Gene Location [1]
Variant Type

Significance of MYC Expression in Diseases

Diffuse Large B-Cell Lymphoma +

Medulloblastoma +

Double-Hit Lymphoma +

Hodgkin Lymphoma +

Mantle Cell Lymphoma +

Medulloblastoma, Non-WNT/Non-SHH +

Burkitt Lymphoma +

Central Nervous System Embryonal Neoplasm +

Central Nervous System Ganglioneuroblastoma +

Central Nervous System Neuroblastoma +

Chronic Lymphocytic Leukemia +

Follicular Lymphoma +

High Grade B-Cell Lymphoma, Not Otherwise Specified +

Medulloblastoma, SHH-Activated +

Medulloepithelioma +

Triple-Hit Lymphoma +

Anaplastic Astrocytoma +

Anaplastic Astrocytoma, IDH-Mutant +

Anaplastic Ependymoma +

Anaplastic Oligodendroglioma +

Anaplastic Oligodendroglioma, IDH-Mutant And 1p/19q-Codeleted +

Anaplastic Pleomorphic Xanthoastrocytoma +

Atypical Teratoid/Rhabdoid Tumor +

B-Cell Non-Hodgkin Lymphoma +

Central Nervous System Neoplasm +

Desmoplastic/Nodular Medulloblastoma +

Diffuse Glioma +

Diffuse Large B-Cell Lymphoma, Not Otherwise Specified +

Diffuse Midline Glioma, H3 K27M-Mutant +

Embryonal Tumor With Multilayered Rosettes, C19MC-Altered +

Embryonal Tumor With Multilayered Rosettes, Not Otherwise Specified +

Ependymoma +

Ependymoma, RELA Fusion-Positive +

Glioblastoma +

Hairy Cell Leukemia +

High Grade B-Cell Lymphoma With MYC And BCL2 And/Or BCL6 Rearrangements +

High-Grade Glioma, NOS +

Intraocular Lymphoma +

Large Cell/Anaplastic Medulloblastoma +

Lymphoma +

Lymphoplasmacytic Lymphoma +

Malignant Glioma +

Marginal Zone Lymphoma +

Mature B-Cell Lymphoma/Leukemia +

Mature B-Cell Non-Hodgkin Lymphoma +

Medulloblastoma With Extensive Nodularity +

Medulloblastoma, WNT-Activated +

Neuroblastoma +

Non-Hodgkin Lymphoma +

Peripheral T-Cell Lymphoma +

Pineoblastoma +

Primary Mediastinal B-Cell Lymphoma +

Small Intestinal Lymphoma +

Small Lymphocytic Leukemia +

Small Lymphocytic Lymphoma +

Solid Neoplasm +

Transformed Non-Hodgkin Lymphoma +


1. Hart R and Prlic A. Universal Transcript Archive Repository. Version uta_20180821. San Francisco CA: Github;2015. https://github.com/biocommons/uta

2. The UniProt Consortium. UniProt: a worldwide hub of protein knowledge. Nucleic Acids Research. 2019;47:D506-D515.

3. Liu X, Wu C, Li C, and Boerwinkle E. dbNSFP v3.0: A one-stop database of functional predictions and annotations for human nonsynonymous and splice site SNVs. Human Mutation. 2015;37:235-241.

Liu X, Jian X, and Boerwinkle E. dbNSFP: A lightweight database of human nonsynonymous SNPs and their functional predictions. Human Mutation. 2011;32:894-899.

4. The AACR Project GENIE Consortium. AACR Project GENIE: powering precision medicine through an international consortium. Cancer Discovery. 2017;7(8):818-831. Dataset Version 8. This dataset does not represent the totality of the genetic landscape; see paper for more information.

5. All assertions and clinical trial landscape data are curated from primary sources. You can read more about the curation process here.