Usher syndrome 1C (autosomal recessive, severe) (USH1C) - 403 nt intron 21 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.47538
gtaagagatgacgcttctctcctggacaagtaaccccaggaacagggcagtgtgggggtt  c.2226+60

         .         .         .         .         .         .  g.47598
agagggtttgatagtggtgcattctgggccttggggtcctgggatgaggtggggcacaga  c.2226+120

         .         .         .         .         .         .  g.47658
ggagccccagtgatgccccagctgctcttcccacgaagattccttccaaagggcactcca  c.2226+180

         .         .    g.47680
gtgtgaactgtatggtgcacat  c.2226+202

--------------------- middle of intron ---------------------
                           g.47681      .         .           g.47701
                           c.2227-201  gcacgtgtgtgtgtccactgt  c.2227-181

.         .         .         .         .         .           g.47761
ccccatggggcctgggacccccagttgaagaccagtaggggtggggctgggcacggtccc  c.2227-121

.         .         .         .         .         .           g.47821
cttgcccatgtgctctgtggggcccagtgtcccataggtgcctggattccccttccagcc  c.2227-61

.         .         .         .         .         .           g.47881
ctaccccaagcgccatccttcaggccagctcaaagcttcccactgtctttttctctctag  c.2227-1