Usher syndrome 1C (autosomal recessive, severe) (USH1C) - 351 nt intron 13 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.28131
gtgagtacctcggctccacgcgtgtctgtgcatgaacatcagtgtgctcaggggagtgtg  c.1085+60

         .         .         .         .         .         .  g.28191
gccaaccagaggctgcctccagaaccagtttacctggttctctcatcccctggtgggtcc  c.1085+120

         .         .         .         .         .        g.28247
tcctttatttgtagtaaagcctgtcatattatagtaactgaaacatagtctcgtat  c.1085+176

--------------------- middle of intron ---------------------
          .         .         .         .         .           g.28302
     aattgccaaggtggggttcacactcaatttagaatacaagctcggggactttgct  c.1086-121

.         .         .         .         .         .           g.28362
tgattcatcatgactagaaccatgaggcttctccccaggctggctggggctctccgatat  c.1086-61

.         .         .         .         .         .           g.28422
gcaggagatgggcctatgggggttctgactccagtaacaggcatgggggtctcattttag  c.1086-1