Meckel syndrome, type 1 (MKS1) - 674 nt intron 07 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.10901
gtgaggagaggaagaaaggggtagtggagactggcattccttcccttggttgcacttttt  c.825+60

         .         .         .         .         .         .  g.10961
gtccctagtcaactagactgtcagaaagtccttcatctgttctaacttttacattcccag  c.825+120

         .         .         .         .         .         .  g.11021
gcaatggttcgtattctgttccaagtcatagggccttagaaaaccagggactcctttctc  c.825+180

         .         .         .         .         .         .  g.11081
agaaaatgtgcaactgcaccaatttgaaagggatcacttcagtggtacagttaaatgaca  c.825+240

         .         .         .         .         .         .  g.11141
gtgattctctgtgctgctgaatgtaggacctgaccagaacagagtggggtgaactcagcc  c.825+300

         .         .         .         g.11178
aggcttttcctgtgggctgactgttcctcatctctgt  c.825+337

--------------------- middle of intron ---------------------
            g.11179           .         .         .           g.11215
            c.826-337  atcttggaaatgacagaaatgtaaattagaaattatc  c.826-301

.         .         .         .         .         .           g.11275
tggcccaacctgtccatttttcaggtgagagaactgggtggcaggaatgttgtgccttac  c.826-241

.         .         .         .         .         .           g.11335
agtttgactgtaacttcaagccagaaatgggcccagaacctatactttctgagtctagtc  c.826-181

.         .         .         .         .         .           g.11395
tggtgccctctctgctttacccttttgtttctctctcctggtcgtcaatacagccacttt  c.826-121

.         .         .         .         .         .           g.11455
tatcatcatatactttagtgaggtgtatggcccctgatcgctcatccctgggctgggagc  c.826-61

.         .         .         .         .         .           g.11515
tatcccagggcccatctctcattattagagttgctcctttctgtggttttgaccttacag  c.826-1