Overview

FGFR1OP2 is altered in 0.14% of all cancers with breast invasive ductal carcinoma, colon adenocarcinoma, dysembryoplastic neuroepithelial tumor, high grade ovarian serous adenocarcinoma, and invasive breast carcinoma having the greatest prevalence of alterations [3].

The most common alterations in FGFR1OP2 are FGFR1OP2-FGFR1 Fusion (0.22%) and FGFR1OP2-ETV6 Fusion (0.01%) [3].

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. 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.

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