Meckel syndrome, type 1 (MKS1) - 675 nt intron 14 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.16772
gtaaccgctcgtctctgcccttctgtggcccacatgccctaggccctaagaacaagacta  c.1349+60

         .         .         .         .         .         .  g.16832
acactcgaatgcttctggtgaggggtggagataattgggaattggaaatgtttggcttga  c.1349+120

         .         .         .         .         .         .  g.16892
aagagttcctgttcctctgaggactttctgcccccctccattagcgacaatgacgtggcc  c.1349+180

         .         .         .         .         .         .  g.16952
ttggcactgacttcctgacagtctctccatgtgcttcatgctcctctgattggactcagg  c.1349+240

         .         .         .         .         .         .  g.17012
gtgagaagctgtatggcaaaattggctcatagcatatgtgtattgaatgaatcagcattc  c.1349+300

         .         .         .          g.17050
agtttggaataaaagcatctgtcttttactgtgtgcca  c.1349+338

--------------------- middle of intron ---------------------
           g.17051            .         .         .           g.17087
           c.1350-337  ggcattgtgccatacttctcacttaattctcccagtc  c.1350-301

.         .         .         .         .         .           g.17147
actctgtgaggtgcaggtggtattatttccattttactagatgaggagaatgagcttcag  c.1350-241

.         .         .         .         .         .           g.17207
agaggttaagaaacctgtcctgggtatgcaggtaataactggcagagcggaaatttgaat  c.1350-181

.         .         .         .         .         .           g.17267
ttctccctgattgatttccatacaggtgctatgggtaaccatgataacctgcaccagagg  c.1350-121

.         .         .         .         .         .           g.17327
ccaggtcatcaccagaccaggtgttttagctgagtctaggcctgtgtcattgctggggag  c.1350-61

.         .         .         .         .         .           g.17387
tcagtgaggggccacatgccctttctggacctggccccagtcttctcttcccttgcgcag  c.1350-1