Usher syndrome 1C (autosomal recessive, severe) (USH1C) - 311 nt intron 07 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.22724
gtaagggccagacctcctgtgatggggtttgggtggggtcatcttcaaggaggggtggcc  c.579+60

         .         .         .         .         .         .  g.22784
ggtcctgaagggagggcttgctctagagatgcaccctcaggggcttcacacaggctccca  c.579+120

         .         .         .        g.22820
gggcagccagcacaccgctgtggggcagcagccctc  c.579+156

--------------------- middle of intron ---------------------
              g.22821         .         .         .           g.22855
              c.580-155  ggccaggcccagctggtgcagacacatccccaggg  c.580-121

.         .         .         .         .         .           g.22915
acggaatgatgatctggctggcgtgagttcagcagtgctcgccctgcagatcccacaagc  c.580-61

.         .         .         .         .         .           g.22975
tcaagaggccgcttgcacgcatgtggacactccgtgattctgcttctatctctctttcag  c.580-1