spastic paraplegia 7 (pure and complicated autosomal recessive) (SPG7) - 525 nt intron 15 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.50624
gtgagtcggctctggccacaccgctgccctctgtgctccccggggagggagtccctgggt  c.2103+60

         .         .         .         .         .         .  g.50684
ctaccacacaagggtcgcccacggccgccccagcggagctcagctgcaggccccacctgg  c.2103+120

         .         .         .         .         .         .  g.50744
gtttcttccttctgggctctgctgtagttcccacctgtggagtattttcttctcaaatga  c.2103+180

         .         .         .         .         .         .  g.50804
ggacatagatgctcctaatgaaattatagatgtgaatctgggaagaatatcaaataaata  c.2103+240

         .         .     g.50827
caccgagcaatagacccagggcc  c.2103+263

--------------------- middle of intron ---------------------
                          g.50828       .         .           g.50849
                          c.2104-262  cacatgtccttcagactgggcc  c.2104-241

.         .         .         .         .         .           g.50909
aggaagggccgatgtgtgcctgtgaggcagctgtgggtgggtgtgggtgggtgggctggc  c.2104-181

.         .         .         .         .         .           g.50969
atgcggagccctgctttcctggcactggtcacaggggcaggagaccacctgtcggctgag  c.2104-121

.         .         .         .         .         .           g.51029
gagtcctgttcctcctgggaggggaaaggccgtgttcccagtctgccatttcttttctgt  c.2104-61

.         .         .         .         .         .           g.51089
gctttggtgctggagccaggcggccagccttgcccctgacacagttccctccactcacag  c.2104-1