Meckel syndrome, type 1 (MKS1) - 537 nt intron 15 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.17581
gtgacttttgtctttggagtgacttcacgctgagaacttatggtcctgtccttctgtagg  c.1483+60

         .         .         .         .         .         .  g.17641
aggtgggatctgggtcaagaccccttagttgtgcattgcttcagtattaaccccttcctt  c.1483+120

         .         .         .         .         .         .  g.17701
cctgtggcttaagctggaagtcatgaccacattttgaatcaggttccaatatctacactg  c.1483+180

         .         .         .         .         .         .  g.17761
ctatcgtaggaggtctctggaaaatagtataattagagatttcccctggttcccatcaga  c.1483+240

         .         .           g.17790
ataactggctctttcccccatcactgaag  c.1483+269

--------------------- middle of intron ---------------------
                    g.17791             .         .           g.17818
                    c.1484-268  gcctcagtaatcagatgtggggaggatt  c.1484-241

.         .         .         .         .         .           g.17878
cacagtaagcatataagaccgccgcttctcaaatgaggttggaatgttccctggtttagt  c.1484-181

.         .         .         .         .         .           g.17938
tgggggagcccaatagcccagtattagccttgaggtaatagagtctgggtgatggaataa  c.1484-121

.         .         .         .         .         .           g.17998
ggtttccccaacagaactgcgcttcccaagaatgggaataagaatgggggtgaggccagc  c.1484-61

.         .         .         .         .         .           g.18058
atggtgcgggggtgtctagagagagcagaaacctgaggctgtcccaatggcatgccacag  c.1484-1