Associated Genetic Biomarkers

Overview

Gene Location [1]
3p25.2
Pathway
MAP kinase signaling
Gene
RAF1

RAF1 Mutation is present in 0.83% of AACR GENIE cases, with colon adenocarcinoma, lung adenocarcinoma, cutaneous melanoma, endometrial endometrioid adenocarcinoma, and bladder urothelial carcinoma having the greatest prevalence [4].

Top Disease Cases with RAF1 Mutation

Significance of RAF1 Mutation in Diseases

Malignant Solid Tumor +

Non-Small Cell Lung Carcinoma +

Melanoma +

Non-Hodgkin Lymphoma +

Ovarian Carcinoma +

Pancreatic Carcinoma +

Colorectal Carcinoma +

Esophageal Carcinoma +

Glioma +

Breast Carcinoma +

Adenocarcinoma Of The Gastroesophageal Junction +

Histiocytic And Dendritic Cell Neoplasm +

Neuroblastoma +

Cutaneous Melanoma +

Endometrial Carcinoma +

Malignant Uterine Neoplasm +

Gastric Adenocarcinoma +

Gastric Carcinoma +

Urothelial Carcinoma +

Bladder Carcinoma +

Lung Carcinoma +

Low Grade Glioma +

Soft Tissue Sarcoma +

Hepatobiliary Neoplasm +

Malignant Hepatobiliary Neoplasm +

Bile Duct Carcinoma +

Bronchogenic Carcinoma +

Cervical Carcinoma +

Embryonal Rhabdomyosarcoma +

Esophageal Squamous Cell Carcinoma +

Gallbladder Carcinoma +

Gastrointestinal Stromal Tumor +

Head And Neck Carcinoma +

Hepatocellular Carcinoma +

Lip And Oral Cavity Carcinoma +

Malignant Laryngeal Neoplasm +

Malignant Peripheral Nerve Sheath Tumor +

Malignant Salivary Gland Neoplasm +

Multiple Myeloma +

Nasal Cavity And Paranasal Sinus Carcinoma +

Nasopharyngeal Carcinoma +

Neurofibromatosis Type 1 +

Oropharyngeal Carcinoma +

Poorly Differentiated Thyroid Gland Carcinoma +

Renal Cell Carcinoma +

Rhabdoid Tumor +

Schwannoma +

Squamous Cell Lung Carcinoma +

Thyroid Gland Carcinoma +

Thyroid Gland Undifferentiated (Anaplastic) Carcinoma +

References

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 6. 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.