spastic paraplegia 11 (autosomal recessive) (SPG11) - 388 nt intron 09 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.39506
gtaagaatagcagctaggaagggggcaattctactgttcctgtgtcagaacagatacaag  c.1891+60

         .         .         .         .         .         .  g.39566
tgctgctattgggtgacacagcataaaccagtggcacgccatttactacatttgggtaag  c.1891+120

         .         .         .         .         .         .  g.39626
gtcagtgtgtagttgagtaagtgaaatgggttttgatactgagaaagttggtagaaagac  c.1891+180

         .      g.39640
ccaggactaatcat  c.1891+194

--------------------- middle of intron ---------------------
                                  g.39641         .           g.39654
                                  c.1892-194  gaaggacaagaaaa  c.1892-181

.         .         .         .         .         .           g.39714
ggaaagggttatattaaaatacagagctacttacttgtaaaaaggaaaatcctcagacat  c.1892-121

.         .         .         .         .         .           g.39774
attgtttgaaatttaaaaataccaagtttgaattttgactttctttagaattctttataa  c.1892-61

.         .         .         .         .         .           g.39834
cagctcatggtttatatttacacacacacacacaaattggcacattggtattttccatag  c.1892-1