spastic paraplegia 7 (pure and complicated autosomal recessive) (SPG7) - 658 nt intron 14 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.49799
gtgaggagcagcggcgcgggccctggaggtttcagagcgcttttccctgcatgactcctt  c.1936+60

         .         .         .         .         .         .  g.49859
ctgttccagtgcatgccatggggtgaatctggtgtagacgtagctttgaatttattaagt  c.1936+120

         .         .         .         .         .         .  g.49919
attttgtaaaagataagttgtggtcataagagagttggagctaagcaagacttcttagat  c.1936+180

         .         .         .         .         .         .  g.49979
aatttaattggacaaaaacttaacctatatgccaactctagacacatttaattggttaat  c.1936+240

         .         .         .         .         .         .  g.50039
tgttggtaatggctacaggaaacggaataaaattgaagcggcttcattgttctgaagcca  c.1936+300

         .         .           g.50068
ttactgcactgggatatccagagagctga  c.1936+329

--------------------- middle of intron ---------------------
                   g.50069              .         .           g.50097
                   c.1937-329  aggagggtcccgggggcccctgggctcca  c.1937-301

.         .         .         .         .         .           g.50157
ggtccatgggtttgcctcgcataggcctgggcttgtgcttgagaactgccatgcagtgag  c.1937-241

.         .         .         .         .         .           g.50217
ctccagtatgcccccgggttctagatttccaaataaaagagcatttcggaaagttttaag  c.1937-181

.         .         .         .         .         .           g.50277
actctcttaaggaacagtggtgaggtgccaacgtcctcactgtccagcttcacggtgggt  c.1937-121

.         .         .         .         .         .           g.50337
cctcgggaggaaggggatggaggtggtgctgcctcagtgctctgaccgggacacctgggg  c.1937-61

.         .         .         .         .         .           g.50397
cccagcactgctctgcgcctgcagtgctgaggatgcctctgtctcgaccccgccctccag  c.1937-1