Usher syndrome 1C (autosomal recessive, severe) (USH1C) - 205 nt intron 06 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.22461
gtgagaggcccctcctctgcaggccaactcttccctgtgggcccaggatcctggtacagc  c.521+60

         .         .         .         .     g.22504
cctggggtccggctcccaccatgccagccctgcttctgggcca  c.521+103

--------------------- middle of intron ---------------------
       g.22505      .         .         .         .           g.22546
       c.522-102  gtggaggctggaggctctagacatggtggatctggatgtggg  c.522-61

.         .         .         .         .         .           g.22606
gcctggttcctcaaacgtctctcgctaaccaccctcccatctattttcccttcccatcag  c.522-1