour Predisposition Syndrome||Disease||
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Line 3,597: Line 3,589:
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|Carney complex||Disease||
|Carney Complex||Disease||
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Line 3,606: Line 3,598:
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|DICER1 syndrome||Disease||
|DICER1 Syndrome||Disease||
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Line 3,615: Line 3,607:
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|Familial paraganglioma syndromes||Disease||
|Familial Paraganglioma Syndromes||Disease||
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Line 3,624: Line 3,616:
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|Melanoma-astrocytoma syndrome||Disease||
|Melanoma-Astrocytoma Syndrome||Disease||
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Line 3,633: Line 3,625:
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|Familial retinoblastoma||Disease||
|Familial Retinoblastoma||Disease||
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Line 3,642: Line 3,634:
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|BAP1 tumour predisposition syndrome||Disease||
|BAP1 Tumour Predisposition Syndrome||Disease||
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Line 3,651: Line 3,643:
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|Fanconi anaemia||Disease||
|Fanconi Anaemia||Disease||
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Line 3,660: Line 3,652:
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|ELP1-medulloblastoma syndrome||Disease||
|ELP1-Medulloblastoma Syndrome||Disease||
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Retrieved from "https://test.ccga.io/index.php/Volunteer_Assignments_and_Opportunities"