spastic paraplegia 11 (autosomal recessive) (SPG11) - 623 nt intron 25 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.72656
gtgaggatcatgagaagcctgaagtaagtacccagagaacaatagaataagtaatgaggg  c.4434+60

         .         .         .         .         .         .  g.72716
acaggaaaggctgataatcagaagtggggtgatgatgacagtgaggttccagcatgtgtt  c.4434+120

         .         .         .         .         .         .  g.72776
tccaagttcactgcaacattttgtgcttctctagcttaggctctgggccatttggtgtac  c.4434+180

         .         .         .         .         .         .  g.72836
tttcttgtgccttgacattcagtgaactcaagtgatcagagccttggtttctggttggca  c.4434+240

         .         .         .         .         .         .  g.72896
gtcacagagaaagacgctttggtggactgaccaccactgtttctttagtgccctctttag  c.4434+300

         .    g.72908
cagggaagaggg  c.4434+312

--------------------- middle of intron ---------------------
                                     g.72909      .           g.72919
                                     c.4435-311  acattccagac  c.4435-301

.         .         .         .         .         .           g.72979
agtcctttaatcagcagatcagtggagggcaatcctactctcttatgattagtacttccc  c.4435-241

.         .         .         .         .         .           g.73039
tgacttttgcatatacccccttctgtctgcttcttggtcttgtgacctgcaacactctgc  c.4435-181

.         .         .         .         .         .           g.73099
aggacagtttagaacagtcccttggttgctcattagtttgtttcatgtttgaaggctttt  c.4435-121

.         .         .         .         .         .           g.73159
caagccattttaactaattaagttgggtgacttattctaaacaggaaatatccatctgta  c.4435-61

.         .         .         .         .         .           g.73219
gtatttgtacatttgccaggtaatccaggcctagttgttattttatttatcccgtggcag  c.4435-1