Meckel syndrome, type 1 (MKS1) - 389 nt intron 06 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.10407
gtgagtggcgcttctcactgccagcttagagcctcatccttttctcctctcaccagctct  c.720+60

         .         .         .         .         .         .  g.10467
ccccttcctgttattatcatcctaggttataggggagggagggactttttcttccttctc  c.720+120

         .         .         .         .         .         .  g.10527
ttcttagttatgagtgaagcttctcactgccaactcagatcctcatcttcttctcctctc  c.720+180

         .       g.10542
accagctatcccctt  c.720+195

--------------------- middle of intron ---------------------
                                   g.10543        .           g.10556
                                   c.721-194  cctgttatcatcct  c.721-181

.         .         .         .         .         .           g.10616
gggttataggagaggaagggactttttcttccttttttttcttagttgtacttggaagaa  c.721-121

.         .         .         .         .         .           g.10676
agttttaccatgacagctctccctatagcctctgttctctcccctgcagtgggctcagta  c.721-61

.         .         .         .         .         .           g.10736
tctcttcttgtttccctgaaggaccattgacctcaaccttggtgttttcctgatttctag  c.721-1