Usher syndrome 1C (autosomal recessive, severe) (USH1C) - 1132 nt intron 19 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.43647
gtaagccccttgggtcccctccaggttgtctctagaggagcagaccagggctacctcccc  c.2133+60

         .         .         .         .         .         .  g.43707
tgggctctgctgtctctggagggcaagtgaggtgggacaaaaatgcagatcacagatgcc  c.2133+120

         .         .         .         .         .         .  g.43767
atctcttaaccttcttattggccaagagatgaggccacatgggtgtaagtggatgttgac  c.2133+180

         .         .         .         .         .         .  g.43827
atgaccagtggaatttctgttccccacttgactgaacagcctggagctctgtctaaaagt  c.2133+240

         .         .         .         .         .         .  g.43887
aataatgatcgctacgacctgtgaagagcctactatataccaggctctgcatggcctcaa  c.2133+300

         .         .         .         .         .         .  g.43947
ttaatcttcacagcaggactgtgagatggttcctgtggtcatcctgtttaacactcgagg  c.2133+360

         .         .         .         .         .         .  g.44007
aaagggaggtttagagaggttaccagaggggcaccaggttccccaggcagagcctggact  c.2133+420

         .         .         .         .         .         .  g.44067
taatacttaccctcatgcctttcatactccaaagcccacgctgttaccctcgttgccatc  c.2133+480

         .         .         .         .         .         .  g.44127
ttgccaaaacctacagagattccaggtgccctggcccctgccctaaggcctgttgtggcc  c.2133+540

         .         .        g.44153
tggcatgaaacaccctcagatgggaa  c.2133+566

--------------------- middle of intron ---------------------
                      g.44154           .         .           g.44179
                      c.2134-566  actggccagagcaggttcactccctt  c.2134-541

.         .         .         .         .         .           g.44239
tctccaacttacttctcacctctcactgtgactggaagtctgaggtgtggtcctggggaa  c.2134-481

.         .         .         .         .         .           g.44299
gtgagaaatgtccgccagtctcagttactgacggctaagggagctgggattcgtgtgcac  c.2134-421

.         .         .         .         .         .           g.44359
ctcccagaggtgccgaccactggctggcctcccatgcacagtgagaagacagtcatgtca  c.2134-361

.         .         .         .         .         .           g.44419
gaattttaacttccctttcaaggaaactctatccaaatgtcagggcaggacagctgagat  c.2134-301

.         .         .         .         .         .           g.44479
atttattttgggccttaactgtcccgtcagctccccagagagcaaagtttttgctcctgg  c.2134-241

.         .         .         .         .         .           g.44539
gacagcctgcggatgcatccatgtcatgttctctggctaatatcaaggggtggtgtctgc  c.2134-181

.         .         .         .         .         .           g.44599
ttgacaacaactgggtagcatctttgggcattgagcaggcctttaacgtaagccagactg  c.2134-121

.         .         .         .         .         .           g.44659
ctcggggagggacattggcacggcagccccagactggcaggcccgaagcctggcaccagg  c.2134-61

.         .         .         .         .         .           g.44719
gggcagccaagacctattggtaacatccaatgtggaacttttttttttttcctctggcag  c.2134-1