Meckel syndrome, type 1 (MKS1) - 255 nt intron 10 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.13686
gtaagtgtcttgctagcatagatctcttgatgcttaggcacgtgcctagatggagctgtg  c.1034+60

         .         .         .         .         .         .  g.13746
aatagtctcctccactctggtagaggccttgtctgctgtacttgggaaactcagtggtga  c.1034+120

          g.13754
gtctttcc  c.1034+128

--------------------- middle of intron ---------------------
                                         g.13755              g.13761
                                         c.1035-127  tggaaac  c.1035-121

.         .         .         .         .         .           g.13821
gcagagggttcctggccctcaaaagacttgctctcagggtgtgtaggcccctcaggattg  c.1035-61

.         .         .         .         .         .           g.13881
ggttgggtgctaagggtggtaggagaaaaagctaaaatagcttcctgttttctctcgtag  c.1035-1