Usher syndrome 1C (autosomal recessive, severe) (USH1C) - 331 nt intron 22 reference sequence

(intronic numbering for coding DNA Reference Sequence)

         .         .         .         .         .         .  g.47995
gtacctgggcatgtggaggccggtgggccgccatccctctctgtgcctgcccctcctccc  c.2280+60

         .         .         .         .         .         .  g.48055
ttggtctcctgcctctactctcaaggtcactcctgggtggtctctcaggtccccactgtc  c.2280+120

         .         .         .         .        g.48101
ctcccctctcccacggagacgcccctctgttgtagggccgcatacc  c.2280+166

--------------------- middle of intron ---------------------
   g.48102          .         .         .         .           g.48146
   c.2281-165  caggccccacttggcaccaaggctgcgttttctccagatggcact  c.2281-121

.         .         .         .         .         .           g.48206
gccggtgaccccatggcttcttccactcttactgtggctctgtcaagagactccttggtg  c.2281-61

.         .         .         .         .         .           g.48266
cccaggtgtccacaggctgctgtctgcttggctccctaaggcctgttttcctctaaccag  c.2281-1