Meckel syndrome, type 1 (MKS1) - 338 nt intron 12 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.16153
gtatggagaatgagagcgggtatctggaagggaatgagatctgctcctgggatggcattt  c.1171+60

         .         .         .         .         .         .  g.16213
gaggttttatcaggccaagtgctgtgcgccctggggaggattccagagttgggtgacttg  c.1171+120

         .         .         .         .           g.16262
tgtgtgggttctacagggccacctggtccggagatcctgtctgtctttt  c.1171+169

--------------------- middle of intron ---------------------
          g.16263              .         .         .         .           g.16311
          c.1172-169  tgagcatggcagcagcttgtatttgggtgtccttttgcatctcagactc  c.1172-121

.         .         .         .         .         .           g.16371
ctatttcccacctgggtgataatttttctttttcccttgtgaagataaccttgtcattgg  c.1172-61

.         .         .         .         .         .           g.16431
ccacaaggagaacagattccaagggaggccttgcccaccctatgacactcctttttatag  c.1172-1