Usher syndrome 1C (autosomal recessive, severe) (USH1C) - 566 nt intron 17 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.39072
gtaacagagcccttctttccacatagaccctcctgctgtcttcagaatgacccactgtgg  c.1530+60

         .         .         .         .         .         .  g.39132
ggacagcgggaggtgagatgacaactagcaaacgtcactagcctcacagtgcccatccac  c.1530+120

         .         .         .         .         .         .  g.39192
tgtccaggcccacccctaccaccccactcccctcttgaggaggagggatatgtctgtatt  c.1530+180

         .         .         .         .         .         .  g.39252
tctgggtatactcccagagtgatctctaagtcccagctcatctgcgatagtctcagttag  c.1530+240

         .         .         .         .     g.39295
gcctgttgtcctggcatcatgactaagagtcccccttacactc  c.1530+283

--------------------- middle of intron ---------------------
     g.39296        .         .         .         .           g.39338
     c.1531-283  tcaagggcattccagtttagagaatgaactctgtgaacacctt  c.1531-241

.         .         .         .         .         .           g.39398
accacccacagatggcataacttggggctcttctgcatttgggcactccctaacagcagc  c.1531-181

.         .         .         .         .         .           g.39458
ctagtatggcctcagctgggcatccaggtggcagaggaatggcgccccatggttctgatg  c.1531-121

.         .         .         .         .         .           g.39518
taagggtggtgggtctccagtagcaagagaaacagattagaagagcatagtgctcgctgt  c.1531-61

.         .         .         .         .         .           g.39578
attgtgaagtggagctctaagcagagtgacaattacagaacttccttgcaacacccccag  c.1531-1