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. Author manuscript; available in PMC: 2011 Dec 8.
Published in final edited form as: Hum Mutat. 2009 Sep;30(9):E880–E890. doi: 10.1002/humu.21075

Figure 4.

Figure 4

Map of FLCN amino acid and nucleotide sequences (NM_144997.5) including the intron-exon boundaries (shown in blue). The position of the 53 unique FLCN mutations is shown in red. The number in red corresponds to the variant ID (FLCN_00001 to FLCN_00053) in the FLCN mutation database. Splice site mutations are marked by green boxes and the affected splice site is marked by a heavy red bar. The FLCN coding sequence and its deduced amino acid sequence are obtained using NCBI ORF Finder (Open Reading Frame Finder).