Fig. 2: Single-nucleotide mutations in FGFR1/2.
From: Activation of FGFR genes by genetic and epigenetic alterations in uterine leiomyomas
a Altogether eight single-nucleotide mutations were found in FGFR1/2 in the Finland Myoma Study Collection. b, c Distribution of single-nucleotide mutations in FGFR1/2 in the COSMIC database of cancer mutations and the Sanger validated mutations in FGFR1/2 mutation hotspots found in our UL sample set. The domain information was obtained from the InterPro database [30].
