Individuals with missense variants that affect the NF1 codons 844–848 have a statistically higher risk of developing spinal neurofibromas, plexiform neurofibromas, and optic pathway gliomas, whereas the pathogenic recurrent missense variants of p.Met1149, p.Arg1276, and p.Lys1423 are correlated with the Noonan-like phenotype [12]. This evidence concerns the gene NF1 and Spinal neurofibroma.