Gene Location [1]
Variant Type
Deletion - In frame

NOTCH2 Deletion is present in 0.03% of AACR GENIE cases, with glioblastoma, lung adenocarcinoma, adenocarcinoma of unknown primary, anaplastic astrocytoma, and colon adenocarcinoma having the greatest prevalence [4].

Top Disease Cases with NOTCH2 Deletion

Significance of NOTCH2 Deletion in Diseases

Anaplastic Astrocytoma +

Glioblastoma +

Lymphoma +

Non-Small Cell Lung Carcinoma +

Colorectal Carcinoma +

Malignant Solid Tumor +

Bladder Carcinoma +

Breast Carcinoma +

Head And Neck Carcinoma +

Melanoma +

Ovarian Carcinoma +

Pancreatic Carcinoma +

Sarcoma +


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.