Usher syndrome 1C (autosomal recessive, severe) (USH1C) - 182 nt intron 05 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.22254
gtgagtgaggccagagcagggcagtactccataacggtgggagggagggagggcggggga  c.496+60

         .         .         .   g.22285
gcagggcagtactccatgacggtgggaggga  c.496+91

--------------------- middle of intron ---------------------
                   g.22286    .         .         .           g.22316
                   c.497-91  gggagggcgggggagcaggtcagtactccat  c.497-61

.         .         .         .         .         .           g.22376
gacggtgggagggagggagggcgggggagctgtcctaacccctgtgcctttctcccgcag  c.497-1