spastic paraplegia 11 (autosomal recessive) (SPG11) - 380 nt intron 12 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.46011
gtaggtaaaggtgagactacatagtatacattttctagaaagcctgggtgaaaaacttgg  c.2316+60

         .         .         .         .         .         .  g.46071
aagaaaaccttggaagaaaaaccttaagtaattttaatgttcaactaatatctaataagt  c.2316+120

         .         .         .         .         .         .  g.46131
aaaagtgtgacaaccccttcatctttttttccccttcatctttcttcaatgactatttta  c.2316+180

         .  g.46141
catttgtggc  c.2316+190

--------------------- middle of intron ---------------------
                                      g.46142     .           g.46151
                                      c.2317-190  aaaagaaaat  c.2317-181

.         .         .         .         .         .           g.46211
ttgtgttaacatacattaactcaaatgttcaaaatataattcttgaatggcatattatct  c.2317-121

.         .         .         .         .         .           g.46271
catgactttttttaataatctttaattcccagcactaccttatttgataatctcatgaca  c.2317-61

.         .         .         .         .         .           g.46331
ttttttgcaaaagtgcttgattttttgtaaagtcactgctttaattactttttattcaag  c.2317-1